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DOI 10.5301/jbm.5000079

Медицинская библиотека · The International journal of biological markers · 2014

Resistin -420C>G promoter variant and colorectal cancer risk.

Mahmoudi Touraj, Karimi Khatoon, Arkani Maral, Farahani Hamid, Vahedi Mohsen, Dabiri Reza, Nobakht Hossein, Asadi Asadollah, Mirakhorli Mojgan, Arshi Benafsheh, Derakhshan Arash, Zali Mohammad Reza

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

PURPOSES: Obesity is associated with an increased risk of colorectal cancer (CRC), and ghrelin (GHRL) and resistin (RETN) are thought to be related to obesity. Our aim was to investigate whether GHRL and RETN gene variants are associated with CRC risk.

MATERIALS AND

METHODS

All 414 subjects, including 197 cases with CRC and 217 controls, were genotyped for the GHRL (rs26802) and RETN (rs1862513) or -420 C>G gene variants using the PCR-RFLP method.

RESULTS

Our findings indicated that the RETN -420 C>G "CC" genotype, compared with the "GG" and "GC" genotypes, was a marker of decreased CRC susceptibility; the difference remained significant after adjustment for age, BMI, gender, smoking status, NSAID use, and family history of CRC (p=0.020; OR=0.52, 95% CI=0.30-0.90). Furthermore, after adjustment for confounding factors, the -420 C>G "CC" genotype, compared with the "GG" genotype, was associated with a decreased risk for CRC (p=0.044; OR=0.53, 95% CI=0.29-0.98). In addition, no significant difference was observed for the GHRL (rs26802) gene variant.

CONCLUSIONS

To our knowledge, this is the first study suggesting that the RETN -420 C>G "CC" genotype is a marker of decreased CRC susceptibility. This observation is relevant from a scientific perspective and deserves further investigations.

Для цитирования: Mahmoudi Touraj, Karimi Khatoon, Arkani Maral, Farahani Hamid, Vahedi Mohsen, Dabiri Reza, Nobakht Hossein, Asadi Asadollah, Mirakhorli Mojgan, Arshi Benafsheh, Derakhshan Arash, Zali Mohammad Reza. Resistin -420C>G promoter variant and colorectal cancer risk.. The International journal of biological markers. 2014. DOI: 10.5301/jbm.5000079.

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