Advances in Histone Demethylase KDM3A as a Cancer Therapeutic Target

被引:49
|
作者
Yoo, Jung [1 ]
Jeon, Yu Hyun [1 ]
Cho, Ha Young [1 ]
Lee, Sang Wu [1 ]
Kim, Go Woon [1 ]
Lee, Dong Hoon [1 ]
Kwon, So Hee [1 ,2 ]
机构
[1] Yonsei Univ, Yonsei Inst Pharmaceut Sci, Coll Pharm, Incheon 21983, South Korea
[2] Yonsei Univ, Dept Integrated OM Biomed Sci, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
KDM3A; histone H3K9 demethylase; KDM3; inhibitor; anti-cancer agent; epigenetic agent; LONG NONCODING RNA; HEPATOCELLULAR-CARCINOMA; SUBSTRATE-SPECIFICITY; STRUCTURAL INSIGHTS; CELL-PROLIFERATION; PROSTATE-CANCER; JMJD2; FAMILY; HYPOXIA; INHIBITION; EXPRESSION;
D O I
10.3390/cancers12051098
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lysine-specific histone demethylase 3 (KDM3) subfamily proteins are H3K9me2/me1 histone demethylases that promote gene expression. The KDM3 subfamily primarily consists of four proteins (KDM3A-D). All four proteins contain the catalytic Jumonji C domain (JmjC) at their C-termini, but whether KDM3C has demethylase activity is under debate. In addition, KDM3 proteins contain a zinc-finger domain for DNA binding and an LXXLL motif for interacting with nuclear receptors. Of the KDM3 proteins, KDM3A is especially deregulated or overexpressed in multiple cancers, making it a potential cancer therapeutic target. However, no KDM3A-selective inhibitors have been identified to date because of the lack of structural information. Uncovering the distinct physiological and pathological functions of KDM3A and their structure will give insight into the development of novel selective inhibitors. In this review, we focus on recent studies highlighting the oncogenic functions of KDM3A in cancer. We also discuss existing KDM3A-related inhibitors and review their potential as therapeutic agents for overcoming cancer.
引用
收藏
页数:18
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