Literature DB >> 30542529

Targeting Brd4 for cancer therapy: inhibitors and degraders.

Yingchao Duan1, Yuanyuan Guan1, Wenping Qin1, Xiaoyu Zhai1, Bin Yu2, Hongmin Liu2.   

Abstract

Bromodomain-containing protein 4 (Brd4) plays an important role in mediating the expression of genes involved in cancers and non-cancer diseases such as inflammatory diseases and acute heart failure. Inactivating Brd4 or downregulating its expression inhibits cancer development, leading to the current interest in Brd4 as a promising anticancer drug target. Numerous Brd4 inhibitors have been studied in recent years and some of them are currently in various phases of clinical trials. Recently, selective degradation of target proteins by small bifunctional molecules (PROTACs) has emerged as an attractive drug discovery approach owing to the advantages it could offer over traditional small-molecule inhibitors. A number of Brd4 degraders have been reported and showed more efficient anticancer activities than just protein inhibition. In this review, we will discuss recent findings in the discovery and development of small-molecule inhibitors and degraders that target Brd4 as a potential anticancer agent.

Entities:  

Year:  2018        PMID: 30542529      PMCID: PMC6238758          DOI: 10.1039/c8md00198g

Source DB:  PubMed          Journal:  Medchemcomm        ISSN: 2040-2503            Impact factor:   3.597


  105 in total

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Authors:  Panagis Filippakopoulos; Stefan Knapp
Journal:  Nat Rev Drug Discov       Date:  2014-04-22       Impact factor: 84.694

2.  Exploitation of Castration-Resistant Prostate Cancer Transcription Factor Dependencies by the Novel BET Inhibitor ABBV-075.

Authors:  Emily J Faivre; Denise Wilcox; Xiaoyu Lin; Paul Hessler; Maricel Torrent; Wei He; Tamar Uziel; Daniel H Albert; Keith McDaniel; Warren Kati; Yu Shen
Journal:  Mol Cancer Res       Date:  2016-10-05       Impact factor: 5.852

3.  Fragment-based discovery of bromodomain inhibitors part 2: optimization of phenylisoxazole sulfonamides.

Authors:  Paul Bamborough; Hawa Diallo; Jonathan D Goodacre; Laurie Gordon; Antonia Lewis; Jonathan T Seal; David M Wilson; Michael D Woodrow; Chun-Wa Chung
Journal:  J Med Chem       Date:  2012-01-11       Impact factor: 7.446

4.  Structure-Based Discovery and Optimization of Benzo[ d]isoxazole Derivatives as Potent and Selective BET Inhibitors for Potential Treatment of Castration-Resistant Prostate Cancer (CRPC).

Authors:  Maofeng Zhang; Yan Zhang; Ming Song; Xiaoqian Xue; Junjian Wang; Chao Wang; Cheng Zhang; Chenchang Li; Qiuping Xiang; Lingjiao Zou; Xishan Wu; Chun Wu; Baijun Dong; Wei Xue; Yulai Zhou; Hongwu Chen; Donghai Wu; Ke Ding; Yong Xu
Journal:  J Med Chem       Date:  2018-04-03       Impact factor: 7.446

5.  Therapeutic targeting of BET bromodomain proteins in castration-resistant prostate cancer.

Authors:  Irfan A Asangani; Vijaya L Dommeti; Xiaoju Wang; Rohit Malik; Marcin Cieslik; Rendong Yang; June Escara-Wilke; Kari Wilder-Romans; Sudheer Dhanireddy; Carl Engelke; Mathew K Iyer; Xiaojun Jing; Yi-Mi Wu; Xuhong Cao; Zhaohui S Qin; Shaomeng Wang; Felix Y Feng; Arul M Chinnaiyan
Journal:  Nature       Date:  2014-04-23       Impact factor: 49.962

6.  Y08060: A Selective BET Inhibitor for Treatment of Prostate Cancer.

Authors:  Qiuping Xiang; Yan Zhang; Jiaguo Li; Xiaoqian Xue; Chao Wang; Ming Song; Cheng Zhang; Rui Wang; Chenchang Li; Chun Wu; Yulai Zhou; Xiaohong Yang; Guohui Li; Ke Ding; Yong Xu
Journal:  ACS Med Chem Lett       Date:  2018-02-13       Impact factor: 4.345

7.  Fragment-based drug discovery of 2-thiazolidinones as inhibitors of the histone reader BRD4 bromodomain.

Authors:  Lele Zhao; Danyan Cao; Tiantian Chen; Yingqing Wang; Zehong Miao; Yechun Xu; Wuyan Chen; Xin Wang; Yanlian Li; Zhiyan Du; Bing Xiong; Jian Li; Chunyan Xu; Naixia Zhang; Jianhua He; Jingkang Shen
Journal:  J Med Chem       Date:  2013-05-14       Impact factor: 7.446

8.  AZD3514: a small molecule that modulates androgen receptor signaling and function in vitro and in vivo.

Authors:  Sarah A Loddick; Sarah J Ross; Andrew G Thomason; David M Robinson; Graeme E Walker; Tom P J Dunkley; Sandra R Brave; Nicola Broadbent; Natalie C Stratton; Dawn Trueman; Elizabeth Mouchet; Fadhel S Shaheen; Vivien N Jacobs; Marie Cumberbatch; Joanne Wilson; Rhys D O Jones; Robert H Bradbury; Alfred Rabow; Luke Gaughan; Chris Womack; Simon T Barry; Craig N Robson; Susan E Critchlow; Stephen R Wedge; A Nigel Brooks
Journal:  Mol Cancer Ther       Date:  2013-07-16       Impact factor: 6.261

9.  Bromodomain 4 activation predicts breast cancer survival.

Authors:  Nigel P S Crawford; Jude Alsarraj; Luanne Lukes; Renard C Walker; Jennifer S Officewala; Howard H Yang; Maxwell P Lee; Keiko Ozato; Kent W Hunter
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-21       Impact factor: 11.205

10.  Discovery of a Small-Molecule Degrader of Bromodomain and Extra-Terminal (BET) Proteins with Picomolar Cellular Potencies and Capable of Achieving Tumor Regression.

Authors:  Bing Zhou; Jiantao Hu; Fuming Xu; Zhuo Chen; Longchuan Bai; Ester Fernandez-Salas; Mei Lin; Liu Liu; Chao-Yie Yang; Yujun Zhao; Donna McEachern; Sally Przybranowski; Bo Wen; Duxin Sun; Shaomeng Wang
Journal:  J Med Chem       Date:  2017-03-24       Impact factor: 7.446

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  32 in total

Review 1.  Targeting epigenetic protein-protein interactions with small-molecule inhibitors.

Authors:  Brian M Linhares; Jolanta Grembecka; Tomasz Cierpicki
Journal:  Future Med Chem       Date:  2020-06-19       Impact factor: 3.808

Review 2.  Validation of the epigenetic reader bromodomain-containing protein 4 (BRD4) as a therapeutic target for treatment of airway remodeling.

Authors:  Allan R Brasier; Jia Zhou
Journal:  Drug Discov Today       Date:  2019-11-13       Impact factor: 7.851

3.  An inhibitor of BRD4, GNE987, inhibits the growth of glioblastoma cells by targeting C-Myc and S100A16.

Authors:  Liya Ma; Gen Li; Tianquan Yang; Li Zhang; Xinxin Wang; Xiaowen Xu; Hong Ni
Journal:  Cancer Chemother Pharmacol       Date:  2022-10-12       Impact factor: 3.288

Review 4.  Molecular relation between biological stress and carcinogenesis.

Authors:  Katarzyna Rakoczy; Wojciech Szlasa; Natalia Sauer; Jolanta Saczko; Julita Kulbacka
Journal:  Mol Biol Rep       Date:  2022-05-24       Impact factor: 2.742

Review 5.  Bivalent Ligands for Protein Degradation in Drug Discovery.

Authors:  Marcel Scheepstra; Koen F W Hekking; Luc van Hijfte; Rutger H A Folmer
Journal:  Comput Struct Biotechnol J       Date:  2019-01-25       Impact factor: 7.271

6.  Targeting bromodomain-containing protein 4 (BRD4) inhibits MYC expression in colorectal cancer cells.

Authors:  C Otto; S Schmidt; C Kastner; S Denk; J Kettler; N Müller; C T Germer; E Wolf; P Gallant; A Wiegering
Journal:  Neoplasia       Date:  2019-11-14       Impact factor: 5.715

Review 7.  Repurposing old drugs as new inhibitors of the ubiquitin-proteasome pathway for cancer treatment.

Authors:  Huanjie Yang; Xin Chen; Kai Li; Hassan Cheaito; Qianqian Yang; Guojun Wu; Jinbao Liu; Q Ping Dou
Journal:  Semin Cancer Biol       Date:  2019-12-26       Impact factor: 15.707

8.  The poly(ADP-ribosyl)ation of BRD4 mediated by PARP1 promoted pathological cardiac hypertrophy.

Authors:  Zhenzhen Li; Zhen Guo; Rui Lan; Sidong Cai; Zhirong Lin; Jingyan Li; Junjian Wang; Zhuoming Li; Peiqing Liu
Journal:  Acta Pharm Sin B       Date:  2020-12-14       Impact factor: 11.413

Review 9.  Targeting CDK9 for Anti-Cancer Therapeutics.

Authors:  Ranadip Mandal; Sven Becker; Klaus Strebhardt
Journal:  Cancers (Basel)       Date:  2021-05-01       Impact factor: 6.639

10.  PCAF-mediated acetylation of ISX recruits BRD4 to promote epithelial-mesenchymal transition.

Authors:  Li-Ting Wang; Kwei-Yan Liu; Wen-Yih Jeng; Cheng-Ming Chiang; Chee-Yin Chai; Shyh-Shin Chiou; Ming-Shyang Huang; Kazunari K Yokoyama; Shen-Nien Wang; Shau-Ku Huang; Shih-Hsien Hsu
Journal:  EMBO Rep       Date:  2020-01-07       Impact factor: 8.807

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