Literature DB >> 25053499

Small molecules that inhibit Notch signaling.

Gerdien E De Kloe1, Bart De Strooper.   

Abstract

The proteolytic processing of Notch receptors plays a central role in the transduction of Notch signaling, which is involved in a variety of important processes in the body. Abnormal Notch processing has been implicated in a variety of cancers. γ-Secretase is responsible for the third and last cleavage step of Notch receptors. Since γ-secretase plays an important role in Alzheimer's disease, great effort has been spent to develop γ-secretase inhibitors (GSIs). The majority of these inhibitors block γ-secretase nonselectively, which means that these compounds can be used to block Notch cleavage and thereby regulate Notch signaling. In this review we give an overview of the most-used GSIs in the Notch field, together with examples of their use. It is a huge advantage that these drug-like compounds are already optimized for γ-secretase, and some are already being used in clinical trials. However, their nonspecificity has disadvantages as well, since four Notch receptors exist with different sites of expression and different roles in cell signaling and at least four different γ-secretase proteases are involved in their cleavage. It would be worth the effort to screen many GSIs for their selectivity for the different Notch receptors and γ-secretases, in order to obtain interesting tools for further research and-in the end-to develop safer drugs.

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Year:  2014        PMID: 25053499     DOI: 10.1007/978-1-4939-1139-4_23

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  9 in total

1.  Therapeutic inhibition of USP9x-mediated Notch signaling in triple-negative breast cancer.

Authors:  Arushi Jaiswal; Kiichi Murakami; Andrew Elia; Yukiko Shibahara; Susan J Done; Stephen A Wood; Nicholas J Donato; Pamela S Ohashi; Michael Reedijk
Journal:  Proc Natl Acad Sci U S A       Date:  2021-09-21       Impact factor: 11.205

2.  The Small Molecule IMR-1 Inhibits the Notch Transcriptional Activation Complex to Suppress Tumorigenesis.

Authors:  Luisana Astudillo; Thiago G Da Silva; Zhiqiang Wang; Xiaoqing Han; Ke Jin; Jeffrey VanWye; Xiaoxia Zhu; Kelly Weaver; Taiji Oashi; Pedro E M Lopes; Darren Orton; Leif R Neitzel; Ethan Lee; Ralf Landgraf; David J Robbins; Alexander D MacKerell; Anthony J Capobianco
Journal:  Cancer Res       Date:  2016-04-13       Impact factor: 12.701

Review 3.  Notch-ing up knowledge on molecular mechanisms of skin fibrosis: focus on the multifaceted Notch signalling pathway.

Authors:  Angelo Giuseppe Condorelli; May El Hachem; Giovanna Zambruno; Alexander Nystrom; Eleonora Candi; Daniele Castiglia
Journal:  J Biomed Sci       Date:  2021-05-09       Impact factor: 8.410

4.  A phase I trial of the γ-secretase inhibitor MK-0752 in combination with gemcitabine in patients with pancreatic ductal adenocarcinoma.

Authors:  Natalie Cook; Bristi Basu; Donna-Michelle Smith; Aarthi Gopinathan; Jeffry Evans; William P Steward; Daniel Palmer; David Propper; Balaji Venugopal; Mirela Hategan; D Alan Anthoney; Lisa V Hampson; Michael Nebozhyn; David Tuveson; Hayley Farmer-Hall; Helen Turner; Robert McLeod; Sarah Halford; Duncan Jodrell
Journal:  Br J Cancer       Date:  2018-02-13       Impact factor: 7.640

Review 5.  Taming the Notch Transcriptional Regulator for Cancer Therapy.

Authors:  Luca Tamagnone; Serena Zacchigna; Michael Rehman
Journal:  Molecules       Date:  2018-02-15       Impact factor: 4.411

6.  AL101, a gamma-secretase inhibitor, has potent antitumor activity against adenoid cystic carcinoma with activated NOTCH signaling.

Authors:  Renata Ferrarotto; Vasudha Mishra; Elad Herz; Adar Yaacov; Oz Solomon; Rami Rauch; Adi Mondshine; Maria Motin; Tal Leibovich-Rivkin; Matti Davis; Joel Kaye; Christopher R Weber; Le Shen; Alexander T Pearson; Ari J Rosenberg; Xiangying Chen; Alka Singh; Jon C Aster; Nishant Agrawal; Evgeny Izumchenko
Journal:  Cell Death Dis       Date:  2022-08-05       Impact factor: 9.685

7.  RO4929097, a Selective γ-Secretase Inhibitor, Inhibits Subretinal Fibrosis Via Suppressing Notch and ERK1/2 Signaling in Laser-Induced Mouse Model.

Authors:  Chaoyang Zhang; Shiyue Qin; Hai Xie; Qinghua Qiu; Haiyan Wang; Jingting Zhang; Dawei Luo; Jingfa Zhang
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-09-01       Impact factor: 4.925

8.  Monoamine oxidase B is elevated in Alzheimer disease neurons, is associated with γ-secretase and regulates neuronal amyloid β-peptide levels.

Authors:  Sophia Schedin-Weiss; Mitsuhiro Inoue; Lenka Hromadkova; Yasuhiro Teranishi; Natsuko Goto Yamamoto; Birgitta Wiehager; Nenad Bogdanovic; Bengt Winblad; Anna Sandebring-Matton; Susanne Frykman; Lars O Tjernberg
Journal:  Alzheimers Res Ther       Date:  2017-08-01       Impact factor: 6.982

9.  The DLC-1 tumor suppressor is involved in regulating immunomodulation of human mesenchymal stromal /stem cells through interacting with the Notch1 protein.

Authors:  Tao Na; Kehua Zhang; Bao-Zhu Yuan
Journal:  BMC Cancer       Date:  2020-11-04       Impact factor: 4.430

  9 in total

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