免疫组织化学
腺瘤
结直肠腺瘤
癌变
基因
癌症研究
结直肠癌
生物
信使核糖核酸
基因表达
病理
分子生物学
癌症
医学
遗传学
作者
Dayu Kuai,Shengtao Zhu,Haiyun Shi,Ruichuang Yang,Tong Liu,Hui Liu,Li Min,Shutian Zhang
出处
期刊:Life Sciences
[Elsevier]
日期:2021-02-23
卷期号:273: 119258-119258
被引量:27
标识
DOI:10.1016/j.lfs.2021.119258
摘要
Abstract Background As the most prevalent post-transcriptional mRNA modification in eukaryotes, N6-Methyladenosine (m6A) is closely linked to the occurrence and development of colorectal cancer (CRC). However, there is no systematic evaluation of the expression of m6A regulatory genes in CRC. Methods By analyzing the TCGA database, we identified METTL3, YTHDF1, IGF2BP1, IGF2BP3, EIF3B, HNRNPA2B1 as overexpressed m6A regulators in CRC. After verification by immunohistochemistry (IHC) in 10 CRC cases, YTHDF1, IGF2BP1, IGF2BP3, and EIF3B were identified as potential biomarkers in CRC. Further validation was done by IHC and qRT-PCR in two larger cohorts. Results We identified 6 up-regulated m6A regulatory genes in CRC in TCGA analysis, and verified that YTHDF1, IGF2BP1, IGF2BP3, and EIFB3 were all significantly differentially expressed between CRC and normal tissues by IHC (p Conclusion We evaluted the abnormal expression of m6A regulatory genes during CRC carcinogenesis, and identified four m6A genes (YTHDF1, IGF2BP1, IGF2BP3, and EIF3B) as potential biomarkers of both CRC and adenoma.
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