Notch Inhibition in Cancer: Challenges and Opportunities

被引:12
作者
Fabbro, Doriano [3 ]
Bauer, Michael [1 ]
Murone, Maximilien [2 ]
Lehal, Rajwinder [3 ,4 ]
机构
[1] Cellestia, Basel, Switzerland
[2] Genentech Inc, San Francisco, CA 94080 USA
[3] Cellestia Biotech, Basel, Switzerland
[4] Cellestia Biotech AG, Hochbergerstr 60C, CH-4057 Basel, Switzerland
关键词
CB-103; Cancer; Notch; gamma-Secretase inhibitors; CD8(-) DENDRITIC CELLS; ZONE B-CELLS; BREAST-CANCER; PHYLOGENETIC ANALYSIS; DOSE-ESCALATION; ACTIVATION; TRANSCRIPTION; ROLES; GENE; INACTIVATION;
D O I
10.2533/chimia.2020.779
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Notch is a key oncogenic pathway in several human cancers and to date, no targeted treatment of Notch activated cancers is available to patients. Therapeutic targeting of Notch has been an unresolved challenge due to severe on-target dose limiting toxicities associated with pan-Notch inhibition by either gamma-secretase inhibitors or receptor/ligand targeting MAbs. At Cellestia Biotech, we have identified novel series of small molecule inhibitors of the Notch transcription complex. These molecules act as pan-Notch inhibitors and do not cause toxicities commonly associated with first- and second- generation Notch inhibitors currently tested in the clinic, thus providing a novel and unique opportunity to address a high unmet medical need. Our lead molecule, CB-103 is currently being investigated in Phase-1 dose escalation in cancer patients. Cellestia Biothech is further expanding its medicinal chemistry activities advancing the development of novel molecules for targeting transcription factors in cancer as well as non-cancer indications.
引用
收藏
页码:779 / 783
页数:5
相关论文
共 67 条
[1]   Notch promotes recurrence of dormant tumor cells following HER2/neu-targeted therapy [J].
Abravanel, Daniel L. ;
Belka, George K. ;
Pan, Tien-chi ;
Pant, Dhruv K. ;
Collins, Meredith A. ;
Sterner, Christopher J. ;
Chodosh, Lewis A. .
JOURNAL OF CLINICAL INVESTIGATION, 2015, 125 (06) :2484-2496
[2]   Therapeutic modulation of Notch signalling - are we there yet? [J].
Andersson, Emma R. ;
Lendahl, Urban .
NATURE REVIEWS DRUG DISCOVERY, 2014, 13 (05) :359-380
[3]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[4]   Deletion-based mechanisms of Notch1 activation in T-ALL: key roles for RAG recombinase and a conserved internal translational start site in Notch1 [J].
Ashworth, Todd D. ;
Pear, Warren S. ;
Chiang, Mark Y. ;
Blacklow, Stephen C. ;
Mastio, Jerome ;
Xu, Lanwei ;
Kelliher, Michelle ;
Kastner, Philippe ;
Chan, Susan ;
Aster, Jon C. .
BLOOD, 2010, 116 (25) :5455-5464
[5]   The Varied Roles of Notch in Cancer [J].
Aster, Jon C. ;
Pear, Warren S. ;
Blacklow, Stephen C. .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 12, 2017, 12 :245-275
[6]   The Small Molecule IMR-1 Inhibits the Notch Transcriptional Activation Complex to Suppress Tumorigenesis [J].
Astudillo, Luisana ;
Da Silva, Thiago G. ;
Wang, Zhiqiang ;
Han, Xiaoqing ;
Jin, Ke ;
VanWye, Jeffrey ;
Zhu, Xiaoxia ;
Weaver, Kelly ;
Oashi, Taiji ;
Lopes, Pedro E. M. ;
Orton, Darren ;
Neitzel, Leif R. ;
Lee, Ethan ;
Landgraf, Ralf ;
Robbins, David J. ;
MacKerell, Alexander D., Jr. ;
Capobianco, Anthony J. .
CANCER RESEARCH, 2016, 76 (12) :3593-3603
[7]   A multi-arm phase I dose escalating study of an oral NOTCH inhibitor BMS-986115 in patients with advanced solid tumours [J].
Aung, Kyaw L. ;
El-Khoueiry, Anthony B. ;
Gelmon, Karen ;
Tran, Ben ;
Bajaj, Gaurav ;
He, Bing ;
Chen, Tian ;
Zhu, Lili ;
Poojary, Sharath ;
Basak, Shashwati ;
Qi, Zhenhao ;
Spreafico, Anna ;
Fischer, Bruce S. ;
Desai, Jayesh .
INVESTIGATIONAL NEW DRUGS, 2018, 36 (06) :1026-1036
[8]   Notch Signaling Regulates Mammary Stem Cell Function and Luminal Cell-Fate Commitment [J].
Bouras, Toula ;
Pal, Bhupinder ;
Vaillant, Francois ;
Harburg, Gwyndolen ;
Asselin-Labat, Marie-Liesse ;
Oakes, Samantha R. ;
Lindeman, Geoffrey J. ;
Visvader, Jane E. .
CELL STEM CELL, 2008, 3 (04) :429-441
[9]   A novel proteolytic cleavage involved in Notch signaling:: The role of the disintegrin-metalloprotease TACE [J].
Brou, C ;
Logeat, F ;
Gupta, N ;
Bessia, C ;
LeBail, O ;
Doedens, JR ;
Cumano, A ;
Roux, P ;
Black, RA ;
Israël, A .
MOLECULAR CELL, 2000, 5 (02) :207-216
[10]   The canonical Notch/RBP-J signaling pathway controls the balance of cell lineages in mammary epithelium during pregnancy [J].
Buono, Krista D. ;
Robinson, Gertraud W. ;
Martin, Cyril ;
Shi, Shaolin ;
Stanley, Pamela ;
Tanigaki, Kenji ;
Honjo, Tasuku ;
Hennighausen, Lothar .
DEVELOPMENTAL BIOLOGY, 2006, 293 (02) :565-580