Karanth Archana Venkataramana, Maniswami Radhika Radha, Prashanth Seema, Govindaraj Hemalatha, Padmavathy Ramya, Jegatheesan Sooriya Kumar, Mullangi Ramesh, Rajagopal Sriram
a Bioinformatics, Jubilant Biosys Ltd. , Bangalore , India.
Expert Opin Ther Targets. 2017 Mar;21(3):319-331. doi: 10.1080/14728222.2017.1279604. Epub 2017 Jan 20.
Epigenetic changes lead to aberrant gene expression in cancer. SETDB1, a histone lysine methyltransferase plays an important role in methylation and gene silencing. Aberrant histone methylation at H3K9 by SETDB1 promotes silencing of tumor suppressor genes and thus contributes to carcinogenesis. Recent studies indicate that SETDB1 is abnormally expressed in various human cancer conditions which contributed to enhanced tumor growth and metastasis. Hence, SETDB1 appears to be a promising epigenetic target for therapeutic intervention. Areas covered: In this article, the structural features, localization and functions of SETDB1 are reviewed. Also, an overview of the role of SETDB1 in cancer and other disease mechanisms, the currently studied inhibitors for SETDB1 are mentioned. Expert opinion: Silencing of tumor suppressor genes due to excessive trimethylation at H3K9 by amplified SETDB1 levels is found in various cancerous conditions. Since epigenetic changes are reversible, SETDB1 holds promise as an important therapeutic target for cancer. Therefore, a better understanding of the role of SETDB1 and its interaction with various proteins in cancer-related mechanisms along with therapeutic interventions specific for SETDB1 may improve targeted cancer therapy.
表观遗传变化导致癌症中基因表达异常。SETDB1是一种组蛋白赖氨酸甲基转移酶,在甲基化和基因沉默中起重要作用。SETDB1介导的H3K9异常组蛋白甲基化促进肿瘤抑制基因沉默,从而促进肿瘤发生。最近的研究表明,SETDB1在多种人类癌症中异常表达,这有助于肿瘤生长和转移增强。因此,SETDB1似乎是一个有前景的表观遗传治疗靶点。涵盖领域:本文综述了SETDB1的结构特征、定位和功能。此外,还概述了SETDB1在癌症和其他疾病机制中的作用,以及目前研究的SETDB1抑制剂。专家观点:在各种癌症情况下,发现由于SETDB1水平升高导致H3K9过度三甲基化,从而使肿瘤抑制基因沉默。由于表观遗传变化是可逆的,SETDB1有望成为癌症的重要治疗靶点。因此,更好地了解SETDB1在癌症相关机制中的作用及其与各种蛋白质的相互作用,以及针对SETDB1的治疗干预措施,可能会改善靶向癌症治疗。