An updated patent review of BRD4 degraders

被引:3
作者
Ma, Zonghui [1 ]
Zhang, Cun [1 ]
Bolinger, Andrew A. [1 ]
Zhou, Jia [1 ]
机构
[1] Univ Texas Med Branch UTMB, Dept Pharmacol & Toxicol, Chem Biol Program, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
Bromodomain-containing protein 4 (BRD4); epigenetic regulation; disease therapeutics; inhibitors; degraders; proteolysis-targeting chimera (PROTAC); molecular glue (MG); protein degradation; BET BROMODOMAIN INHIBITORS; P-TEFB; HISTONE ACETYLTRANSFERASE; TARGETING BROMODOMAIN; PROTEIN-DEGRADATION; THERAPEUTIC TARGET; STRUCTURAL BASIS; DRUG DISCOVERY; CHROMATIN; CANCER;
D O I
10.1080/13543776.2024.2400166
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
IntroductionBromodomain-containing protein 4 (BRD4), an important epigenetic reader, is closely associated with the pathogenesis and development of many diseases, including various cancers, inflammation, and infectious diseases. Targeting BRD4 inhibition or protein elimination with small molecules represents a promising therapeutic strategy, particularly for cancer therapy.Areas coveredThe recent advances of patented BRD4 degraders were summarized. The challenges, opportunities, and future directions for developing novel potent and selective BRD4 degraders are also discussed. The patents of BRD4 degraders were searched using the SciFinder and Cortellis Drug Discovery Intelligence database.Expert opinionBRD4 degraders exhibit superior efficacy and selectivity to BRD4 inhibitors, given their unique mechanism of protein degradation instead of protein inhibition. Excitingly, RNK05047 is now in phase I/II clinical trials, indicating that selective BRD4 protein degradation may offer a viable therapeutic strategy, particularly for cancer. Targeting BRD4 with small-molecule degraders provides a promising approach with the potential to overcome therapeutic resistance for treating various BRD4-associated diseases.
引用
收藏
页码:929 / 951
页数:23
相关论文
共 50 条
  • [31] Hijacking the E3 Ubiquitin Ligase Cereblon to Efficiently Target BRD4
    Lu, Jing
    Qian, Yimin
    Altieri, Martha
    Dong, Hanqing
    Wang, Jing
    Raina, Kanak
    Hines, John
    Winkler, James D.
    Crew, Andrew P.
    Coleman, Kevin
    Crews, Craig M.
    CHEMISTRY & BIOLOGY, 2015, 22 (06): : 755 - 763
  • [32] BRD4 inhibitors block telomere elongation
    Wang, Steven
    Pike, Alexandra M.
    Lee, Stella S.
    Strong, Margaret A.
    Connelly, Carla J.
    Greider, Carol W.
    NUCLEIC ACIDS RESEARCH, 2017, 45 (14) : 8403 - 8410
  • [33] BRD4 Protein as a Target for Lung Cancer and Hematological Cancer Therapy: A Review
    Zhang, Mengmeng
    Li, Yingbo
    Zhang, Zilong
    Zhang, Xin
    Wang, Wei
    Song, Xiaomei
    Zhang, Dongdong
    CURRENT DRUG TARGETS, 2023, 24 (14) : 1079 - 1092
  • [34] BRD4 as a Therapeutic Target in Pulmonary Diseases
    Guo, Xia
    Olajuyin, Ayobami
    Tucker, Torry A.
    Idell, Steven
    Qian, Guoqing
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (17)
  • [35] BRD4: an effective target for organ fibrosis
    Wei, Qun
    Gan, Cailing
    Sun, Meng
    Xie, Yuting
    Liu, Hongyao
    Xue, Taixiong
    Deng, Conghui
    Mo, Chunheng
    Ye, Tinghong
    BIOMARKER RESEARCH, 2024, 12 (01)
  • [36] BET degraders reveal BRD4 disruption of 7SK and P-TEFb is critical for effective reactivation of latent HIV in CD4+T-cells
    Turner, Anne-Marie W.
    Bashore, Frances M.
    Falcinelli, Shane D.
    Fox, Joshua A.
    Keller, Alana L.
    Fenton, Anthony D.
    Geyer, Renee F.
    Allard, Brigitte
    Kirchherr, Jennifer L.
    Archin, Nancie M.
    James, Lindsey I.
    Margolis, David M.
    JOURNAL OF VIROLOGY, 2025, 99 (04)
  • [37] Preparation data of the bromodomains BRD3(1), BRD3(2), BRD4(1), and BRPF1B and crystallization of BRD4(1)-inhibitor complexes
    Huegle, Martin
    Lucas, Xavier
    Weitzel, Gerhard
    Ostrovskyi, Dmytro
    Breit, Bernhard
    Gerhardt, Stefan
    Schmidtkunz, Karin
    Jung, Manfred
    Schuele, Roland
    Einsle, Oliver
    Guenther, Stefan
    Wohlwend, Daniel
    DATA IN BRIEF, 2016, 7 : 1370 - 1374
  • [38] Chromatin Landscape of the IRF Genes and Role of the Epigenetic Reader BRD4
    Bachu, Mahesh
    Dey, Anup
    Ozato, Keiko
    JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2016, 36 (07) : 470 - 475
  • [39] BRD4 sustains p63 transcriptional program in keratinocytes
    Foffi, E.
    Violante, A.
    Pecorari, R.
    Lena, A. M.
    Rugolo, F.
    Melino, G.
    Candi, E.
    BIOLOGY DIRECT, 2024, 19 (01)
  • [40] Dynamic Chromatin Targeting of BRD4 Stimulates Cardiac Fibroblast Activation
    Stratton, Matthew S.
    Bagchi, Rushita A.
    Felisbino, Marina B.
    Hirsch, Rachel A.
    Smith, Harrison E.
    Riching, Andrew S.
    Enyart, Blake Y.
    Koch, Keith A.
    Cavasin, Maria A.
    Alexanian, Michael
    Song, Kunhua
    Qi, Jun
    Lemieux, Madeleine E.
    Srivastava, Deepak
    Lam, Maggie P. Y.
    Haldar, Saptarsi M.
    Lin, Charles Y.
    McKinsey, Timothy A.
    CIRCULATION RESEARCH, 2019, 125 (07) : 662 - 677