| Literature DB >> 27484627 |
Jinlian Wei1,2, Yingrui Yang1,2, Mengchen Lu1,2, Yonghua Lei1,2, Lili Xu1,2, Zhengyu Jiang1,2, Xiaoli Xu1,2, Xiaoke Guo1,2, Xiaojin Zhang1,2,3, Haopeng Sun1,2,4, Qidong You1,2.
Abstract
Hypoxia-inducible factor-1 (HIF-1), a heterodimeric (containing α and β subunits) transcription factor, is involved in hypoxia response pathway that regulates the expression of many tumorrelated genes. The stabilized HIF-1 heterodimer couples to the general co-activators p300/CBP (CREB binding protein), forming an active transcription factor to initiate hypoxic responses. Inhibiting the transcription factor-coactivator HIF-1α-p300/CBP interaction represents an attractive approach for blocking hypoxia pathway in tumors. Recently, diverse HIF-1α-p300/CBP inhibitors have been designed and their anti-tumor activities have been evaluated. The developments of inhibitors of HIF-1α- p300/CBP are discussed in this review. An outline of structures and biological activities of these inhibitors can be traced, along with the approaches for inhibitors discovery. The challenges in identifying novel and selective potent inhibitors of HIF-1α-p300/CBP are also put forward. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.Entities:
Keywords: Anticancer; HIF-1α/p300 inhibitors; cancer therapy; hypoxia response pathway; hypoxia-inducible factor-1; p300/CREB binding protein
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Year: 2018 PMID: 27484627 DOI: 10.2174/1389557516666160630124938
Source DB: PubMed Journal: Mini Rev Med Chem ISSN: 1389-5575 Impact factor: 3.862