Yoo Jung, Jeon Yu Hyun, Cho Ha Young, Lee Sang Wu, Kim Go Woon, Lee Dong Hoon, Kwon So Hee
College of Pharmacy, Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon 21983, Korea.
Department of Integrated OMICS for Biomedical Science, Yonsei University, Seoul 03722, Korea.
Cancers (Basel). 2020 Apr 28;12(5):1098. doi: 10.3390/cancers12051098.
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.
赖氨酸特异性组蛋白去甲基化酶3(KDM3)亚家族蛋白是促进基因表达的H3K9me2/me1组蛋白去甲基化酶。KDM3亚家族主要由四种蛋白(KDM3A-D)组成。这四种蛋白在其C末端均含有催化性的Jumonji C结构域(JmjC),但KDM3C是否具有去甲基化酶活性仍存在争议。此外,KDM3蛋白含有一个用于结合DNA的锌指结构域和一个用于与核受体相互作用的LXXLL基序。在KDM3蛋白中,KDM3A在多种癌症中尤其失调或过表达,使其成为潜在的癌症治疗靶点。然而,由于缺乏结构信息,迄今为止尚未鉴定出KDM3A选择性抑制剂。揭示KDM3A独特的生理和病理功能及其结构将有助于深入了解新型选择性抑制剂的开发。在本综述中,我们重点关注近期突出KDM3A在癌症中致癌功能的研究。我们还讨论了现有的与KDM3A相关的抑制剂,并综述了它们作为克服癌症治疗药物的潜力。