Oncology Group, Gastroenterology Division, Federal University of Sao Paolo, SP, Brazil.
Mol Med Rep. 2012 Aug;6(2):395-8. doi: 10.3892/mmr.2012.926. Epub 2012 May 23.
The multidrug resistance 1 (MDR1) gene encodes P-glycoprotein, which confers resistance to antineoplastic drugs, but also affects the kinetic disposition of certain drugs and carcinogens. The C3435T polymorphism of the MDR1 gene may influence the transport and excretion of carcinogens, increasing the risk of cancer. The aim of this study was to evaluate the association between this polymorphism and the risk of gastric cancer (GC). Ninety-eight patients with non-cardia GC and 203 healthy subjects participated in the study. DNA was extracted from leukocytes and the MDR1 polymorphism was analyzed using PCR-RFLP. Serology was performed by ELISA for the investigation of infection with Helicobacter pylori. No significant difference in the genotype (p=0.668) or allele (p=0.745) frequency of the C3435T polymorphism was observed between the GC and control groups. There was no association between the genotypes studied and the risk of GC in patients infected with H. pylori (p=0.662). Patient survival was not correlated with the genotypes studied (p=0.454). No correlation was observed between the C3435T polymorphism of the MDR1 gene and GC risk or prognosis in the population studied.
多药耐药基因 1(MDR1)编码 P-糖蛋白,它赋予了抗药性,同时也影响了某些药物和致癌物的动力学分布。MDR1 基因的 C3435T 多态性可能会影响致癌物的转运和排泄,增加癌症的风险。本研究旨在评估这种多态性与胃癌(GC)风险之间的关联。98 例非贲门 GC 患者和 203 例健康对照者参与了研究。从白细胞中提取 DNA,并通过 PCR-RFLP 分析 MDR1 多态性。采用 ELISA 法进行血清学检测以调查幽门螺杆菌感染。GC 组和对照组之间在基因型(p=0.668)或等位基因(p=0.745)频率上均无显著差异。在感染幽门螺杆菌的患者中,研究的基因型与 GC 风险之间没有关联(p=0.662)。患者的生存与所研究的基因型无关(p=0.454)。在研究人群中,MDR1 基因的 C3435T 多态性与 GC 风险或预后之间没有相关性。