Open AccessCopy number variation analysis of m 6 A regulators identified METTL3 as a prognostic and immune‐related biomarker in bladder cancer
Author(s) -
Wang Xiaoshuai,
Yu Jingwei,
Chen Jinbao,
Hou Yingdong,
Du Zefeng,
Huang Haoyang,
Tang Siqi,
Han Yueyin,
Ding Changhai,
Xue Zhicheng
Publication year - 2021
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.3981
Subject(s) - copy number variation , biology , gene , immune system , cancer research , immune checkpoint , genetics , genome , immunotherapy
Purpose Growing evidence has demonstrated an indispensable role for N 6 ‐methyladenosine (m 6 A) in human diseases, but the copy number variations (CNVs) of m 6 A regulatory genes in bladder cancer (BLCA) remains largely unknown. Methods We investigated the CNVs on all known m 6 A regulatory genes using the Cancer Genome Atlas (TCGA) database. The association between CNV events and clinicopathological as well as molecular characteristics of BLCA patients were explored. Gene set enrichment analysis (GSEA) was implemented to reveal relative cellular processes. Association between m 6 A regulatory genes and immune infiltrates was analyzed by The Tumor Immune Estimation Resource (TIMER) database. Results CNV events of m 6 A regulatory genes were frequently observed in BLCA. CNVs of METTL3, METTL14, and METTL16 correlated with molecular characteristics of BLCA patients including TP53 mutation. CNVs of METTL3 associated with the overall survival (OS) of BLCA patients. METTL3 was also associated with several cancer‐related cellular processes, including mitotic spindle assembly, G2/M checkpoint, and E2F targets signaling pathway. Besides, the CNVs of m 6 A regulatory genes were correlated with specific kinds of immune infiltrates. Conclusions There are significant correlations between m 6 A regulatory genes with CNVs and clinicopathological characteristics. METTL3 with CNVs were associated with the immune infiltrates and performed as a prognostic marker in BLCA.