Arginine methylation of ALKBH5 by PRMT6 promotes breast tumorigenesis via LDHA-mediated glycolysis

被引:4
|
作者
Han, Xue [1 ]
Ren, Chune [1 ]
Jiang, Aifang [1 ]
Sun, Yonghong [2 ]
Lu, Jiayi [1 ]
Ling, Xi [1 ]
Lu, Chao [1 ]
Yu, Zhenhai [1 ]
机构
[1] Weifang Med Univ, Affiliated Hosp, Dept Reprod Med, Weifang 261053, Peoples R China
[2] Weifang Med Univ, Affiliated Hosp, Dept Pathol, Weifang 261053, Peoples R China
基金
中国国家自然科学基金;
关键词
PRMT6; ALKBH5; N6-methyladenosine; glycolysis; tumor growth; CANCER; PROGRESSION; H3K4;
D O I
10.1007/s11684-023-1028-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ALKBH5 is a master regulator of N6-methyladenosine (m6A) modification, which plays a crucial role in many biological processes. Here, we show that ALKBH5 is required for breast tumor growth. Interestingly, PRMT6 directly methylates ALKBH5 at R283, which subsequently promotes breast tumor growth. Furthermore, arginine methylation of ALKBH5 by PRMT6 increases LDHA RNA stability via m6A demethylation, leading to increased aerobic glycolysis. Moreover, PRMT6-mediated ALKBH5 arginine methylation is confirmed in PRMT6-knockout mice. Collectively, these findings identify a PRMT6-ALKBH5-LDHA signaling axis as a novel target for the treatment of breast cancer.
引用
收藏
页码:344 / 356
页数:13
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