Trujillo-Cáceres Silvia Juliana, Torres-Sánchez Luisa, Burguete-García Ana I, Orbe Orihuela Yaneth Citlalli, Vázquez-Salas Ruth Argelia, Álvarez-Topete Esmeralda, Gómez Rocío
Centro de Investigación en Salud Poblacional, Instituto Nacional de Salud Pública (INSP), Cuernavaca, Morelos, Mexico.
Centro de Investigación en Enfermedades Infecciosas, INSP, Cuernavaca, Morelos, Mexico.
Oncotarget. 2019 Jan 22;10(7):738-748. doi: 10.18632/oncotarget.26592.
Sexually transmitted infections and its contribution to prostate cancer (PC) development have been relevant in different populations. gene polymorphism (rs10993994) has exhibited an association both with PC as well as the susceptibility to sexually transmitted infections. Hitherto, these conditions have been not studied in Mexico yet, neither if sexually transmitted infections could modify the MSMB and PC association. Herein, socio-demographic features, sexually transmitted infections records, the reproductive backgrounds, and the genetic characterisation were analysed in 322 incident PC cases and 628 population healthy controls from Mexico City. Whole PC, early-onset PC (PC at < 60 years old), late-onset PC (≥ 60 years old), and PC aggressiveness were used to evaluate the genetic variants contribution to PC risk using unconditional logistic regression models. Overall, none associations between the allelic variants of rs10993994 polymorphisms with whole and PC aggressiveness were found. Howbeit, the TT genotype carriers presented the highest susceptibility to develop early-onset PC (OR = 2.66; 95% CI = 1.41, 5.04; = 0.03) than CC+CT carriers, both with codominant and recessive models. Although none association between whole PC and gene polymorphism was found, our results were reinforced by prior studies in European descendent populations, suggesting a contribution between rs10993994 and early-onset PC development.
性传播感染及其对前列腺癌(PC)发展的影响在不同人群中都具有相关性。基因多态性(rs10993994)已显示出与前列腺癌以及性传播感染易感性均有关联。迄今为止,墨西哥尚未对这些情况进行研究,也未研究性传播感染是否会改变MSMB与前列腺癌之间的关联。在此,对来自墨西哥城的322例新发前列腺癌病例和628名健康对照者的社会人口学特征、性传播感染记录、生殖背景以及基因特征进行了分析。使用无条件逻辑回归模型,以整体前列腺癌、早发性前列腺癌(<60岁的前列腺癌)、晚发性前列腺癌(≥60岁)以及前列腺癌侵袭性来评估基因变异对前列腺癌风险的影响。总体而言,未发现rs10993994多态性的等位基因变异与整体前列腺癌及侵袭性之间存在关联。然而,与CC + CT携带者相比,无论是共显性模型还是隐性模型,TT基因型携带者发生早发性前列腺癌的易感性最高(OR = 2.66;95% CI = 1.41, 5.04;P = 0.03)。尽管未发现整体前列腺癌与该基因多态性之间存在关联,但我们的结果得到了欧洲后裔人群先前研究的支持,表明rs10993994与早发性前列腺癌的发生之间存在关联。