AI Article Synopsis

  • * Overall analysis found no significant association between rs4919510 and cancer risk across all genetic models but noted a reduced risk for colorectal cancer and a potential increased risk for papillary thyroid cancer based on specific genetic models.
  • * The rs4919510 GG genotype was linked to poorer recurrence-free survival among cancer patients, indicating the need for further research on larger populations to confirm these findings.

Article Abstract

The role of rs4919510 polymorphism in microRNA-608 (miR-608) and cancer susceptibility and prognosis remain controversial and debatable. We conducted a meta-analysis of twenty-four eligible publications on the association of rs4919510 polymorphism with cancer risk and/or prognosis. Odds ratios, hazard ratios, and 95% confidence interval were used to investigate the association between this polymorphism and susceptibility, overall survival, and recurrence-free survival of cancer. Overall, eighteen case-control studies and nine cohort studies evaluated the susceptibility and prognostic value of rs4919510 polymorphism in cancer, respectively. Pooled analysis showed that rs4919510 polymorphism was not associated with cancer risk in all five genetic models. When stratifying by different cancer sites, rs4919510 polymorphism was detected to have a significant association with a decreased risk of colorectal cancer in homozygous model ( = 0.006) and recessive model ( = 0.001), subgroup analysis also emerged a weakened correlation between rs4919510 polymorphism and an increased risk of papillary thyroid cancer in heterozygote model ( = 0.04). Furthermore, the prognosis of rs4919510 variant in cancer patients showed that rs4919510 GG genotype was significant association with poor recurrence-free survival in homozygous models ( = 0.04). The meta-analysis suggested that the microRNA-608 rs4919510 polymorphism maybe associate with a significantly decreased risk for colorectal cancer. Further investigations on larger populations are required to evaluate and confirm this relationship.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046227PMC
http://dx.doi.org/10.18632/aging.101476DOI Listing

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