Ten-Eleven-Translocation Genes in Cancer.

Yadong Wang, Xujun Wang, Jun Lu
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Abstract

The Ten-Eleven-Translocation (TET) family of genes, including TET1, TET2, and TET3, play critical roles in the oxidation of 5-methylcytosine marks in both DNA and RNA, thereby regulating the epigenome and epitranscriptome in cells. These genes are frequently mutated in both hematopoietic malignancies and in solid cancers. TET2, in particular, is one of the most frequently mutated genes in clonal hematopoiesis in the general population, which impacts both the transformation of hematopoietic malignancies and the immune responses in solid tumors. While much has been learned in the 14 years since the discovery of TETs' biochemical function and mutations, many important questions remain. This review covers several aspects of TET-related biology to discuss key yet unanswered questions. What are the functions of different forms of TET mutations found in human cancers? How does TET2 mutation enable pre-malignant hematopoietic expansion? How does TET2 mutation cooperate with partner lesions to cause transformation? And how do TET mutations affect immune responses in solid cancers.

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癌症中的 Ten-Eleven-Translocation 基因
包括 TET1、TET2 和 TET3 在内的 Ten-Eleven-Translocation (TET)家族基因在 DNA 和 RNA 中 5-甲基胞嘧啶标记的氧化过程中发挥着关键作用,从而调节细胞中的表观遗传组和表转录组。在造血恶性肿瘤和实体瘤中,这些基因经常发生突变。特别是 TET2,它是普通人群克隆性造血中最常发生突变的基因之一,对造血恶性肿瘤的转化和实体瘤的免疫反应都有影响。自发现 TETs 的生化功能和突变以来的 14 年中,人们已经了解了很多,但仍有许多重要问题。这篇综述涵盖了 TET 相关生物学的几个方面,讨论了尚未解答的关键问题。在人类癌症中发现的不同形式的 TET 突变有哪些功能?TET2突变如何使恶性前造血扩张?TET2突变如何与伙伴病变合作导致转化?TET突变如何影响实体瘤的免疫反应?
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来源期刊
Cancer treatment and research
Cancer treatment and research Medicine-Oncology
CiteScore
1.00
自引率
0.00%
发文量
11
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