Genetic variants reshape the m(6)A epitranscriptome and drive transcriptomic reprogramming in colorectal cancer

基因变异重塑m(6)A表观转录组并驱动结直肠癌的转录组重编程

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Abstract

Genome-wide association studies (GWAS) have identified numerous single-nucleotide polymorphisms (SNPs) associated with various diseases, including cancer. However, the mechanisms by which these SNPs contribute to disease susceptibility remain largely unclear. While recent studies have explored the transcriptional impact of disease-associated SNPs, their role in post-transcriptional regulation has been less extensively investigated. In this study, we investigated whether cancer-associated SNPs influence gene expression by altering N6-methyladenosine (m(6)A) RNA methylation. We collected GWAS-identified SNPs across nine cancer types and integrated these with matched tumor and normal m(6)A RNA immunoprecipitation sequencing (m(6)A-seq) and RNA sequencing (RNA-seq) datasets. We first identified differentially methylated m(6)A sites and assessed whether cancer-associated SNPs were enriched within these regions. These analyses revealed that cancer-associated SNPs were significantly enriched within hypermethylated m(6)A regions in colon cancer. Integrative analysis revealed that SNPs enriched in m(6)A-modified regions are associated with altered gene expression and RNA splicing, suggesting that m(6)A methylation mediates the post-transcriptional impact of genetic variants. Experimental validation further confirmed altered gene expression following ALKBH5 knockdown, consistent with patient-derived data. Collectively, our findings support a novel mechanistic connection between genetic variants and RNA methylation-driven transcriptomic regulation in colorectal cancer, underscoring the epitranscriptome as a potential axis of oncogenic control.

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