AI Article Synopsis

  • The study investigates the role of MMP-7 gene variants in the risk of hepatocellular carcinoma (HCC) in Taiwan, where HCC rates are particularly high.
  • Researchers compared MMP-7 genotypes in 298 HCC patients and 889 healthy individuals, analyzing lifestyle factors like smoking and drinking.
  • Findings showed no significant link between MMP-7 variants and HCC risk, suggesting these genotypes are not reliable markers for the disease in the Taiwanese population.

Article Abstract

Background/aim: Metalloproteinase-7 (MMP-7) has been previously found to be up-regulated in hepatocellular carcinoma (HCC) specimens and cells, favoring epithelial-mesenchymal transition. However, the contribution of MMP-7 genotypes to HCC has not been revealed to date. The study aimed to evaluate the contribution of MMP-7 promoter A-181G (rs11568818) and C-153T (rs11568819) genotypes on the risk of HCC in Taiwan, where HCC incidence is extremely high compared to worldwide data.

Materials And Methods: In this case-control study, MMP-7 genotypes and their association with cigarette smoking and alcohol drinking habits were determined in 298 HCC patients and 889 healthy subjects by a typical polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methodology.

Results: Ever smokers and alcohol drinkers were represented with higher percentages in the case group compared to the control group. MMP-7 rs11568818 genotypes were not found differentially distributed in case and control groups (p for trend=0.5246). People of the analyzed cohort of the present study were all of CC genotypes at their rs11568819 polymorphic sites, without any CT or TT genotypes. As for gene-lifestyle interactions, people with variant genotypes at MMP-7 rs11568818 had the same odds for HCC development compared to the wild-type AA genotype, no matter whether the subjects belonged to the smoker, non-smoker alcohol drinker, or non-drinker groups.

Conclusion: MMP-7 variant genotypes did not present any significance towards being a marker for HCC risk in Taiwanese.

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Source
http://dx.doi.org/10.21873/anticanres.16034DOI Listing

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