Literature DB >> 30289209

Bromodomain Drug Discovery - the Past, the Present, and the Future.

Mehrosh Pervaiz1, Pankaj Mishra1, Stefan Günther1.   

Abstract

With the bromodomain (BRD) inhibitor JQ1, a remarkable success story of BRD4 as a novel drug target has been set off that yielded many anti-cancer drugs that are now in clinical trials. But not all of the great prospects of BRDs as drug targets may become true. First evaluations of ongoing clinical trials revealed that treatment with BET-inhibitors can be accompanied with significant toxic side effects and the validation of the therapeutic benefit of BET-inhibitors compared to existing therapies is still pending. New strategies that may overcome possible obstacles in BRD drug discovery include combination therapies with other agents, dual target inhibitors, and proteolysis targeting chimeras (PROTACs). Furthermore, non-BET proteins seem promising drug targets as well. Most recently, BRDs have been identified as putative targets to treat parasitic diseases such as malaria. Milestones in BRD drug discovery are reviewed and promising new developments are evaluated.
© 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  BET-inhibitors; PROTACs; bromodomains; drug discovery; dual target inhibitors; epigenetics

Mesh:

Substances:

Year:  2018        PMID: 30289209     DOI: 10.1002/tcr.201800074

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  26 in total

Review 1.  BET Epigenetic Reader Proteins in Cardiovascular Transcriptional Programs.

Authors:  Patricia Cristine Borck; Lian-Wang Guo; Jorge Plutzky
Journal:  Circ Res       Date:  2020-04-23       Impact factor: 17.367

2.  Systematically Mitigating the p38α Activity of Triazole-based BET Inhibitors.

Authors:  Angela S Carlson; Huarui Cui; Anand Divakaran; Jorden A Johnson; Ryan M Brunner; William C K Pomerantz; Joseph J Topczewski
Journal:  ACS Med Chem Lett       Date:  2019-08-02       Impact factor: 4.345

3.  The novel BET degrader, QCA570, is highly active against the growth of human NSCLC cells and synergizes with osimertinib in suppressing osimertinib-resistant EGFR-mutant NSCLC cells.

Authors:  Chaoyuan Liu; Luxi Qian; Karin A Vallega; Guangzhi Ma; Dan Zong; Luxiao Chen; Shaomeng Wang; Suresh R Ramalingam; Zhaohui Qin; Shi-Yong Sun
Journal:  Am J Cancer Res       Date:  2022-02-15       Impact factor: 6.166

4.  Bromodomain-containing-protein-4 and cyclin-dependent-kinase-9 inhibitors interact synergistically in vitro and combined treatment reduces post-traumatic osteoarthritis severity in mice.

Authors:  T Fukui; J H N Yik; B Doyran; J Davis; A K Haudenschild; I E Adamopoulos; L Han; D R Haudenschild
Journal:  Osteoarthritis Cartilage       Date:  2020-10-23       Impact factor: 6.576

5.  Degradation of BRD4 - a promising treatment approach not only for hematologic but also for solid cancer.

Authors:  Karin Bauer; Anna S Berghoff; Matthias Preusser; Gerwin Heller; Christoph C Zielinski; Peter Valent; Thomas W Grunt
Journal:  Am J Cancer Res       Date:  2021-02-01       Impact factor: 6.166

Review 6.  Selective Targeting of Epigenetic Readers and Histone Deacetylases in Autoimmune and Inflammatory Diseases: Recent Advances and Future Perspectives.

Authors:  Mohammed Ghiboub; Ahmed M I Elfiky; Menno P J de Winther; Nicola R Harker; David F Tough; Wouter J de Jonge
Journal:  J Pers Med       Date:  2021-04-23

7.  BET inhibitor suppresses migration of human hepatocellular carcinoma by inhibiting SMARCA4.

Authors:  Hae In Choi; Ga Yeong An; Mina Baek; Eunyoung Yoo; Jin Choul Chai; Young Seek Lee; Kyoung Hwa Jung; Young Gyu Chai
Journal:  Sci Rep       Date:  2021-06-03       Impact factor: 4.379

8.  JMJD6 Is a Druggable Oxygenase That Regulates AR-V7 Expression in Prostate Cancer.

Authors:  Alec Paschalis; Jonathan Welti; Adam Sharp; Johann S de Bono; Antje J Neeb; Wei Yuan; Ines Figueiredo; Rita Pereira; Ana Ferreira; Ruth Riisnaes; Daniel Nava Rodrigues; Juan M Jiménez-Vacas; Soojin Kim; Takuma Uo; Patrizio Di Micco; Anthony Tumber; Md Saiful Islam; Marc A Moesser; Martine Abboud; Akane Kawamura; Bora Gurel; Rossitza Christova; Veronica S Gil; Lorenzo Buroni; Mateus Crespo; Susana Miranda; Maryou B Lambros; Suzanne Carreira; Nina Tunariu; Andrea Alimonti; Bissan Al-Lazikani; Christopher J Schofield; Stephen R Plymate
Journal:  Cancer Res       Date:  2021-02-15       Impact factor: 13.312

9.  Covalent-Fragment Screening of BRD4 Identifies a Ligandable Site Orthogonal to the Acetyl-Lysine Binding Sites.

Authors:  Michael D Olp; Daniel J Sprague; Christopher J Goetz; Stefan G Kathman; Sarah L Wynia-Smith; Shifali Shishodia; Steven B Summers; Ziyang Xu; Alexander V Statsyuk; Brian C Smith
Journal:  ACS Chem Biol       Date:  2020-03-23       Impact factor: 5.100

10.  Fms-like tyrosine kinase 3-internal tandem duplications epigenetically activates checkpoint kinase 1 in acute myeloid leukemia cells.

Authors:  Yudong Zhang; Lingli Yuan
Journal:  Sci Rep       Date:  2021-06-24       Impact factor: 4.379

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