Genome-wide scan of the effect of common nsSNPs on colorectal cancer survival outcome

A partir des données du registre écossais des cancers colorectaux incluant 1 939 patients, et menée à l'échelle du génome, cette étude identifie des polymorphismes à simple nucléotide non synonymes en association avec la survie

Résumé en anglais

Background : We conducted a genome-wide scan to identify non-synonymous SNPs (nsSNPs) that might influence survival after a diagnosis of colorectal cancer (CRC).

Methods : We genotyped 7679 nsSNPs in 1939 Scottish patients from the Scottish Colorectal Cancer Study recruited soon after a CRC diagnosis and prospectively followed for survival outcomes. All-cause and CRC-specific survival analyses were conducted using Cox proportional hazard models adjusted for stage, age and sex for all cancer cases, after cancer type stratification and assuming additive and recessive models of inheritance. For all the SNPs that had a p-value < 0.10 a meta-analysis was performed combining the results of the discovery set and a replication set of 899 Scottish CRC patients. The p-value threshold of significance was set as at p < 10−8.

Results : 897 and 894 nsSNPs were associated with all-cause and CRC-specific mortality, respectively, at a p-value level < 0.10 in the discovery set. Meta-analysis of the results from the discovery and replication sets was performed overall and for cancers of colon and rectum separately and none of the variants reached a p-value < 10−8.

Conclusions : This large scale well-powered analysis demonstrates that common nsSNPs are not associated with CRC prognosis overall.