Ren Hong-Tao, Li Yi-Ming, Wang Xi-Jing, Kang Hua-Feng, Jin Tian-Bo, Ma Xiao-Bin, Liu Xing-Han, Wang Meng, Liu Kang, Xu Peng, Yao Qing-Ling, Dai Zhi-Jun
From the Departments of Oncology (H-TR, X-JW, H-FK, X-BM, X-HL, MW, KL, PX, Q-LY, Z-JD) and General Surgery (Y-ML), The Second Affiliated Hospital of Xi'an Jiaotong University; and National Engineering Research Center for Miniaturized Detection Systems, School of Life Sciences, Northwest University, Xi'an, China (T-BJ).
Medicine (Baltimore). 2016 May;95(21):e3760. doi: 10.1097/MD.0000000000003760.
Programmed death-1 (PD-1) is crucial in cancer and is well characterized as a negative T-cell regulator that functions by delivering inhibitory signals. We aimed to evaluate the relationship between PD-1 polymorphisms (rs10204525, rs2227982, and rs7421861) and breast cancer risk.We selected 560 breast cancer patients and 583 age-, sex-, and ethnicity-matched healthy controls from Northwest China. The PD-1 polymorphisms were genotyped by using Sequenom MassARRAY. Associations were estimated with odds ratios (ORs) and 95% confidence intervals (95% CIs).For the rs10204525 and rs7421861 polymorphisms, no differences in breast cancer risk were found in any of the genetic models. For the rs2227982 polymorphism, the variant genotypes were significantly associated with decreased breast cancer risk (CT vs CC: OR = 0.68, 95% CI = 0.52-0.91; CT + TT vs CC: OR = 0.69, 95% CI = 0.53-0.90). In analyses stratified by age, the decreased risk was observed among the younger subjects (OR = 0.68, 95% CI = 0.47-0.97). We found that the decreased risk observed for the variant genotypes of rs2227982 was associated with the Her-2 status (CT vs CC: OR = 0.55, 95% CI = 0.37-0.84; CT + TT vs CC: OR = 0.56, 95% CI = 0.38-0.82). The haplotype analysis showed that the Ars10204525 Trs2227982 Crs7421861 haplotype was associated with a significantly decreased risk of breast cancer (OR = 0.50, 95% CI = 0.34-0.75).Our findings support an association between the PD-1 rs2227982 polymorphism and decreased breast cancer risk, especially in Her-2 positive breast cancer patients in the Chinese population.
程序性死亡蛋白1(PD-1)在癌症中起着关键作用,它作为一种负性T细胞调节因子,通过传递抑制性信号发挥作用,这一点已得到充分阐明。我们旨在评估PD-1基因多态性(rs10204525、rs2227982和rs7421861)与乳腺癌风险之间的关系。我们从中国西北部选取了560例乳腺癌患者以及583例年龄、性别和种族相匹配的健康对照。采用Sequenom MassARRAY对PD-1基因多态性进行基因分型。通过比值比(OR)和95%置信区间(95%CI)评估相关性。对于rs10204525和rs7421861基因多态性,在任何遗传模型中均未发现乳腺癌风险存在差异。对于rs2227982基因多态性,变异基因型与乳腺癌风险降低显著相关(CT与CC相比:OR = 0.68,95%CI = 0.52 - 0.91;CT + TT与CC相比:OR = 0.69,95%CI = 0.53 - 0.90)。在按年龄分层的分析中,较年轻受试者中观察到风险降低(OR = 0.68,95%CI = 0.47 - 0.97)。我们发现,rs2227982变异基因型观察到的风险降低与Her-2状态相关(CT与CC相比:OR = 0.