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癌症中的SMYD家族:癌症增殖、转移和耐药性的表观遗传调控及分子机制

SMYD family in cancer: epigenetic regulation and molecular mechanisms of cancer proliferation, metastasis, and drug resistance.

作者信息

Han Tae-Su, Kim Dae-Soo, Son Mi-Young, Cho Hyun-Soo

机构信息

Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Republic of Korea.

Korea University of Science and Technology, Daejeon, 34316, Republic of Korea.

出版信息

Exp Mol Med. 2024 Nov;56(11):2325-2336. doi: 10.1038/s12276-024-01326-8. Epub 2024 Nov 1.

Abstract

Epigenetic modifiers (miRNAs, histone methyltransferases (HMTs)/demethylases, and DNA methyltransferases/demethylases) are associated with cancer proliferation, metastasis, angiogenesis, and drug resistance. Among these modifiers, HMTs are frequently overexpressed in various cancers, and recent studies have increasingly identified these proteins as potential therapeutic targets. In this review, we discuss members of the SET and MYND domain-containing protein (SMYD) family that are topics of extensive research on the histone methylation and nonhistone methylation of cancer-related genes. Various members of the SMYD family play significant roles in cancer proliferation, metastasis, and drug resistance by regulating cancer-specific histone methylation and nonhistone methylation. Thus, the development of specific inhibitors that target SMYD family members may lead to the development of cancer treatments, and combination therapy with various anticancer therapeutic agents may increase treatment efficacy.

摘要

表观遗传修饰因子(微小RNA、组蛋白甲基转移酶/去甲基酶以及DNA甲基转移酶/去甲基酶)与癌症的增殖、转移、血管生成及耐药性相关。在这些修饰因子中,组蛋白甲基转移酶在多种癌症中常过度表达,并且最近的研究越来越多地将这些蛋白质确定为潜在的治疗靶点。在本综述中,我们讨论了含SET和MYND结构域蛋白(SMYD)家族的成员,它们是癌症相关基因的组蛋白甲基化和非组蛋白甲基化广泛研究的主题。SMYD家族的各种成员通过调节癌症特异性组蛋白甲基化和非组蛋白甲基化在癌症增殖、转移和耐药性中发挥重要作用。因此,开发靶向SMYD家族成员的特异性抑制剂可能会带来癌症治疗方法的发展,并且与各种抗癌治疗药物的联合治疗可能会提高治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/462c/11611910/0b0fe36aa140/12276_2024_1326_Fig1_HTML.jpg

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