Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory), Guangzhou, 510005, China.
Institute of Hematology, School of Medicine, Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University, Guangzhou, 510632, China.
J Hematol Oncol. 2020 Aug 27;13(1):117. doi: 10.1186/s13045-020-00951-w.
N-methyladenosine (mA) is the most abundant mRNA modification and is catalyzed by the methyltransferase complex, in which methyltransferase-like 3 (METTL3) is the sole catalytic subunit. Accumulating evidence in recent years reveals that METTL3 plays key roles in a variety of cancer types, either dependent or independent on its mA RNA methyltransferase activity. While the roles of mA modifications in cancer have been extensively reviewed elsewhere, the critical functions of METTL3 in various types of cancer, as well as the potential targeting of METTL3 as cancer treatment, have not yet been highlighted. Here we summarize our current understanding both on the oncogenic and tumor-suppressive functions of METTL3, as well as the underlying molecular mechanisms. The well-documented protein structure of the METTL3/METTL14 heterodimer provides the basis for potential therapeutic targeting, which is also discussed in this review.
N6-甲基腺苷(m6A)是最丰富的 mRNA 修饰,由甲基转移酶复合物催化,其中甲基转移酶样蛋白 3(METTL3)是唯一的催化亚基。近年来越来越多的证据表明,METTL3 在多种癌症类型中发挥关键作用,其依赖或不依赖于其 m6A RNA 甲基转移酶活性。虽然 m6A 修饰在癌症中的作用已在其他地方广泛综述,但 METTL3 在各种类型癌症中的关键功能以及将 METTL3 作为癌症治疗的潜在靶点尚未得到强调。在这里,我们总结了我们目前对 METTL3 的致癌和肿瘤抑制功能以及潜在的分子机制的理解。METTL3/METTL14 异二聚体的有充分文献记录的蛋白质结构为潜在的治疗靶向提供了基础,这也在本综述中进行了讨论。