Dual‐target inhibitors of bromodomain and extra‐terminal proteins in cancer: A review from medicinal chemistry perspectives-Reference-Cited by-同舟云学术

Dual‐target inhibitors of bromodomain and extra‐terminal proteins in cancer: A review from medicinal chemistry perspectives

Published:2021-10-11 Issue: Volume: Page:
ISSN:0198-6325
Container-title:Medicinal Research Reviews
language:en
Short-container-title:Medicinal Research Reviews

Author:

Feng Lu¹,Wang Guan¹,Chen Yi²,He Gu¹^ORCID,Liu Bo¹^ORCID,Liu Jie¹,Chiang Cheng‐Ming³⁴⁵^ORCID,Ouyang Liang¹^ORCID

Affiliation:

1. State Key Laboratory of Biotherapy and Cancer Center, Innovation Center of Nursing Research, Nursing Key Laboratory of Sichuan Province, National Clinical Research Center for Geriatrics, West China Hospital, and Collaborative Innovation Center of Biotherapy Sichuan University Chengdu China

2. State Key Laboratory of Biotherapy and Cancer Center and Department of Gastrointestinal Surgery, West China Hospital Sichuan University, and Collaborative Innovation Center for Biotherapy Chengdu China

3. Simmons Comprehensive Cancer Center University of Texas Southwestern Medical Center Dallas Texas USA

4. Department of Pharmacology University of Texas Southwestern Medical Center Dallas Texas USA

5. Department of Biochemistry University of Texas Southwestern Medical Center Dallas Texas USA

Funder

National Natural Science Foundation of China

Cancer Prevention and Research Institute of Texas

Publisher

Wiley

Subject

Drug Discovery,Pharmacology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/med.21859

Reference164 articles.

1. The Double Bromodomain-containing Chromatin Adaptor Brd4 and Transcriptional Regulation

2. Histone Recognition and Large-Scale Structural Analysis of the Human Bromodomain Family

3. Epigenetic protein families: a new frontier for drug discovery

4. Disrupting Acetyl-Lysine Recognition: Progress in the Development of Bromodomain Inhibitors

5. BET Bromodomain Inhibition as a Therapeutic Strategy to Target c-Myc

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