Abstract
<div>Abstract<p>Genome-wide association studies (GWAS) have revealed numerous genetic loci associated with colorectal cancer risk, but the mechanisms underlying these loci have not been comprehensively elucidated. In this study, we performed a GWAS meta-analysis with a two-stage replication strategy by combining eight colorectal cancer cohorts encompassing 7,186 cases and 8,512 controls in Chinese populations, accompanied by an evaluation encompassing 29,832 cases and 406,694 controls in European populations. The genetic variant rs505706 A>G, located at chr1q44 in the upstream region of catsper channel auxiliary subunit epsilon (<i>CATSPERE</i>), was associated with colorectal cancer risk and exhibited genome-wide significance (OR, 0.73; 95% confidence interval, 0.67–0.80; <i>P</i> = 9.75 × 10<sup>–12</sup>). Cell line and animal models were applied to assess the biological function of the genetic risk variant and the corresponding susceptibility gene. Genetically, the G allele of rs505706 resulted in long-range regulatory effects, reducing the binding affinity of POU2F1 for the <i>CATSPERE</i> promoter and thus abolishing the inhibitory effect of POU2F1 on <i>CATSPERE</i> transcription. Phenotypically, <i>CATSPERE</i> upregulation attenuated tumor growth in both colorectal cancer cells and xenograft models. Mechanistically, <i>CATSPERE</i> promoted calcium ion influx and apoptotic pathway activity. In zebrafish models, <i>CATSPERE</i> exerted pleiotropic effects, enhancing the progression of colorectal cancer. Collectively, these findings highlight a colorectal cancer susceptibility locus that acts to remotely modulate the activity of <i>CATSPERE</i>, a gene that mediates multiple functions involved in colorectal tumorigenesis and progression.</p>Significance:<p>A GWAS meta-analysis identifies a novel susceptibility locus harboring a genetic risk variant that mediates pleiotropic biological effects in colorectal tumorigenesis and progression.</p></div>
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