Therapeutic Targeting of Notch Signaling Pathway in Hematological Malignancies

Claudia Sorrentino1, Antonio Cuneo1,2 and Giovanni Roti1.

1 University of Parma, Department of Medicine and Surgery, Parma, 43126, Italy.
2 University of Ferrara, Department of Medical Sciences, Ferrara, 44121, Italy.

Correspondence to: Giovanni Roti. University of Parma, Department of Medicine and Surgery, Parma, 43126, Italy. E-mail:

Published: July 1, 2019
Received: March 3, 2019
Accepted: May 18, 2019
Mediterr J Hematol Infect Dis 2019, 11(1): e2019037 DOI 10.4084/MJHID.2019.037

This is an Open Access article distributed under the terms of the Creative Commons Attribution License
(, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The Notch pathway plays a key role in several processes, including stem-cell self-renewal, proliferation, and cell differentiation. Several studies identified recurrent mutations in hematological malignancies making Notch one of the most desirable targets in leukemia and lymphoma. The Notch signaling mediates resistance to therapy and controls cancer stem cells supporting the development of on-target therapeutic strategies to improve patients’ outcome. In this brief review, we outline the therapeutic potential of targeting Notch pathway in T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and mantle cell lymphoma..


Notch pathway comprises a family of single-pass transmembrane receptors, their ligands, and coactivators that regulate evolutionarily conserved signaling that controls development and tissue homeostasis[1,2] in all metazoan organisms. Mammalian NOTCH receptors (NOTCH 1-4) are pre-processed during maturation by a furin-like protease (S1), leading to the formation of two, non-covalently associated subunits. In non-malignant cells, canonical Notch signaling is initiated by cell-to-cell contact of the Notch extracellular domain (NECD) to a ligand of the Delta-like (DLL1, DLL3, DLL4) and Jagged family (JAG1, JAG2), expressed on the cellular surface of the neighboring cell. This receptor-ligand interaction mediates a sequence of two proteolytic cleavages in the Notch transmembrane subunit. The first, resolved by ADAM-10 or ADAM-17 metalloproteases, occurs within a juxtamembrane negative regulatory region (NRR) at a site that is protected in the inactive state (S2).[3-5] This cleavage generates a trans-membrane intermediate that is the substrate for a secondary cleavage (S3) by the γ-secretase, an event that releases the intracellular domain of NOTCH (ICN, NICD).[6] ICN moves to the nucleus, complexes with the DNA-binding factor RBPJ, and recruits coactivator of the Mastermind-like (MAML) family. The resulting macromolecules complex activates genes transcription but is usually short-lived because the C-terminal portion of ICN (PEST, peptide sequence that is rich in proline (P), glutamic acid (E), serine (S), and threonine (T)) is recognized by an E3 ubiquitin ligase and degraded.[7]
The NOTCH proteins have several functional domains organized in modules. The NECD N- terminal domain is responsible for ligand binding through EGF-like Ca2+ dependent repeats, followed by three LNR (Lin12/Notch) units. Next to the LNR region lays the juxtamembrane heterodimerization domain (HD), a linker between the extracellular tail and ICN. LNR and HD modules constitute the negative regulatory region (NRR) that prevents ADAM-10/17 cleavage of mammalian Notch in the ligand's absence (Figure 1A).[3-5,8]

Figure 1 Figure 1. A) The schema shows domain organization of NOTCH protein (NOTCH1 shown). The extracellular domain of NOTCH receptor consists of multiple EGF repeats followed by the NRR (negative regulatory region), which consists of three LNR (Lin-12 and Notch repeats) domains and HD (heterodimerization domain). The intracellular domain of NOTCH receptor consists of a membrane proximal RAM (RBPJ associated molecule) domain, ANK (ankyrin repeats), and a C- terminal TAD (trans-activation domain) comprised of three NLS (nuclear localization sequences) and degron-containing PEST (rich in proline, glutamate, serine, and threonine) sequence.
B) An overview of Notch1 signaling and proteolytic processing in the presence of SERCA inhibition. NOTCH1 receptor is a cell surface protein. In physiological condition interaction with the Notch ligand, such as JAG1-2 or Dll-4, initiates proteolytic cleavage at the extracellular site by a metalloprotease (TACE) followed by a γ-secretase (GSI) cleavage, resulting in the release of ICN1. ICN1 is then translocated into the nucleus where it interacts with CSL and recruits coactivators to form a transcription-activating complex. In the presence of NOTCH1 mutations, ICN1 is constitutively active and avoids activation through ligand interaction. Inhibition of the sarco/endoplasmic reticulum Ca2+ ATPase (SERCA) leads to alteration in NOTCH1 trafficking causing a loss of NOTCH1 proteins on the surface of the cells and an accumulation of full-length polypeptides on the endoplasmic reticulum/Golgi region. The consequent lack of TACE and GSI substrate causes a reduction in ICN1 level.

While oncogenic alterations in the Notch signaling have been described in almost all human cancers,[3,9] the majority of the recurrent somatic mutations of NOTCH proteins are observed in the NOTCH1 gene.
The role of NOTCH1 in the pathogenesis of T-cell acute lymphoblastic leukemia (T-ALL), was first investigated in 1991.[1] Ellisen and colleagues described a chromosome translocation, t(7;9)(q34;q34), that juxtaposes the T-cell receptor-β to the active form of ICN1 in T-ALL.[10] This fusion creates an oncogenic Notch1 signaling in leukemia cells. Similarly, to the translocation, activating NOTCH1 mutations generate ligand independent or proteasome resistant ICN1 peptides that sustain T-cell transformation, leukemia growth, or resistance to therapy.[10] In T-ALL, 
NOTCH1 mutations cluster in two different but not mutually exclusive hotspots.[11,12] The first comprises a single amino acid substitution and in-frame insertion in the extracellular NRR. To this class also belongs the rare in-frame insertion in the juxtamembrane extracellular domain (JME). Within the NRR module, most of these mutations occur in the HD domain, and they are defined as type 1A and 1B.[13] Briefly, HD mutations cause ligand-independent Notch conformational changes that constitutively activate ICN1. The second hotspot of NOTCH1 mutations comprises small insertion/deletion in the exon 34 (PEST domain). These genetic lesions truncate NOTCH1 C-terminal generating a long-lived ICN1 caused by the consequent loss of the “degron” recognition site of the PEST unit.[11,14]
Recently, NOTCH1 emerged as one of the most frequently mutated genes (~5-20%) in chronic lymphocytic leukemia (CLL), where it may represent an early driver lesion in a proportion of cases.[15,16] Most of these mutations, ~80%, are a 2-bp deletion in exon 34 that generates a premature stop codon (P2514fs*4), that truncates the PEST region. Similarly to T-ALL, these mutations cause an over-activation of Notch1 signaling because of the lack of its degradation.[17] Interestingly Kridel and colleagues reported a similar pattern of mutations within the PEST domain in mantle cell lymphoma (MCL).[18,19] Furthermore, 50% of NOTCH1 wild-type CLL cases express ICN1 suggesting that the activation through the canonical Notch signaling is required for leukemia growth in this disease.[20] However, in CLL and MCL, mutations in NOTCH1 are associated with a worse prognosis.[17,21-23] In addition to these observations, Schmitz and colleagues recently described a genetic framework for diffuse large B-cell lymphoma (DLBCL) that may influence the therapeutic response.[24] They identified gain-of-function 
NOTCH1 mutations (“N1”; these mutations mainly occur in the PEST region) in 19/574 cases of DLBCL. Among these cases, 95% were activated B-cell-like (ABC) diffuse large B-cell lymphoma and no other type of mutation (BCL6 fusions (B) NOTCH2 (N2), or SPEN mutations) co-occurred suggesting that NOTCH1 and NOTCH2 act through different pathogenetic pathways.[24] Moreover, within ABC DLBCL, patients with N1 mutation had worse progression-free survival and overall survival compared to patients with N2 mutation.[24] These data highlight that N1 and N2 mutations are genetically, phenotypically, and clinically different, suggesting the need to extend targeting Notch1 in these aggressive forms of B-cell malignancies.
Here we review some of the latest strategies to target Notch in hematological malignancies with emphasizing innovative approaches or experiences that translated pre-clinical observations into clinical trials (Figure 2).

Figure 2 Figure 2. The figure shows an overview of therapeutic targeting of Notch signaling.

Targeting Extracellular NOTCH1

Unlike Notch pathway activation in mutated T-ALL, CLL, MCL, the canonical activation of Notch signaling is mediated by ligand-mediated mechanisms.[25,26] Thus, given the role of Notch in several humans’ cancers, the development of therapeutic agents that interfere with ligand-receptor binding has seen a great impetus in the last years.[27]
A strategy that has been extensively explored is the development of antibodies (Abs) to block Notch ligand-receptor interaction. Several groups developed receptors-directed antibodies designed to antagonize NOTCH1, 2 and 3 by recognizing the NRR region of NOTCH to prevent the ADAM mediated metalloprotease cleavage.[28-30]
For example, Aste-Amezaga reported the identification of two classes of NOTCH1 inhibitory monoclonal (m) Ab derived from cell-based and solid phase screening of a phage display library.[31] The first class comprises Abs directed to the EGF-repeat region (WC613), and the second directed to the NRR NOTCH1 domain (WC75). Both classes of antibodies inhibited canonical Notch signaling in vitro by repressing Notch transcriptional targets such as Hes1 and DTX1 genes. As predicted by the analysis of the putative NOTCH1 binding site, WC75 also inhibited Notch activation in a ligand-independent fashion such as in cancers mutated models (T-ALL), and similar to a 
γ-secretase inhibitor, Compound E, induced a gene expression signature consistent with Notch1 abrogation. Consistently WC75 inhibited the proliferation of NOTCH1 mutated T-ALL cell lines such as DND41 and KOPT-K1.[31]
Similarly OMP-52M51, a mAb generated by immunizing mice with a fragment of human NOTCH1 protein comprising the LNR plus the HD domain, efficiently blocked canonical Notch signal and reduced Notch activation in a series of T-ALL bearing HD and PEST mutations in vitro and in two patient-derived xenograft leukemia models carrying a L1679P mutation and a PEST deletion respectively.[32] In addition, OMP-52M51 prevented Notch1 activation in MCL cell lines in vitro.[33] OMP-52M51 (Brontictuzumab) was subsequently tested in a phase I dose escalation trial (NCT01778439) in patients with previously treated CLL, MCL, T-ALL, or other hematologic malignancies with known 
NOTCH1 mutational status. Of the 24 patients enrolled in this study, only five carried a NOTCH1 mutation, and just one of them achieved stable disease as the best response after 101 days of treatment. Overall OMP-52M51 was generally well tolerated but showed limited antitumor efficacy in this study.[34]
However, Sharma and colleagues further extended targeting NRR domain and reported the identification of the first mAb that recognizes clinically relevant mutant receptors.[35] The mAb 604.17 exhibited higher binding to mutant NOTCH1 compared to wild type and inhibited the proliferation of the T-ALL mutated cell line CCRF-CEM. Interestingly, 2 µg/mL of mAb 604.17 preferentially inhibited the transcriptional activation of the NOTCH1 mutants L1549P, R1599P, and II1681N as assessed with a validated RPBJ 12xCSL-luciferase promoter assay. Finally, 15 mg/kg of mAb 604.17 inhibited the tumor growth of different xenograft cancer models supporting the development of Notch mAbs as immunotherapeutic tools for different cancers.[35]
Besides Abs directed to NOTCH1 NRR domain, additional probes have been developed to NOTCH2 and NOTCH3.[28] For example, OMP-59R5 (Tarextumab), was generated by panning the HuCAL GOLD phage-display library with recombinant NOTCH2 extracellular domain (EGF1–12) containing the ligand-binding site. OMP-59R5 showed antitumor activity in breast, ovarian, and small-cell lung cancer.[36] A phase Ib clinical trial showed that Tarextumab is well tolerated, and showed a dose-dependent biomarker-driven activity in patients with small-cell lung cancer (SCLC).[37,38]
The Blacklow laboratory leveraged the development of inhibitors and activators NRR mAbs to dissect the dynamics of NOTCH3 activation.[39,40] Given the prevalence of NOTCH3 activation (ICN3) and the recurrence of NOTCH3 mutations in different cancer models, including T-ALL, the authors demonstrated that MOR20350 and MOR20358 inhibited Notch3 signaling in vitro.[41,42] MOR20350 and MOR20358 exhibited an anti-tumor effect using orthotopic xenograft models representative of cancer carrying a NOTCH3 PEST (MDA-MB468) or NRR (TALL-1) mutations, respectively.[41]
A second strategy to inhibit Notch signaling is by developing Abs directed against Notch ligands such as DLL1 and DLL4.[43] For example, OMP-21M18 emerged from murine hybridoma library screen set to identify DLL4 inhibitors using a Notch-responsive luciferase reporter assay in HeLa cells.[44] DLL4 has a unique role in regulating vascular endothelial cell proliferation and differentiation. Suppression of DLL4-mediated Notch signaling increases nonproductive angiogenesis but efficiently inhibited tumor growth in several cancer models.[45] However chronic inhibition of dll4 showed to alter normal liver endothelial histology in mice, rats, and cynomolgus monkeys and promotes subcutaneous vascular neoplasms in rats.[46] Despite safety concerns, OMP-21M18/Demcizumab entered clinical development, and it has been investigated in a phase I dose escalation and expansion study in patients with previously treated solid tumors (RGN-124, NCT01189929).[47] However, given the lack of clinical responses assessing the role of OMP-21M18 in combination with paclitaxel plus gemcitabine in treatment-naïve patients with metastatic pancreatic cancer OncoMed Pharmaceuticals discontinued ongoing demcizumab trials. Similarly to demcizumab, enoticumab a humanized IgG1 anti-Dll4 was tested in a phase I trial in ovarian cancers and solid tumors.[48] Enoticumab was well tolerated (most of the patients experienced fatigue, headache, hypertension, and nausea) and response to treatment was confirmed in 2 out 53 patients (5%) treated at 3 mg/kg (one patient with papillary serous ovarian carcinoma, and one patient with non–small cell lung cancer) while 16 patients (36%) had a stable disease.48 Demcizumab, enoticumab trials are not extended to patients with hematological malignancies so far.

Targeting the γ-Secretase Complex

Because of its crucial role in Alzheimer's disease pathology, γ-secretase has been the target of many small molecules that were initially designed to reduce the generation of Aβ polypeptides in the amyloid plaques. Among other substrates, the γ-secretase complex proteolyzes the release of ICN1 and therefore represents a critical step in the canonical Notch signaling. Thus, inhibitors of the γ-secretase complex (GSIs) that target all NOTCH receptors were re-purposed in cancers where NOTCH1 mutations are common (T-ALL, CLL) and tumor dependency has been established in preclinical models. For example, in T-ALL, several studies showed that GSI treatment induces G0/G1 arrest along with rapid clearance of intracellular NOTCH1.[49-52]
De Angelo and collaborators completed the first GSI trial in T-ALL in six adults and two pediatric patients with leukemia (seven with T-ALL) treated in average for 56 days with MK-0752 a potent inhibitor developed by Merck & Co. In a T-ALL patient, with an activating NOTCH1 mutation, the response was transient.[53] Overall, MK-0752 was poorly tolerated. In fact, most of the patients suffered from gastrointestinal toxicity, primarily diarrhea, observed at drug doses of 300 mg/m2. Subsequent studies showed that the gastrointestinal toxicity was due to the simultaneous blockade of NOTCH1 and NOTCH2 mediated by GSIs. Abrogation of the Notch1/2 signaling in the gut leads to severe intestinal secretory metaplasia, an increase of goblet cells and a differentiation failure in the crypts of the small intestine[54] suggesting that targeted inhibition of individual receptors might reduce on-target gut toxicity.[28]
The MK-0752 failure, rushed for the identification of second generations GSIs with better tolerability profile and of combination strategies to overcome the limitation showed with the single drug treatment. Real and colleagues demonstrated that glucocorticoid therapy in combination with NOTCH1 inhibition by GSIs improved the antileukemic effect of GSIs and reduced their gut toxicity in vivo.[55,56] GSI sensitizes steroids resistant T-ALL cell lines and primary patients to glucocorticoid therapy and induced apoptosis through induction of BCL2L11. Mice treated with glucocorticoids and a GSI showed decreased gastrointestinal toxicity compared to animals treated with GSI alone. Steroids mediate the induction of cyclin D2 (CCND2), a cyclin associated with cell cycle progression, and by the down-regulation of Kruppel-Like Factor 4 (KLF4), a negative regulator of the cell cycle that is required for goblet cell differentiation.[14,55] In addition, Cullion and collaborators demonstrated that intermittent GSI dosing with drug holiday largely avoided gastrointestinal toxicity while maintaining efficacy in a mouse T-ALL model.[57,58]
However, gut toxicity is not the only off-target effect seen in GSI treated patients, raising additional concerns on chronic inhibition of wild-type NOTCH1. In two early-terminated phase III trials, LY450139 (semagacestat), failed to achieve the primary endpoints (improvement in the cognition and the ability to complete activities of daily living) in patients with mild-to-moderate Alzheimer's disease.[59] Data showed that semagacestat was associated with an increased risk of skin cancer compared with those who received placebo, likely due to inhibition of Notch in the skin by chronic GSI administration consistent with the tumor-suppressor role of Notch signaling in this tissue.[60,61] In addition, recent studies suggested that Notch signaling blockade might increase the risk of developing lung squamous cell carcinoma (SCC).[62] Whether this risk will be ameliorated by intermittent, pulsed therapy with GSI, as would be the schedule in cancer-directed therapy, is still to be determined.[14]
An additional GSI that reached clinical development is PF-03084014/Nirogacestat a noncompetitive, reversible GSI developed by Pfizer.[63] PF-03084014 induced an anti-leukemic effect in vitro and in vivo in T-ALL cell lines expressing mutant NOTCH1. An intermittent dosing schedule of PF-03084014 and the addition of glucocorticoids attenuated Notch-dependent gastrointestinal toxicity by reducing the loss of body weight in an HBP-ALL T-ALL xenograft model[63] confirming previous Cullion’s observations. PF-03084014 induces selective apoptosis in primary CLL cells carrying 
NOTCH1 mutations and synergize with fludarabine in a stroma coculture model system.[64] In a phase I trial aimed to determine the safety profile and maximum tolerated dose (MTD) of PF-03084014, one out of eight relapsed/refractory T-ALL patients achieved a complete remission.[65]
Knoechel and colleagues reported a complete hematological response in a patient with early T-cell precursor acute lymphoblastic leukemia (ETP-ALL) carrying a 
NOTCH1 mutation treated with the GSI developed by the Bristol-Myers-Squibb 906024. A phase I trial, CA216002, confirmed this encouraging result and demonstrated the safety of BMS-906024 administered on weekly dosing (4-6 mg) in 25 pediatric patients with T-ALL or T-cell lymphoblastic lymphoma.[66] This study was the first trial reporting multiple responses to GSI inhibition, including a complete response and one partial response. Overall, 32% of the patients showed at least a 50% reduction in bone marrow (BM) blasts with tolerable side effects.[66] Interestingly, in pre-clinical studies, BMS-906024 enhanced the anti-leukemic activity of Ibrutinib in B-CLL cells in vitro by inhibiting ICN1 activation and consequently the transcription of its targets such as c-MYC.[67]
An alternative strategy to modulate 
γ-secretase activity is by developing mAbs directed to functional components of this complex. The γ-secretase complex comprises a catalytic core formed by presenilin 1 and presenilin 2 (PS1 and PS2) and three accessory proteins: anterior pharynx-defective 1 (APH-1), nicastrin (NCT), and presenilin enhancer protein 2 (PEN2).[68] For example, Hayashi and colleagues reported the identification of two mAbs A5226A and A5201A directed against the extracellular domain of NCT.[69,70] A5226A inhibited γ-secretase activity by competing with the NCT substrate binding in vitro. In addition, A5226A inhibited the proliferation of a NOTCH1 mutated T-ALL cell line, DND41, and prevented ICN1 cleavage. In a xenograft model of DND41, A5226A administered at 50 mg/Kg/day reduced cancer cells growth in vivo.[69]
As discussed above, several GSIs showed preclinical activity and have entered late development,[71] limitations include lack of substrate selectivity and toxicities.[72] In addition, genetic and epigenetic mechanisms of resistance partially explained the lack of successful clinical translation on a large scale. To identify mechanisms of resistance to NOTCH1 inhibition in T-ALL, the laboratory of Dr. Ferrando analyzed the global gene expression signatures associated with a sensitivity of resistance to GSI. They demonstrated that the transcriptional suppression of PTEN was associated with resistance to GSI treatment in T-ALL cell lines. Protein analysis and mutation sequencing showed the absence, or the marked reduction of PTEN at the protein level and biallelic PTEN mutation in resistant T-ALL cell lines.[73,74]
Knoechel and collaborators described an additional mechanism of tolerance to GSI therapy. In this work, the authors identified from in vitro long-term culture under GSI positive selections a subpopulation of GSI-tolerant T-ALL cells called “persister”. They described that resistance to GSI was reversible after the drug’s withdrawal; thus, they speculated the existence of an epigenetic mechanism of drug resistance. Therefore, they performed a short hairpin RNA (shRNA) screen targeting genes involved in chromatin regulation. Among top hits, which preferentially impaired the viability of “persister” cells while sparing the naïve population, they identified the BET (bromodomain and extra-terminal domain) family, BRD4. Consistently “persister” cells were more sensitive to BRD4 inhibition (JQ1) in vitro and combination therapy targeting “naïve” (GSI) and “persister” (JQ1) was significantly more effective in T-ALL xenotransplant models in vivo.[75]

Targeting NOTCH Trafficking

As we described above, NOTCH1 is a rational therapeutic target in several hematological malignancies, but as a mutated transcription factor, it poses a drug discovery challenge. Several groups contributed to the development of a program to overcome limitations associated with the targeting of transcription factors (e.g. NOTCH1)[76-81] or resistance to target therapy.[82-84] For example, we completed a gene expression-based high-throughput small molecule (GE-HTS)[49,85] and a cDNA overexpression screen using cell-based assays reporting Notch transcriptional activity.[86] To enrich for targets that preferentially impair NOTCH1 receptor bearing HD mutations (NRR), we deliberately selected to screen against a human T-ALL cell line (DND41), which carries a clinically relevant activating mutation in the HD of NOTCH1 along with a PEST domain deletion (L1594PΔPEST) and secondly to identify gene products that would enhance the activation of a transcriptional reporter downstream of a mutant NOTCH1 receptor frequently identified in T-ALL patients (L1601PΔPEST). Several ion flux modulators or genes encoding for ion channels or pumps scored as hits in the small molecules or the cDNA screens, respectively. One of the top compound hits was thapsigargicin, an analog of thapsigargin, which is a non competitive inhibitor of the sarco/endoplasmic reticulum Ca2+-ATPase (SERCA). Among the top cDNA hits were ATP2A1, ATP2A2, and ATP2A3, which encode SERCA1, SERCA2, and SERCA3, respectively. We next showed that SERCA inhibition impairs the trafficking of mutated NOTCH1 receptors and induces a G0/G1 arrest in NOTCH1-mutated human T-ALL cells (Figure 1B). Thapsigargin had on-target activity in mouse models of human T-ALL and also interfered with Notch signaling in Drosophila.[76,87] Remarkably, thapsigargin preferentially inhibited mutated NOTCH1 receptors.[76] This selectivity provides a therapeutic window not observed before with GSIs or most antibody-based approaches that are equipotent inhibitors of mutated and wild type (WT) receptors. Subsequent independent studies confirmed our original observation and demonstrated that thapsigargin alone or in combination with mAb 604.107 inhibited “gain of function” mutants associated with T-ALL such as L1594P, R1599P and I168N.[35]
Thapsigargin is an organic heterotricyclic compound that is a hexa-
γoxygenated 6,7-guaianolide isolated from the roots of Thapsia garganica. Thapsigargin inhibits SERCA-mediated calcium (Ca2+) uptake leading to a depletion of the endoplasmic reticulum (ER) Ca2+ storage and sustained elevation of cytosolic Ca2+ triggering ER stress, [76] unfolded protein response (UPR), and different cellular pathways that can cause cell death. This general mechanism of cytotoxicity to develop SERCA inhibitors for cancer therapies has been leveraged . For example, SERCA has been identified as an emerging target in the treatment of prostate cancer.[88] SERCA channels are critical to maintaining intracellular Ca2+ homeostasis in all cell types. Thus, the direct delivery of thapsigargin to animals or humans might be expected to incur cardiac toxicity secondary to Ca2+ ion shifts. A strategy to prevent a systemic cytotoxic effect by inhibiting SERCA is by creating inactive pro-drugs that are activated in a histo-specific manner.[89] This, for example, is the mode of action of mipsagargin,[90,91] a TG soluble prodrug undergoing clinical trials for solid tumor.[89]
In the past, we imagined a general strategy for efficient TG delivery leveraging the dependency to folate metabolism of leukemia cells and developed a folate-TG derivative compound to transfer the inhibitor specifically to the T-ALL cells.[92] We showed that the 8-O-debutanoylthapsigargin, a cytotoxic TG analog, retained the anti-leukemia specificity toward mutant NOTCH1 in T-ALL cell lines. Thus, we linked the carboxylate of folic acid to the C8-alcohol of 8-O-debutanoylthapsigargin, to generate the folate-thapsigargin conjugate named JQ-FT. We demonstrated that JQ-FT inhibits NOTCH1 in vitro in multiple T-ALL models and in vivo on a syngeneic T-ALL mouse model carrying a 
NOTCH1 L1601P ΔPEST a common mutation observed in the human disease.[92] In the Notch arena, JQ-FT is the first-in-class NOTCH1 inhibitor with dual selectivity: leukemia over normal and NOTCH1-mutant over wild type receptors.
In the recent past, several putative SERCA inhibitors have been described. However, only a few have been tested in Notch-dependent diseases. Ford and colleagues demonstrated that the natural tricyclic clerodane diterpene casearin J (CJ),[93] can affect the Notch1 pathway in human T-ALL cells. CJ reduced cell surface expression of NOTCH1 receptors, prevented the formation of the cleaved ICN1 molecules, which resulted in the transcriptional inhibition of Notch targets such as MYC, HES1. The authors showed that CJ inhibits SERCA protein causing a rise of intracellular Ca
2+ and depletion of the ER Ca2+ storage. This ion shift concentration increases reactive oxygen species (ROS) and ultimately leads to apoptosis in T-ALL cells.[93] However, while the authors claimed selectivity toward HD-mutations, they did not demonstrate the lack of CJ activity in a large panel of wild type T-ALL models. In addition, is not clear whether CJ causes an accumulation of full-length NOTCH1, as for other SERCA inhibitors,[76] suggesting that different interactions in the SERCA binding site may be responsible for the effect on Ca2+ and consequently on Notch activation.
Ethyl 2-Amino-6-(3,5-dimethoxyphenyl)-4-(2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate  (CXL017) is a recently synthesized SERCA inhibitor tested in multiple leukemia cell lines that acquired multidrug resistance through different mechanisms, including T-ALL.[94] Additional studies demonstrated that CXL017 synergizes with other SERCA inhibitors including thapsigargin and cyclopiazonic acid indicating that CXL017 may bind SERCA at a unique allosteric site[95] pointing to the potential of developing new classes of SERCA modulators.
In our original GE-HTS screen, multiple compounds reported modulating Ca
2+ ion flux scored as dose-dependent Notch pathway inhibitors including ionomycin, salinomycin, and bepridil.[76] Thus we initially extended testing the FDA approved Ca2+ antagonist bepridil in T-ALL.[96] In vitro, bepridil reduced ICN1 and consequently caused a phenotype consistent with Notch abrogation in this tumor. While we can reach this effect at the plasma level concentration achievable in human, we did not demonstrate an effect in T-ALL orthographs, and we halted further experiments.[96] However, because we showed a transcriptional overlap between the NOTCH1Off” signatures in T-ALL and CLL, we re-purposed bepridil for B-cell malignancies.[97] In CLL bepridil exerted an anti-leukemia activity in vivo associated with NOTCH1 inhibition.[97] Similar to thapsigargin, histological analysis of the gut showed normal goblet cell number with preservation of the architecture and proliferation of the intestinal epithelium suggesting a lack of combined NOTCH1 and NOTCH2 inhibition in this tissue. This result suggests Ca2+ mediated inhibition of Notch signaling may overcome the limitation associated with γ-secretase inhibition.
An additional strategy to alter NOTCH trafficking is by modulating the protein O-fucosyltransferase-1. POFUT1 catalyzes the addition of O-linked fucose to the EGF-repeat domains of the NOTCH receptor that is required for NOTCH activation.[98] McMillan and colleagues showed that CRISPR/Cas9 mediated POFUT1 knockout in U2OS cells suppresses Notch activation signaling associated with type I and II mutations.[99] Interestingly, NOTCH1 protein does not mature in the CRISPR-engineered U2OS cells lacking POFUT1, a phenotype that mimics closely TG inhibition.

Targeting NOTCH Degradation

NOTCH is a short-lived protein and undergoes degradation mainly through an E3-ligase (Fbw7) ubiquitin-mediated pathway controlled by the PEST domain. As we described above, disruption of the PEST domain leads to an increase in ICN half-life.[25] In recent work, Koyama and colleagues demonstrated that the proteasome inhibitor, bortezomib, repressed the transcription of NOTCH1 and of its downstream targets including HES1, GATA3, RUNX3 and CYLD in MOLT4, JURKAT and CEM T-ALL cell lines.[100]
Drug combination studies revealed that bortezomib showed synergistic or additive effects with key drugs to treat T-ALL such as dexamethasone, doxorubicin, and cyclophosphamide. The synergistic effect of bortezomib and dexamethasone was confirmed at NOTCH1 protein expression level and later in vivo using a murine MOLT-4 T-ALL cell xenograft model.[100] This study supported the rationale of an ongoing clinical trial assessing the role of bortezomib in combination with different chemotherapy regimen (NCT02112916) in younger patients with newly diagnosed T-ALL or stage II-IV T-cell lymphoblastic lymphoma.
In parallel, Bertaina and colleagues tested bortezomib in combination with chemotherapy in 30 and 7 children with B-cell precursor (BCP) and T-cell ALL, respectively.[101] Bortezomib (1.3 mg/m2/dose) was administered intravenously twice a week x 2 with a chemotherapy regimen containing dexamethasone, doxorubicin, vincristine, and pegylated asparaginase. Twenty-two of 30 BCP-ALL patients (73,3%) and 5/7 patients (71%) with T-cell ALL achieved CR/CRp. The 2-year overall survival (OS) was 31,3% while patients that achieved an MRD response had a 2-year OS of 68·4%.[101] These data suggest that bortezomib may represent a clinically effective option in 
NOTCH1 mutated T-ALL patients.
In CLL, Notch2 signaling appears to have a constitutive role in promoting cell survival and CD23 expression.[102,103] Several studies showed that B-CLL undergoes apoptosis upon proteasome inhibitors treatment.[104,105] However, Duecheler and colleagues demonstrated that bortezomib and MG132 efficiently induced apoptosis in B-CLLs in vitro by inhibiting NOTCH2 transactivation and repressing CD23 expression.[106] Similarly, in MCL, several studies demonstrated the effects of proteasome inhibition on several intracellular mechanisms.[107] For example, bortezomib showed to induce cell cycle arrest and apoptosis by inhibition of NF-kB,[108] inhibition of the protein kinase CK2,[109,110] the depolarization of the mitochondria membrane, ROS release, and the production of pro-apoptotic proteins (NOXA).[111] In addition, several pre-clinical studies demonstrated the synergist activity of bortezomib with other antineoplastic agents[112,113] including the HDAC inhibitor vorinostat (SAHA),[114] idelalisib,[
115] and the anti-CD20 mAb rituximab.[116] While many clinical trials confirmed that combining bortezomib with other anti-lymphoma therapies is feasible effective none at the moment focused on the role of Notch signaling mediating the efficacy or resistant to therapy.

Targeting ICN1 Complex

As described above, activation of NOTCH1 receptor results in a sequence of cleavages that cause the release of ICN1. Following translocation to the nucleus, ICN1 forms a ternary complex with the transcriptional repressor CSL (CBF-1, Suppressor of Hairless and Lag-1) co-activators of the Mastermind-like family (MAML1-3 in humans) bound to DNA. Thus, Moellering and colleagues developed a cellular penetrant, soluble α-Helix-constrained “stapled” peptide derived from mastermind-like 1, SAHM1 that can bind the ICN-CSL complex. Similarly to GSI, SAHM1 produced a transcriptional signature of NOTCH gene repression in human and murine T-ALL cells. Direct blockade of NOTCH-CSL transcriptional complex reduced NOTCH-specific anti- proliferative effects in human T-ALL cell lines and in a bioluminescent murine model of T-ALL.[117]
While this approach holds the premises to be more specific for Notch compared to GSIs, which also affect the cleavage of different cellular substrates, its clinical translation is hampered by the lack of pharmacokinetics and pharmacodynamics studies.
Recently Cellestia Biotech AG developed CB-103 a small molecule protein-protein interaction (PPI) inhibitor able to target assembly of the Notch transcription complex in the cell nucleus leading to down-regulation of Notch target genes (c-MYC, CCND1, HES1) and inhibition of Notch signaling independently of Notch mechanisms of activation. This pan-Notch inhibitor has shown preclinical activity in a variety of solid tumors and leukemia models. In preclinical studies CB-103 inhibited the proliferation of various cancer cell lines including T-ALL with known 
NOTCH1 mutational status (RPMI-8402 and KOPT-K1) compared to the GSI 4929097. Both ICN1, transmembrane NOTCH1 and full-length decrease upon CB-103 treatment consistent with a mechanism of transcriptional inhibition.[118] Spriano and colleagues extended testing CB-103 in a collection of 61 B and T cell lymphoma cell lines. CB-103 presented a median IC50 above 20 µM across the whole panel of lymphoma cell lines (range from 400 nM to > 20 µM), without significant differences among lymphoma subtypes.[119] Sensitive lines (IC50 < 10 µM) presented a gene expression signature significantly enriched with genes involved in the epithelial-mesenchymal transition, a Notch-related process.[119] A multicenter open-label, non randomised phase I-II clinical trial (CB-103-C-101) is ongoing, enrolling patients with advanced, refractory or metastatic solid tumors and hematological malignancies for whom no standard therapy exists.[120] Notch mutational status or expression is not key inclusion criteria of the study but it stands among the exploratory analysis suggesting that, as in other previous studies, responses in Notch mutated cases may be few.


In the last two decades, we have seen significant improvements in T-ALL, CLL and MCL survival. However, a significant number of patients relapse or rapidly became resistant to available therapeutic options. Thus, the development of a Notch targeted approach appears a rational strategy to modulate a pathway on which these cancer cells rely on to survive. Despite γ-secretase inhibitors experienced several roadblocks in their development we are achieving a better characterization of disease's pathways that will facilitate the development of mutant selective of context-dependent inhibitors for these aggressive tumors. Furthermore, the development of Notch isoform selective small molecules along with re-defined therapeutic schedule will overcome the hurdle associated with the off-target toxicities seen with the chronic inhibition of wild type NOTCH1 and NOTCH2.


This work was supported by an AIRC Start-up Investigator Grant (n. 17107 G.R.), Fondazione Cariparma (3576/2017, 0180/2018 G.R.), Fondazione Grande Ale Onlus (G.R.), Fondazione Umberto Veronesi Post-doctoral Fellowship (C.S.).


  1. Lawrence MS, Stojanov P, Mermel CH, Robinson JT, Garraway LA, Golub TR, Meyerson M, Gabriel SB, Lander ES, Getz G. Discovery and saturation analysis of cancer genes across 21 tumour types. Nature. 2014;505(7484):495-501. PMid:24390350 PMCid:PMC4048962
  2. Artavanis-Tsakonas S, Rand MD, Lake RJ. Notch signaling: cell fate control and signal integration in development. Science. 1999;284(5415):770-776. PMid:10221902
  3. Kopan R, Ilagan MX. The canonical Notch signaling pathway: unfolding the activation mechanism. Cell. 2009;137(2):216-233. PMid:19379690 PMCid:PMC2827930
  4. Gordon WR, Roy M, Vardar-Ulu D, Garfinkel M, Mansour MR, Aster JC, Blacklow SC. Structure of the Notch1-negative regulatory region: implications for normal activation and pathogenic signaling in T-ALL. Blood. 2009;113(18):4381-4390. PMid:19075186 PMCid:PMC2676092
  5. Gordon WR, Vardar-Ulu D, Histen G, Sanchez-Irizarry C, Aster JC, Blacklow SC. Structural basis for autoinhibition of Notch. Nat Struct Mol Biol. 2007;14(4):295-300. PMid:17401372
  6. Brou C, Logeat F, Gupta N, Bessia C, LeBail O, Doedens JR, Cumano A, Roux P, Black RA, Israel A. A novel proteolytic cleavage involved in Notch signaling: the role of the disintegrin-metalloprotease TACE. Mol Cell. 2000;5(2):207-216.
  7. Moretti J, Brou C. Ubiquitinations in the notch signaling pathway. Int J Mol Sci. 2013;14(3):6359-6381. PMid:23519106 PMCid:PMC3634445
  8. Sanchez-Irizarry C, Carpenter AC, Weng AP, Pear WS, Aster JC, Blacklow SC. Notch subunit heterodimerization and prevention of ligand-independent proteolytic activation depend, respectively, on a novel domain and the LNR repeats. Mol Cell Biol. 2004;24(21):9265-9273. PMid:15485896 PMCid:PMC522238
  9. De Strooper B, Annaert W, Cupers P, Saftig P, Craessaerts K, Mumm JS, Schroeter EH, Schrijvers V, Wolfe MS, Ray WJ, Goate A, Kopan R. A presenilin-1-dependent gamma- secretase-like protease mediates release of Notch intracellular domain. Nature. 1999;398(6727):518-522. PMid:10206645
  10. Ellisen LW, Bird J, West DC, Soreng AL, Reynolds TC, Smith SD, Sklar J. TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms. Cell. 1991;66(4):649-661.
  11. Ferrando AA. The role of NOTCH1 signaling in T-ALL. Hematology Am Soc Hematol Educ Program. 2009:353-361. PMid:20008221 PMCid:PMC2847371
  12. Weng AP, Ferrando AA, Lee W, Morris JP, Silverman LB, Sanchez-Irizarry C, Blacklow SC, Look AT, Aster JC. Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia. Science. 2004;306(5694):269-271. PMid:15472075
  13. Malecki MJ, Sanchez-Irizarry C, Mitchell JL, Histen G, Xu ML, Aster JC, Blacklow SC. Leukemia-associated mutations within the NOTCH1 heterodimerization domain fall into at least two distinct mechanistic classes. Mol Cell Biol. 2006;26(12):4642-4651. PMid:16738328 PMCid:PMC1489116
  14. Roti G, Stegmaier K. Targeting NOTCH1 in hematopoietic malignancy. Crit Rev Oncog. 2011;16(1-2):103-115.
  15. Di Ianni M, Baldoni S, Rosati E, Ciurnelli R, Cavalli L, Martelli MF, Marconi P, Screpanti I, Falzetti F. A new genetic lesion in B-CLL: a NOTCH1 PEST domain mutation. Br J Haematol. 2009;146(6):689-691. PMid:19604236
  16. Puente XS, Pinyol M, Quesada V, Conde L, Ordonez GR, Villamor N, Escaramis G, Jares P, Bea S, Gonzalez-Diaz M, Bassaganyas L, Baumann T, Juan M, Lopez-Guerra M, Colomer D, Tubio JM, Lopez C, Navarro A, Tornador C, Aymerich M, Rozman M, Hernandez JM, Puente DA, Freije JM, Velasco G, Gutierrez-Fernandez A, Costa D, Carrio A, Guijarro S, Enjuanes A, Hernandez L, Yague J, Nicolas P, Romeo-Casabona CM, Himmelbauer H, Castillo E, Dohm JC, de Sanjose S, Piris MA, de Alava E, San Miguel J, Royo R, Gelpi JL, Torrents D, Orozco M, Pisano DG, Valencia A, Guigo R, Bayes M, Heath S, Gut M, Klatt P, Marshall J, Raine K, Stebbings LA, Futreal PA, Stratton MR, Campbell PJ, Gut I, Lopez-Guillermo A, Estivill X, Montserrat E, Lopez-Otin C, Campo E. Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature. 2011;475(7354):101-105. PMid:21642962 PMCid:PMC3322590
  17. Arruga F, Gizdic B, Serra S, Vaisitti T, Ciardullo C, Coscia M, Laurenti L, D'Arena G, Jaksic O, Inghirami G, Rossi D, Gaidano G, Deaglio S. Functional impact of NOTCH1 mutations in chronic lymphocytic leukemia. Leukemia. 2014;28(5):1060-1070. PMid:24170027
  18. Kridel R, Meissner B, Rogic S, Boyle M, Telenius A, Woolcock B, Gunawardana J, Jenkins C, Cochrane C, Ben-Neriah S, Tan K, Morin RD, Opat S, Sehn LH, Connors JM, Marra MA, Weng AP, Steidl C, Gascoyne RD. Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. Blood. 2012;119(9):1963-1971. PMid:22210878
  19. Bea S, Valdes-Mas R, Navarro A, Salaverria I, Martin-Garcia D, Jares P, Gine E, Pinyol M, Royo C, Nadeu F, Conde L, Juan M, Clot G, Vizan P, Di Croce L, Puente DA, Lopez- Guerra M, Moros A, Roue G, Aymerich M, Villamor N, Colomo L, Martinez A, Valera A, Martin-Subero JI, Amador V, Hernandez L, Rozman M, Enjuanes A, Forcada P, Muntanola A, Hartmann EM, Calasanz MJ, Rosenwald A, Ott G, Hernandez-Rivas JM, Klapper W, Siebert R, Wiestner A, Wilson WH, Colomer D, Lopez-Guillermo A, Lopez- Otin C, Puente XS, Campo E. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma. Proc Natl Acad Sci U S A. 2013;110(45):18250-18255. PMid:24145436 PMCid:PMC3831489
  20. Fabbri G, Holmes AB, Viganotti M, Scuoppo C, Belver L, Herranz D, Yan XJ, Kieso Y, Rossi D, Gaidano G, Chiorazzi N, Ferrando AA, Dalla-Favera R. Common nonmutational NOTCH1 activation in chronic lymphocytic leukemia. Proc Natl Acad Sci U S A. 2017;114(14):E2911-E2919. PMid:28314854 PMCid:PMC5389283
  21. Baliakas P, Hadzidimitriou A, Sutton LA, Rossi D, Minga E, Villamor N, Larrayoz M, Kminkova J, Agathangelidis A, Davis Z, Tausch E, Stalika E, Kantorova B, Mansouri L, Scarfo L, Cortese D, Navrkalova V, Rose-Zerilli MJ, Smedby KE, Juliusson G, Anagnostopoulos A, Makris AM, Navarro A, Delgado J, Oscier D, Belessi C, Stilgenbauer S, Ghia P, Pospisilova S, Gaidano G, Campo E, Strefford JC, Stamatopoulos K, Rosenquist R, European Research Initiative on CLL. Recurrent mutations refine prognosis in chronic lymphocytic leukemia. Leukemia. 2015;29(2):329-336. PMid:24943832
  22. Inamdar AA, Goy A, Ayoub NM, Attia C, Oton L, Taruvai V, Costales M, Lin YT, Pecora A, Suh KS. Mantle cell lymphoma in the era of precision medicine-diagnosis, biomarkers and therapeutic agents. Oncotarget. 2016;7(30):48692-48731. PMid:27119356 PMCid:PMC5217048
  23. Rossi D, Rasi S, Fabbri G, Spina V, Fangazio M, Forconi F, Marasca R, Laurenti L, Bruscaggin A, Cerri M, Monti S, Cresta S, Fama R, De Paoli L, Bulian P, Gattei V, Guarini A, Deaglio S, Capello D, Rabadan R, Pasqualucci L, Dalla-Favera R, Foa R, Gaidano G. Mutations of NOTCH1 are an independent predictor of survival in chronic lymphocytic leukemia. Blood. 2012;119(2):521-529. PMid:22077063 PMCid:PMC3257017
  24. Schmitz R, Wright GW, Huang DW, Johnson CA, Phelan JD, Wang JQ, Roulland S, Kasbekar M, Young RM, Shaffer AL, Hodson DJ, Xiao W, Yu X, Yang Y, Zhao H, Xu W, Liu X, Zhou B, Du W, Chan WC, Jaffe ES, Gascoyne RD, Connors JM, Campo E, Lopez-Guillermo A, Rosenwald A, Ott G, Delabie J, Rimsza LM, Tay Kuang Wei K, Zelenetz AD, Leonard JP, Bartlett NL, Tran B, Shetty J, Zhao Y, Soppet DR, Pittaluga S, Wilson WH, Staudt LM. Genetics and Pathogenesis of Diffuse Large B-Cell Lymphoma. N Engl J Med. 2018;378(15):1396-1407. PMid:29641966 PMCid:PMC6010183
  25. Chiang MY, Radojcic V, Maillard I. Oncogenic Notch signaling in T-cell and B-cell lymphoproliferative disorders. Curr Opin Hematol. 2016;23(4):362-370. PMid:27135981 PMCid:PMC4962559
  26. Gu Y, Masiero M, Banham AH. Notch signaling: its roles and therapeutic potential in hematological malignancies. Oncotarget. 2016;7(20):29804-29823. PMid:26934331 PMCid:PMC5045435
  27. Cuesta-Mateos C, Alcaraz-Serna A, Somovilla-Crespo B, Munoz-Calleja C. Monoclonal Antibody Therapies for Hematological Malignancies: Not Just Lineage-Specific Targets. Front Immunol. 2017;8:1936. PMid:29387053 PMCid:PMC5776327
  28. Wu Y, Cain-Hom C, Choy L, Hagenbeek TJ, de Leon GP, Chen Y, Finkle D, Venook R, Wu X, Ridgway J, Schahin-Reed D, Dow GJ, Shelton A, Stawicki S, Watts RJ, Zhang J, Choy R, Howard P, Kadyk L, Yan M, Zha J, Callahan CA, Hymowitz SG, Siebel CW. Therapeutic antibody targeting of individual Notch receptors. Nature. 2010;464(7291):1052-1057. PMid:20393564
  29. Yuan X, Wu H, Xu H, Xiong H, Chu Q, Yu S, Wu GS, Wu K. Notch signaling: an emerging therapeutic target for cancer treatment. Cancer Lett. 2015;369(1):20-27. PMid:26341688
  30. Bellavia D, Palermo R, Felli MP, Screpanti I, Checquolo S. Notch signaling as a therapeutic target for acute lymphoblastic leukemia. Expert Opin Ther Targets. 2018;22(4):331-342. PMid:29527929
  31. Aste-Amezaga M, Zhang N, Lineberger JE, Arnold BA, Toner TJ, Gu M, Huang L, Vitelli S, Vo KT, Haytko P, Zhao JZ, Baleydier F, L'Heureux S, Wang H, Gordon WR, Thoryk E, Andrawes MB, Tiyanont K, Stegmaier K, Roti G, Ross KN, Franlin LL, Wang H, Wang F, Chastain M, Bett AJ, Audoly LP, Aster JC, Blacklow SC, Huber HE. Characterization of Notch1 antibodies that inhibit signaling of both normal and mutated Notch1 receptors. PLoS One. 2010;5(2):e9094. PMid:20161710 PMCid:PMC2817004
  32. Agnusdei V, Minuzzo S, Frasson C, Grassi A, Axelrod F, Satyal S, Gurney A, Hoey T, Seganfreddo E, Basso G, Valtorta S, Moresco RM, Amadori A, Indraccolo S. Therapeutic antibody targeting of Notch1 in T-acute lymphoblastic leukemia xenografts. Leukemia. 2014;28(2):278-288. PMid:23774673
  33. Höring E, Colom Sanmarti B, Xargay-Torrent S, Aulitzky WE, van der Kuip H, Campo E, López-Guerra M, Colomer D. Notch1 Signaling in <em>NOTCH1</em>-Mutated Mantle Cell Lymphoma Depends on DLL4 and Is a Potential Target for Specific Antibody Therapy. Blood. 2016;128:1846-1846.
  34. Casulo C, Ruan J, Dang NH, Gore L, Diefenbach C, Beaven AW, Castro JE, Porcu P, Faoro L, Dupont J, Kapoun A, Wang M, McGuire K, Flinn IW. Safety and Preliminary Efficacy Results of a Phase I First-in-Human Study of the Novel Notch-1 Targeting Antibody Brontictuzumab (OMP-52M51) Administered Intravenously to Patients with Hematologic Malignancies. Blood. 2016;128:5108-5108.
  35. Sharma A, Gadkari RA, Ramakanth SV, Padmanabhan K, Madhumathi DS, Devi L, Appaji L, Aster JC, Rangarajan A, Dighe RR. A novel Monoclonal Antibody against Notch1 Targets Leukemia-associated Mutant Notch1 and Depletes Therapy Resistant Cancer Stem Cells in Solid Tumors. Sci Rep. 2015;5:11012. PMid:26046801 PMCid:PMC4457015
  36. Yen WC, Fischer MM, Axelrod F, Bond C, Cain J, Cancilla B, Henner WR, Meisner R, Sato A, Shah J, Tang T, Wallace B, Wang M, Zhang C, Kapoun AM, Lewicki J, Gurney A, Hoey T. Targeting Notch signaling with a Notch2/Notch3 antagonist (tarextumab) inhibits tumor growth and decreases tumor-initiating cell frequency. Clin Cancer Res. 2015;21(9):2084-2095. PMid:25934888
  37. MC P. Final results of phase Ib of tarextumab (TRXT, OMP-59R5, anti-Notch2/3) in combination with etoposide and platinum (EP) in patients (pts) with untreated extensive- stage small-cell lung cancer (ED-SCLC). J Clin Oncol. 2015;33:abstr 7508.
  38. Smith DC, Chugh R, Patnaik A, Papadopoulos KP, Wang M, Kapoun AM, Xu L, Dupont J, Stagg RJ, Tolcher A. A phase 1 dose escalation and expansion study of Tarextumab (OMP-59R5) in patients with solid tumors. Invest New Drugs. 2018. PMCid:PMC6440937
  39. Tiyanont K, Wales TE, Siebel CW, Engen JR, Blacklow SC. Insights into Notch3 activation and inhibition mediated by antibodies directed against its negative regulatory region. J Mol Biol. 2013;425(17):3192-3204. PMid:23747483 PMCid:PMC3751422
  40. Xu X, Choi SH, Hu T, Tiyanont K, Habets R, Groot AJ, Vooijs M, Aster JC, Chopra R, Fryer C, Blacklow SC. Insights into Autoregulation of Notch3 from Structural and Functional Studies of Its Negative Regulatory Region. Structure. 2015;23(7):1227-1235. PMid:26051713 PMCid:PMC4497832
  41. Bernasconi-Elias P, Hu T, Jenkins D, Firestone B, Gans S, Kurth E, Capodieci P, Deplazes- Lauber J, Petropoulos K, Thiel P, Ponsel D, Hee Choi S, LeMotte P, London A, Goetcshkes M, Nolin E, Jones MD, Slocum K, Kluk MJ, Weinstock DM, Christodoulou A, Weinberg O, Jaehrling J, Ettenberg SA, Buckler A, Blacklow SC, Aster JC, Fryer CJ. Characterization of activating mutations of NOTCH3 in T-cell acute lymphoblastic leukemia and anti-leukemic activity of NOTCH3 inhibitory antibodies. Oncogene. 2016;35(47):6077-6086. PMid:27157619 PMCid:PMC5102827
  42. Choi SH, Severson E, Pear WS, Liu XS, Aster JC, Blacklow SC. The common oncogenomic program of NOTCH1 and NOTCH3 signaling in T-cell acute lymphoblastic leukemia. PLoS One. 2017;12(10):e0185762. PMid:29023469 PMCid:PMC5638296
  43. Briot A, Iruela-Arispe ML. Blockade of specific NOTCH ligands: a new promising approach in cancer therapy. Cancer Discov. 2015;5(2):112-114. PMid:25656896 PMCid:PMC4342039
  44. Hoey T, Yen WC, Axelrod F, Basi J, Donigian L, Dylla S, Fitch-Bruhns M, Lazetic S, Park IK, Sato A, Satyal S, Wang X, Clarke MF, Lewicki J, Gurney A. DLL4 blockade inhibits tumor growth and reduces tumor-initiating cell frequency. Cell stem cell. 2009;5(2):168- 177. PMid:19664991
  45. Ridgway J, Zhang G, Wu Y, Stawicki S, Liang WC, Chanthery Y, Kowalski J, Watts RJ, Callahan C, Kasman I, Singh M, Chien M, Tan C, Hongo JA, de Sauvage F, Plowman G, Yan M. Inhibition of Dll4 signalling inhibits tumour growth by deregulating angiogenesis. Nature. 2006;444(7122):1083-1087. PMid:17183323
  46. Yan M, Callahan CA, Beyer JC, Allamneni KP, Zhang G, Ridgway JB, Niessen K, Plowman GD. Chronic DLL4 blockade induces vascular neoplasms. Nature. 2010;463(7282):E6-7. PMid:20147986
  47. Smith DC, Eisenberg PD, Manikhas G, Chugh R, Gubens MA, Stagg RJ, Kapoun AM, Xu L, Dupont J, Sikic B. A phase I dose escalation and expansion study of the anticancer stem cell agent demcizumab (anti-DLL4) in patients with previously treated solid tumors. Clin Cancer Res. 2014;20(24):6295-6303. PMid:25324140
  48. Chiorean EG, LoRusso P, Strother RM, Diamond JR, Younger A, Messersmith WA, Adriaens L, Liu L, Kao RJ, DiCioccio AT, Kostic A, Leek R, Harris A, Jimeno A. A Phase I First-in-Human Study of Enoticumab (REGN421), a Fully Human Delta-like Ligand 4 (Dll4) Monoclonal Antibody in Patients with Advanced Solid Tumors. Clin Cancer Res. 2015;21(12):2695-2703. PMid:25724527
  49. Weng AP, Ferrando AA, Lee W, Morris JPt, Silverman LB, Sanchez-Irizarry C, Blacklow SC, Look AT, Aster JC. Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia. Science. 2004;306(5694):269-271. PMid:15472075
  50. De Keersmaecker K, Lahortiga I, Mentens N, Folens C, Van Neste L, Bekaert S, Vandenberghe P, Odero MD, Marynen P, Cools J. In vitro validation of gamma-secretase inhibitors alone or in combination with other anti-cancer drugs for the treatment of T-cell acute lymphoblastic leukemia. Haematologica. 2008;93(4):533-542. PMid:18322257
  51. Palomero T, Barnes KC, Real PJ, Glade Bender JL, Sulis ML, Murty VV, Colovai AI, Balbin M, Ferrando AA. CUTLL1, a novel human T-cell lymphoma cell line with t(7;9) rearrangement, aberrant NOTCH1 activation and high sensitivity to gamma-secretase inhibitors. Leukemia. 2006;20(7):1279-1287. PMid:16688224
  52. O'Neil J, Calvo J, McKenna K, Krishnamoorthy V, Aster JC, Bassing CH, Alt FW, Kelliher M, Look AT. Activating Notch1 mutations in mouse models of T-ALL. Blood. 2006;107(2):781-785. PMid:16166587 PMCid:PMC1895623
  53. Deangelo DJ, Stone RM, Silverman LB, Stock W, Attar EC, Fearen I, Dallob A, Matthews C, Stone J, Freedman SJ, Aster J. A phase I clinical trial of the notch inhibitor MK-0752 in patients with T-cell acute lymphoblastic leukemia/lymphoma (T-ALL) and other leukemias. J Clin Onc. 2006;24(18S):6585.
  54. Milano J, McKay J, Dagenais C, Foster-Brown L, Pognan F, Gadient R, Jacobs RT, Zacco A, Greenberg B, Ciaccio PJ. Modulation of notch processing by gamma-secretase inhibitors causes intestinal goblet cell metaplasia and induction of genes known to specify gut secretory lineage differentiation. Toxicological sciences : an official journal of the Society of Toxicology. 2004;82(1):341-358. PMid:15319485
  55. Real PJ, Tosello V, Palomero T, Castillo M, Hernando E, de Stanchina E, Sulis ML, Barnes K, Sawai C, Homminga I, Meijerink J, Aifantis I, Basso G, Cordon-Cardo C, Ai W, Ferrando A. Gamma-secretase inhibitors reverse glucocorticoid resistance in T cell acute lymphoblastic leukemia. Nat Med. 2009;15(1):50-58. PMid:19098907 PMCid:PMC2692090
  56. Real PJ, Ferrando AA. NOTCH inhibition and glucocorticoid therapy in T-cell acute lymphoblastic leukemia. Leukemia. 2009;23(8):1374-1377. PMid:19357700 PMCid:PMC2814171
  57. Aster JC, Blacklow SC. Targeting the Notch pathway: twists and turns on the road to rational therapeutics. J Clin Oncol. 2012;30(19):2418-2420. PMid:22585704
  58. Cullion K, Draheim KM, Hermance N, Tammam J, Sharma VM, Ware C, Nikov G, Krishnamoorthy V, Majumder PK, Kelliher MA. Targeting the Notch1 and mTOR pathways in a mouse T-ALL model. Blood. 2009;113(24):6172-6181. PMid:19246562 PMCid:PMC2699237
  59. Extance A. Alzheimer's failure raises questions about disease-modifying strategies. Nat Rev Drug Discov. 2010;9(10):749-751. PMid:20885394
  60. Nicolas M, Wolfer A, Raj K, Kummer JA, Mill P, van Noort M, Hui CC, Clevers H, Dotto GP, Radtke F. Notch1 functions as a tumor suppressor in mouse skin. Nature genetics. 2003;33(3):416-421. PMid:12590261
  61. Demehri S, Turkoz A, Kopan R. Epidermal Notch1 loss promotes skin tumorigenesis by impacting the stromal microenvironment. Cancer Cell. 2009;16(1):55-66. PMid:19573812 PMCid:PMC2705757
  62. Wang NJ, Sanborn Z, Arnett KL, Bayston LJ, Liao W, Proby CM, Leigh IM, Collisson EA, Gordon PB, Jakkula L, Pennypacker S, Zou Y, Sharma M, North JP, Vemula SS, Mauro TM, Neuhaus IM, Leboit PE, Hur JS, Park K, Huh N, Kwok PY, Arron ST, Massion PP, Bale AE, Haussler D, Cleaver JE, Gray JW, Spellman PT, South AP, Aster JC, Blacklow SC, Cho RJ. Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma. Proc Natl Acad Sci U S A. 2011;108(43):17761-17766. PMid:22006338 PMCid:PMC3203814
  63. Wei P, Walls M, Qiu M, Ding R, Denlinger RH, Wong A, Tsaparikos K, Jani JP, Hosea N, Sands M, Randolph S, Smeal T. Evaluation of selective gamma-secretase inhibitor PF- 03084014 for its antitumor efficacy and gastrointestinal safety to guide optimal clinical trial design. Mol Cancer Ther. 2010;9(6):1618-1628. PMid:20530712
  64. Lopez-Guerra M, Xargay-Torrent S, Rosich L, Montraveta A, Roldan J, Matas-Cespedes A, Villamor N, Aymerich M, Lopez-Otin C, Perez-Galan P, Roue G, Campo E, Colomer D. The gamma-secretase inhibitor PF-03084014 combined with fludarabine antagonizes migration, invasion and angiogenesis in NOTCH1-mutated CLL cells. Leukemia. 2015;29(1):96-106. PMid:24781018
  65. Papayannidis C, DeAngelo DJ, Stock W, Huang B, Shaik MN, Cesari R, Zheng X, Reynolds JM, English PA, Ozeck M, Aster JC, Kuo F, Huang D, Lira PD, McLachlan KR, Kern KA, Garcia-Manero G, Martinelli G. A Phase 1 study of the novel gamma-secretase inhibitor PF-03084014 in patients with T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma. Blood Cancer J. 2015;5:e350. PMid:26407235 PMCid:PMC4648526
  66. Zweidler-McKay P DD, Douer D, et al. The safety and activity of BMS-906024, a gamma secretase inhibitor (GSI) with anti-notch activity, in patients with relapsed T-cell acute lymphoblastic leukemia (T-ALL): initial results of a phase I trial [abstract]. Blood. 2014;121(21):Abstract 968.
  67. Secchiero P, Voltan R, Rimondi E, Melloni E, Athanasakis E, Tisato V, Gallo S, Rigolin GM, Zauli G. The gamma-secretase inhibitors enhance the anti-leukemic activity of ibrutinib in B-CLL cells. Oncotarget. 2017;8(35):59235-59245. PMid:28938632 PMCid:PMC5601728
  68. Bai XC, Yan C, Yang G, Lu P, Ma D, Sun L, Zhou R, Scheres SHW, Shi Y. An atomic structure of human gamma-secretase. Nature. 2015;525(7568):212-217. PMid:26280335 PMCid:PMC4568306
  69. Hayashi I, Takatori S, Urano Y, Miyake Y, Takagi J, Sakata-Yanagimoto M, Iwanari H, Osawa S, Morohashi Y, Li T, Wong PC, Chiba S, Kodama T, Hamakubo T, Tomita T, Iwatsubo T. Neutralization of the gamma-secretase activity by monoclonal antibody against extracellular domain of nicastrin. Oncogene. 2012;31(6):787-798. PMid:21725355 PMCid:PMC4058788
  70. Walker ES, Martinez M, Wang J, Goate A. Conserved residues in juxtamembrane region of the extracellular domain of nicastrin are essential for gamma-secretase complex formation. J Neurochem. 2006;98(1):300-309. PMid:16805816
  71. Previs RA, Coleman RL, Harris AL, Sood AK. Molecular pathways: translational and therapeutic implications of the Notch signaling pathway in cancer. Clin Cancer Res. 2015;21(5):955-961. PMid:25388163 PMCid:PMC4333206
  72. Ran Y, Hossain F, Pannuti A, Lessard CB, Ladd GZ, Jung JI, Minter LM, Osborne BA, Miele L, Golde TE. gamma-Secretase inhibitors in cancer clinical trials are pharmacologically and functionally distinct. EMBO Mol Med. 2017;9(7):950-966. PMid:28539479 PMCid:PMC5494507
  73. Palomero T, Sulis ML, Cortina M, Real PJ, Barnes K, Ciofani M, Caparros E, Buteau J, Brown K, Perkins SL, Bhagat G, Agarwal AM, Basso G, Castillo M, Nagase S, Cordon- Cardo C, Parsons R, Zuniga-Pflucker JC, Dominguez M, Ferrando AA. Mutational loss of PTEN induces resistance to NOTCH1 inhibition in T-cell leukemia. Nat Med. 2007;13(10):1203-1210. PMid:17873882 PMCid:PMC2600418
  74. Palomero T, Dominguez M, Ferrando AA. The role of the PTEN/AKT Pathway in NOTCH1-induced leukemia. Cell Cycle. 2008;7(8):965-970. PMid:18414037 PMCid:PMC2600414
  75. Knoechel B, Roderick JE, Williamson KE, Zhu J, Lohr JG, Cotton MJ, Gillespie SM, Fernandez D, Ku M, Wang H, Piccioni F, Silver SJ, Jain M, Pearson D, Kluk MJ, Ott CJ, Shultz LD, Brehm MA, Greiner DL, Gutierrez A, Stegmaier K, Kung AL, Root DE, Bradner JE, Aster JC, Kelliher MA, Bernstein BE. An epigenetic mechanism of resistance to targeted therapy in T cell acute lymphoblastic leukemia. Nature genetics. 2014.
  76. Roti G, Carlton A, Ross KN, Markstein M, Pajcini K, Su AH, Perrimon N, Pear WS, Kung AL, Blacklow SC, Aster JC, Stegmaier K. Complementary genomic screens identify SERCA as a therapeutic target in NOTCH1 mutated cancer. Cancer Cell. 2013;23(3):390- 405. PMid:23434461 PMCid:PMC3709972
  77. Corsello SM, Roti G, Ross KN, Chow KT, Galinsky I, DeAngelo DJ, Stone RM, Kung AL, Golub TR, Stegmaier K. Identification of AML1-ETO modulators by chemical genomics. Blood. 2009;113(24):6193-6205. PMid:19377049 PMCid:PMC2699238
  78. Roti G, Stegmaier K. New Approaches to Target T-ALL. Frontiers in oncology. 2014;4:170. PMid:25072021 PMCid:PMC4085879
  79. Roti G, Stegmaier K. Genetic and proteomic approaches to identify cancer drug targets. Br J Cancer. 2012;106(2):254-261. PMid:22166799 PMCid:PMC3262130
  80. Frumm SM, Fan ZP, Ross KN, Duvall JR, Gupta S, VerPlank L, Suh BC, Holson E, Wagner FF, Smith WB, Paranal RM, Bassil CF, Qi J, Roti G, Kung AL, Bradner JE, Tolliday N, Stegmaier K. Selective HDAC1/HDAC2 inhibitors induce neuroblastoma differentiation. Chemistry & biology. 2013;20(5):713-725. PMid:23706636 PMCid:PMC3919449
  81. Banerji V, Frumm SM, Ross KN, Li LS, Schinzel AC, Hahn CK, Kakoza RM, Chow KT, Ross L, Alexe G, Tolliday N, Inguilizian H, Galinsky I, Stone RM, DeAngelo DJ, Roti G, Aster JC, Hahn WC, Kung AL, Stegmaier K. The intersection of genetic and chemical genomic screens identifies GSK-3alpha as a target in human acute myeloid leukemia. J Clin Invest. 2012;122(3):935-947. PMid:22326953 PMCid:PMC3287215
  82. Iniguez AB, Alexe G, Wang EJ, Roti G, Patel S, Chen L, Kitara S, Conway A, Robichaud AL, Stolte B, Bandopadhayay P, Goodale A, Pantel S, Lee Y, Cheff DM, Hall MD, Guha R, Davis MI, Menard M, Nasholm N, Weiss WA, Qi J, Beroukhim R, Piccioni F, Johannessen C, Stegmaier K. Resistance to Epigenetic-Targeted Therapy Engenders Tumor Cell Vulnerabilities Associated with Enhancer Remodeling. Cancer Cell. 2018;34(6):922-938 e927. PMid:30537514
  83. Antonello ZA, Hsu N, Bhasin M, Roti G, Joshi M, Van Hummelen P, Ye E, Lo AS, Karumanchi SA, Bryke CR, Nucera C. Vemurafenib-resistance via de novo RBM genes mutations and chromosome 5 aberrations is overcome by combined therapy with palbociclib in thyroid carcinoma with BRAF(V600E). Oncotarget. 2017;8(49):84743- 84760. PMid:29156680 PMCid:PMC5689570
  84. Place AE, Pikman Y, Stevenson KE, Harris MH, Pauly M, Sulis ML, Hijiya N, Gore L, Cooper TM, Loh ML, Roti G, Neuberg DS, Hunt SK, Orloff-Parry S, Stegmaier K, Sallan SE, Silverman LB. Phase I trial of the mTOR inhibitor everolimus in combination with multi-agent chemotherapy in relapsed childhood acute lymphoblastic leukemia. Pediatr Blood Cancer. 2018;65(7):e27062. PMid:29603593
  85. Aster JC, Pear WS, Blacklow SC. Notch signaling in leukemia. Annu Rev Pathol. 2008;3:587-613. PMid:18039126 PMCid:PMC5934586
  86. Stegmaier K, Ross KN, Colavito SA, O'Malley S, Stockwell BR, Golub TR. Gene expression-based high-throughput screening(GE-HTS) and application to leukemia differentiation. Nature genetics. 2004;36(3):257-263. PMid:14770183
  87. Periz G, Fortini ME. Ca(2+)-ATPase function is required for intracellular trafficking of the Notch receptor in Drosophila. EMBO J. 1999;18(21):5983-5993. PMid:10545110 PMCid:PMC1171664
  88. Lytton J, Westlin M, Hanley MR. Thapsigargin inhibits the sarcoplasmic or endoplasmic reticulum Ca-ATPase family of calcium pumps. J Biol Chem. 1991;266(26):17067-17071.
  89. Mahalingam D, Cetnar J, Wilding G, Denmeade S, Sarantopoulos J, Kurman M, Carducci M. Abstract B244: A first-in-human phase 1 clinical study of G-202, a thapsigargin-based Prostate-Specific Membrane Antigen (PSMA) activated prodrug, in patients with advanced solid tumors. Molecular Cancer Therapeutics. 2013;12(11 Supplement):B244.
  90. Doan NT, Paulsen ES, Sehgal P, Moller JV, Nissen P, Denmeade SR, Isaacs JT, Dionne CA, Christensen SB. Targeting thapsigargin towards tumors. Steroids. 2015;97:2-7. PMid:25065587 PMCid:PMC4696022
  91. Christensen SB, Skytte DM, Denmeade SR, Dionne C, Moller JV, Nissen P, Isaacs JT. A Trojan horse in drug development: targeting of thapsigargins towards prostate cancer cells. Anti-cancer agents in medicinal chemistry. 2009;9(3):276-294. PMid:19275521
  92. Roti G, Qi J, Kitara S, Sanchez-Martin M, Saur Conway A, Varca AC, Su A, Wu L, Kung AL, Ferrando AA, Bradner JE, Stegmaier K. Leukemia-specific delivery of mutant NOTCH1 targeted therapy. The Journal of experimental medicine. 2017. PMid:29158376 PMCid:PMC5748843
  93. De Ford C, Heidersdorf B, Haun F, Murillo R, Friedrich T, Borner C, Merfort I. The clerodane diterpene casearin J induces apoptosis of T-ALL cells through SERCA inhibition, oxidative stress, and interference with Notch1 signaling. Cell Death Dis. 2016;7:e2070. PMid:26821066 PMCid:PMC4816186
  94. Aridoss G, Zhou B, Hermanson DL, Bleeker NP, Xing C. Structure-activity relationship (SAR) study of ethyl 2-amino-6-(3,5-dimethoxyphenyl)-4-(2-ethoxy-2-oxoethyl)-4H- chromene-3-carboxylate (CXL017) and the potential of the lead against multidrug resistance in cancer treatment. Journal of medicinal chemistry. 2012;55(11):5566-5581. PMid:22582991 PMCid:PMC6518390
  95. Bleeker NP, Cornea RL, Thomas DD, Xing C. A novel SERCA inhibitor demonstrates synergy with classic SERCA inhibitors and targets multidrug-resistant AML. Mol Pharm. 2013;10(11):4358-4366. PMid:24079514 PMCid:PMC3946399
  96. Roti G RKN, Ferrando A.A., Blacklow S.C., Aster J, Stegmaier K. Expression-Based Screen Identifies the Calcium Channel Antagonist Bepridil as a Notch1 Modulator in T- ALL. . Blood. 2009;114:366.
  97. Baldoni S, Del Papa B, Dorillo E, Aureli P, De Falco F, Rompietti C, Sorcini D, Varasano E, Cecchini D, Zei T, Di Tommaso A, Rosati E, Alexe G, Roti G, Stegmaier K, Di Ianni M, Falzetti F, Sportoletti P. Bepridil exhibits anti-leukemic activity associated with NOTCH1 pathway inhibition in chronic lymphocytic leukemia. Int J Cancer. 2018;143(4):958-970. PMid:29508386 PMCid:PMC6055653
  98. Stahl M, Uemura K, Ge C, Shi S, Tashima Y, Stanley P. Roles of Pofut1 and O-fucose in mammalian Notch signaling. J Biol Chem. 2008;283(20):13638-13651. PMid:18347015 PMCid:PMC2376238
  99. McMillan BJ, Zimmerman B, Egan ED, Lofgren M, Xu X, Hesser A, Blacklow SC. Structure of human POFUT1, its requirement in ligand-independent oncogenic Notch signaling, and functional effects of Dowling-Degos mutations. Glycobiology. 2017;27(8):777-786. PMid:28334865 PMCid:PMC5881682
  100. Koyama D, Kikuchi J, Hiraoka N, Wada T, Kurosawa H, Chiba S, Furukawa Y. Proteasome inhibitors exert cytotoxicity and increase chemosensitivity via transcriptional repression of Notch1 in T-cell acute lymphoblastic leukemia. Leukemia. 2014;28(6):1216- 1226. PMid:24301524 PMCid:PMC4051216
  101. Bertaina A, Vinti L, Strocchio L, Gaspari S, Caruso R, Algeri M, Coletti V, Gurnari C, Romano M, Cefalo MG, Girardi K, Trevisan V, Bertaina V, Merli P, Locatelli F. The combination of bortezomib with chemotherapy to treat relapsed/refractory acute lymphoblastic leukaemia of childhood. Br J Haematol. 2017;176(4):629-636. PMid:28116786
  102. Hubmann R, Duchler M, Schnabl S, Hilgarth M, Demirtas D, Mitteregger D, Holbl A, Vanura K, Le T, Look T, Schwarzmeier JD, Valent P, Jager U, Shehata M. NOTCH2 links protein kinase C delta to the expression of CD23 in chronic lymphocytic leukaemia (CLL) cells. Br J Haematol. 2010;148(6):868-878. PMid:19995395
  103. Hubmann R, Schwarzmeier JD, Shehata M, Hilgarth M, Duechler M, Dettke M, Berger R. Notch2 is involved in the overexpression of CD23 in B-cell chronic lymphocytic leukemia. Blood. 2002;99(10):3742-3747. PMid:11986231
  104. Pahler JC, Ruiz S, Niemer I, Calvert LR, Andreeff M, Keating M, Faderl S, McConkey DJ. Effects of the proteasome inhibitor, bortezomib, on apoptosis in isolated lymphocytes obtained from patients with chronic lymphocytic leukemia. Clin Cancer Res. 2003;9(12):4570-4577.
  105. Masdehors P, Merle-Beral H, Magdelenat H, Delic J. Ubiquitin-proteasome system and increased sensitivity of B-CLL lymphocytes to apoptotic death activation. Leuk Lymphoma. 2000;38(5-6):499-504. PMid:10953970
  106. Duechler M, Shehata M, Schwarzmeier JD, Hoelbl A, Hilgarth M, Hubmann R. Induction of apoptosis by proteasome inhibitors in B-CLL cells is associated with downregulation of CD23 and inactivation of Notch2. Leukemia. 2005;19(2):260-267. PMid:15565166
  107. Arkwright R, Pham TM, Zonder JA, Dou QP. The preclinical discovery and development of bortezomib for the treatment of mantle cell lymphoma. Expert Opin Drug Discov. 2017;12(2):225-235. PMid:27917682 PMCid:PMC5520581
  108. Pham LV, Tamayo AT, Yoshimura LC, Lo P, Ford RJ. Inhibition of constitutive NF-kappa B activation in mantle cell lymphoma B cells leads to induction of cell cycle arrest and apoptosis. J Immunol. 2003;171(1):88-95. PMid:12816986
  109. Manni S, Brancalion A, Mandato E, Tubi LQ, Colpo A, Pizzi M, Cappellesso R, Zaffino F, Di Maggio SA, Cabrelle A, Marino F, Zambello R, Trentin L, Adami F, Gurrieri C, Semenzato G, Piazza F. Protein kinase CK2 inhibition down modulates the NF-kappaB and STAT3 survival pathways, enhances the cellular proteotoxic stress and synergistically boosts the cytotoxic effect of bortezomib on multiple myeloma and mantle cell lymphoma cells. PLoS One. 2013;8(9):e75280. PMid:24086494 PMCid:PMC3785505
  110. Weigert O, Pastore A, Rieken M, Lang N, Hiddemann W, Dreyling M. Sequence- dependent synergy of the proteasome inhibitor bortezomib and cytarabine in mantle cell lymphoma. Leukemia. 2007;21(3):524-528. PMid:17268531
  111. Perez-Galan P, Roue G, Villamor N, Montserrat E, Campo E, Colomer D. The proteasome inhibitor bortezomib induces apoptosis in mantle-cell lymphoma through generation of ROS and Noxa activation independent of p53 status. Blood. 2006;107(1):257-264. PMid:16166592
  112. Weigert O, Weidmann E, Mueck R, Bentz M, von Schilling C, Rohrberg R, Jentsch-Ullrich K, Hiddemann W, Dreyling M. A novel regimen combining high dose cytarabine and bortezomib has activity in multiply relapsed and refractory mantle cell lymphoma - long- term results of a multicenter observation study. Leuk Lymphoma. 2009;50(5):716-722. PMid:19347767
  113. Hutter G, Rieken M, Pastore A, Weigert O, Zimmermann Y, Weinkauf M, Hiddemann W, Dreyling M. The proteasome inhibitor bortezomib targets cell cycle and apoptosis and acts synergistically in a sequence-dependent way with chemotherapeutic agents in mantle cell lymphoma. Ann Hematol. 2012;91(6):847-856. PMid:22231280
  114. Heider U, von Metzler I, Kaiser M, Rosche M, Sterz J, Rotzer S, Rademacher J, Jakob C, Fleissner C, Kuckelkorn U, Kloetzel PM, Sezer O. Synergistic interaction of the histone deacetylase inhibitor SAHA with the proteasome inhibitor bortezomib in mantle cell lymphoma. Eur J Haematol. 2008;80(2):133-142. PMid:18005386
  115. Qu FL, Xia B, Li SX, Tian C, Yang HL, Li Q, Wang YF, Yu Y, Zhang YZ. Synergistic suppression of the PI3K inhibitor CAL-101 with bortezomib on mantle cell lymphoma growth. Cancer Biol Med. 2015;12(4):401-408.
  116. Alinari L, White VL, Earl CT, Ryan TP, Johnston JS, Dalton JT, Ferketich AK, Lai R, Lucas DM, Porcu P, Blum KA, Byrd JC, Baiocchi RA. Combination bortezomib and rituximab treatment affects multiple survival and death pathways to promote apoptosis in mantle cell lymphoma. MAbs. 2009;1(1):31-40. PMid:20046572 PMCid:PMC2715189
  117. Moellering RE, Cornejo M, Davis TN, Del Bianco C, Aster JC, Blacklow SC, Kung AL, Gilliland DG, Verdine GL, Bradner JE. Direct inhibition of the NOTCH transcription factor complex. Nature. 2009;462(7270):182-188. PMid:19907488 PMCid:PMC2951323
  118. Weber D, Bauer M, Murone M, Lehal R, Bourquin J-P, Frismantas V, Radtke F. 411 PPharmacological activity of CB-103: An oral pan-NOTCH inhibitor with a novel mode of action. Annals of Oncology. 2017;28(suppl_5). PMid:28184416 PMCid:PMC5452071
  119. Spriano F, Tarantelli C, Arribas A, Gaudio E, Cascione L, Aresu L, Zucca E, Rossi D, Stathis A, Murone M, Weber D, Lehal R, Radtke F, Bertoni F. Abstract B061: Targeting lymphomas with the novel first-in-class pan-NOTCH transcription inhibitor CB-103. Molecular Cancer Therapeutics. 2018;17:B061-B061.
  120. Garcia JMP, Cortés J, Stathis A, Mous R, López-Miranda E, Azaro A, Genta S, Nuciforo P, Vivancos A, Ferrarotto R, Bertoni F, Rossi D, Burr NS, Schönborn-Kellenberger O, Jorga K, Beni L, Lehal R, Bauer M, Weber D, Garralda E. First-in-human phase 1-2A study of CB-103, an oral Protein-Protein Interaction Inhibitor targeting pan-NOTCH signalling in advanced solid tumors and blood malignancies. Journal of Clinical Oncology. 2018;36(15_suppl):TPS2619-TPS2619.