结直肠癌
基因
N6-甲基腺苷
生物
癌症研究
微阵列
基因表达
转录组
腺癌
下调和上调
信使核糖核酸
组织微阵列
微阵列分析技术
癌症
遗传学
甲基化
甲基转移酶
作者
Xin Liu,Liwen Liu,Zihui Dong,Jianhao Li,Yan Yu,Xiaolong Chen,Fang Ren,Guangying Cui,Ranran Sun
出处
期刊:PubMed
日期:2019-01-01
卷期号:11 (7): 3972-3991
被引量:117
摘要
Colorectal cancer (CRC), including colon adenocarcinoma (COAD) and rectal adenocarcinoma (READ), is one of the most prevalent malignancies worldwide. N6-methyladenosine (m6A) is a ubiquitous RNA modification that plays a vital role in human tumors, but its expression patterns and prognostic value in CRC have not yet been determined. Here, we first used the Cancer Genome Atlas (TCGA), the Gene Expression Omnibus (GEO) and the Human Protein Atlas (HPA) databases and a tissue microarray (TMA) cohort to verify the expression of m6A-related genes at the mRNA and protein levels. We found that most m6A-related genes were substantially upregulated in tumor tissues compared with normal tissues, but METTL14, YTHDF3 and ALKBH5 were downregulated in CRC. There was no obvious difference in FTO. In addition, WTAP, METTL16, HNRNPC and YTHDC1 were abundantly expressed in COAD but not in READ. Moreover, immunofluorescence (IF) analyses of SW480 and HCT116 cells showed that most of the m6A-related proteins were expressed in the nucleus and cytoplasm. Survival analysis demonstrated that the expression levels of METTL3, METTL14, METTL16, FTO and ALKBH5 were associated with the clinical outcomes of CRC patients. Taken together, all the results revealed that m6A-related genes were dysregulated in CRC and might play a significant role in the progression of CRC.
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