| Literature DB >> 31396313 |
Xin Liu1,2, Liwen Liu1,2, Zihui Dong1,2, Jianhao Li1,2, Yan Yu1,2, Xiaolong Chen1,2, Fang Ren2, Guangying Cui1,2, Ranran Sun1,2,3.
Abstract
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.Entities:
Keywords: Colorectal cancer; TCGA; TMA; m6A; prognosis
Year: 2019 PMID: 31396313 PMCID: PMC6684930
Source DB: PubMed Journal: Am J Transl Res ISSN: 1943-8141 Impact factor: 4.060