| Literature DB >> 34555614 |
Guan-Jun Yang1, Jia Wu2, Liang Miao1, Ming-Hui Zhu1, Qian-Jin Zhou1, Xin-Jiang Lu1, Jian-Fei Lu1, Chung-Hang Leung3, Dik-Lung Ma4, Jiong Chen5.
Abstract
Lysine-specific demethylase 5A (KDM5A, also named RBP2 or JARID1A) is a demethylase that can remove methyl groups from histones H3K4me1/2/3. It is aberrantly expressed in many cancers, where it impedes differentiation and contributes to cancer cell proliferation, cell metastasis and invasiveness, drug resistance, and is associated with poor prognosis. Pharmacological inhibition of KDM5A has been reported to significantly attenuate tumor progression in vitro and in vivo in a range of solid tumors and acute myeloid leukemia. This review will present the structural aspects of KDM5A, its role in carcinogenesis, a comparison of currently available approaches for screening KDM5A inhibitors, a classification of KDM5A inhibitors, and its potential as a drug target in cancer therapy.Entities:
Keywords: Cancer therapy; Drug resistance; Histone methylation; Lysine-specific demethylase 5A; Screening methods
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Year: 2021 PMID: 34555614 DOI: 10.1016/j.ejmech.2021.113855
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514