Genetic Variation of TGF-ΒR2 As a Protective Genotype for the Development of Colorectal Cancer in Men.

BACKGROUND The role of transforming growth factor beta (TGF-beta) signaling, including both the cytokine and their receptors, in the etiology of colorectal cancer (CRC) has been of particular interest lately. AIM To investigate the association between promoter polymorphism in TGF-beta receptor 2 TGF-& UBeta;R2G([-875])A with a CRC risk in a cohort of Bulgarian patients using a case-control gene association study approach, as well as the protein levels of TGF-beta 1 in the peripheral blood. METHODS A cohort of 184 CRC patients and 307 sex and age-matched healthy subjects were recruited in the study. A genotyping of the TGF-& UBeta;R2G([-875])A (rs3087465) polymorphism was performed by primer-introduced restriction analyses-polymerase chain reaction approaches. RESULTS The frequency of TGF-& UBeta;R2G([-875])A genotype was decreased in male patients with CRC than in healthy men (31.3% vs 44.8%; P = 0.058). Among males, the TGF-& UBeta;R2G([-509])G genotype was related to a significantly increased risk of CRC development (OR = 1.820, 95%CI: 0.985-3.362, P = 0.055) than the GA + AA genotype. Also, TGF-& UBeta;R2([-875])*A-allele itself was rarer in men with CRC than healthy men (19.1% vs 26.9%, P = 0.086) and was associated with a protective effect (OR = 0.644; 95%CI: 0.389-1.066; P = 0.086). Regarding the genotypes, we found that TGF-beta 1 serum levels were higher in GG genotype in healthy persons above 50 years than the CRC patients [36.3 ng/mL interquartile range (IQR) 19.9-56.5 vs 22.4 ng/mL IQR 14.8-29.7, P = 0.014]. We found significant differences between higher levels of TGF-beta 1 serum levels in healthy controls above 50 years (GG genotype) and CRC patients (GG genotype) at the early stage (36.3 ng/mL IQR 19.9-56.5 vs 22.8 ng/mL IQR 14.6-28.6, P = 0.037) and advanced CRC (36.3 ng/mL IQR 19.9-56.5 vs 21.6 ng/mL IQR 15.9-33.9, P = 0.039). CONCLUSION In summary, our results demonstrated that TGF-& UBeta;R2 AG and AA genotypes were associated with a reduced risk of CRC, as well as circulating levels of TGF-beta could prevent CRC development in a gender-specific manner. Notably, male carriers of TGF-& UBeta;R2 -875A allele genotypes had a lower risk of CRC development and progression, suggesting that TGF-& UBeta;R2 -875A/G polymorphism significantly affects the protective biological factors that also impact the risk of colon and rectal carcinogenesis.