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组蛋白甲基化在皮肤癌中的作用:组蛋白甲基化修饰酶作为皮肤癌治疗的新靶标。

Role of histone methylation in skin cancers: Histone methylation-modifying enzymes as a new class of targets for skin cancer treatment.

机构信息

Department of Biocosmetics, Sungkyunkwan University, Suwon 16419, Republic of Korea.

Department of Integrative Biotechnology, Sungkyunkwan University, Suwon 16419, Republic of Korea; Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Republic of Korea.

出版信息

Biochim Biophys Acta Rev Cancer. 2023 May;1878(3):188865. doi: 10.1016/j.bbcan.2023.188865. Epub 2023 Feb 24.

Abstract

Histone methylation, one of the most prominent epigenetic modifications, plays a vital role in gene transcription, and aberrant histone methylation levels cause tumorigenesis. Histone methylation is a reversible enzyme-dependent reaction, and histone methyltransferases and demethylases are involved in this reaction. This review addresses the biological and clinical relevance of these histone methylation-modifying enzymes for skin cancer. In particular, the roles of histone lysine methyltransferases, histone arginine methyltransferase, lysine-specific demethylases, and JmjC demethylases in skin cancer are discussed in detail. In addition, we summarize the efficacy of several epigenetic inhibitors targeting histone methylation-modifying enzymes in cutaneous cancers, such as basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and melanoma. In conclusion, we propose histone methylation-modifying enzymes as novel targets for next-generation pharmaceuticals in the treatment of skin cancers and further provide a rationale for the development of epigenetic drugs (epidrugs) that target specific histone methylases/demethylases in cutaneous tumors.

摘要

组蛋白甲基化是最显著的表观遗传修饰之一,在基因转录中起着至关重要的作用,异常的组蛋白甲基化水平会导致肿瘤发生。组蛋白甲基化是一种可逆的酶依赖性反应,涉及组蛋白甲基转移酶和去甲基酶。本综述讨论了这些组蛋白甲基化修饰酶在皮肤癌中的生物学和临床相关性。特别是,详细讨论了组蛋白赖氨酸甲基转移酶、组蛋白精氨酸甲基转移酶、赖氨酸特异性去甲基酶和 JmjC 去甲基酶在皮肤癌中的作用。此外,我们总结了几种针对组蛋白甲基化修饰酶的表观遗传抑制剂在皮肤癌中的疗效,如基底细胞癌 (BCC)、鳞状细胞癌 (SCC) 和黑色素瘤。总之,我们提出组蛋白甲基化修饰酶作为治疗皮肤癌的下一代药物的新靶点,并进一步为开发针对皮肤肿瘤特定组蛋白甲基酶/去甲基酶的表观遗传药物 (epidrugs) 提供了依据。

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