Yale Stem Cell Center, Yale University School of Medicine, New Haven, CT, 06520, USA.
Department of Genetics, Yale University School of Medicine, New Haven, CT, 06510, USA.
Cancer Treat Res. 2023;190:363-373. doi: 10.1007/978-3-031-45654-1_11.
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.
TET 家族基因(包括 TET1、TET2 和 TET3)在 DNA 和 RNA 中 5-甲基胞嘧啶标记的氧化中发挥关键作用,从而调节细胞中的表观基因组和表转录组。这些基因在造血恶性肿瘤和实体瘤中经常发生突变。特别是 TET2,是普通人群中克隆性造血中突变频率最高的基因之一,它既影响造血恶性肿瘤的转化,也影响实体肿瘤中的免疫反应。自发现 TET 的生化功能和突变以来的 14 年中,已经有了很多了解,但仍有许多重要的问题尚未得到解答。这篇综述涵盖了与 TET 相关的生物学的几个方面,以讨论关键但尚未解决的问题。在人类癌症中发现的不同形式的 TET 突变有什么作用?TET2 突变如何使恶性前造血细胞扩张?TET2 突变如何与伙伴病变合作导致转化?以及 TET 突变如何影响实体瘤中的免疫反应。