RNA N6-methyladenosine modifications in urological cancers: from mechanism to application

被引:4
|
作者
Yang, Lei [1 ]
Ying, Jianming [2 ,3 ]
Tao, Qian [4 ,5 ]
Zhang, Qian [1 ,6 ]
机构
[1] Peking Univ, Peking Univ First Hosp, Natl Res Ctr Genitourinary Oncol, Dept Urol,Inst Urol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll PUMC, Canc Inst, Dept Pathol, Beijing, Peoples R China
[3] Chinese Acad Med Sci, Canc Hosp, Peking Union Med Coll PUMC, Beijing, Peoples R China
[4] Chinese Univ Hong Kong, Sir YK Pao Ctr Canc, State Key Lab Translat Oncol, Canc Epigenet Lab,Dept Clin Oncol, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Hong Kong, Peoples R China
[6] Peking Univ, Binhai Hosp, Dept Urol, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
METHYLTRANSFERASE METTL3 PROMOTES; DEPENDENT DIOXYGENASE FTO; RENAL-CELL CARCINOMA; PROSTATE-CANCER; BLADDER-CANCER; MESSENGER-RNA; METHYLATION REGULATORS; MALIGNANT PROGRESSION; M(6)A METHYLATION; M6A MODIFICATION;
D O I
10.1038/s41585-023-00851-x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The N-6-methyladenosine (m(6)A) modification is the most common modification of messenger RNAs in eukaryotes and has crucial roles in multiple cancers, including in urological malignancies such as renal cell carcinoma, bladder cancer and prostate cancer. The m(6)A RNA modification is controlled by three types of regulators, including methyltransferases (writers), demethylases (erasers) and RNA-binding proteins (readers), which are responsible for gene regulation at the post-transcriptional level. This Review summarizes the current evidence indicating that aberrant or dysregulated m6A modification is associated with urological cancer development, progression and prognosis. The complex and context-dependent effects of dysregulated m(6)A modifications in urological cancers are described, along with the potential for aberrantly expressed m(6)A regulators to provide valuable diagnostic and prognostic biomarkers as well as new therapeutic targets.
引用
收藏
页码:460 / 476
页数:17
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