Relationship between Glutathione S-Transferase P1 (GSTP1), X-Ray Repair Cross Complementing Group 1 (XRCC1) and 5,10-Methylenetetrahydrofolate Reductase (5,10-MTHFR) Gene Polymorphisms and Response to Chemotherapy in Advanced Gastric Cancer

Relationship between Glutathione S-Transferase P1 (GSTP1), X-Ray Repair Cross Complementing Group 1 (XRCC1) and 5,10-Methylenetetrahydrofolate Reductase (5,10-MTHFR) Gene Polymorphisms and Response to Chemotherapy in Advanced Gastric Cancer
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谷胱甘肽 S-转移酶 P1 (GSTP1)、X 射线修复交叉互补组 1 (XRCC1) 和 5,10-亚甲基四氢叶酸还原酶 (5,10-MTHFR) 基因多态性与晚期胃癌化疗反应的关系

DOI:
10.1159/000351260
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发表时间:
2013-06-01
期刊:
影响因子:
0.3
通讯作者:
Wu, Chang-Ping
Wu, Chang-Ping
中科院分区:
其他
文献类型:
--
作者:
Ji, Mei;Xu, Bin;Wu, Chang-Ping

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背景:本研究旨在探讨谷胱甘肽S-转移酶P1(GSTP1)、5,10-亚甲基四氢叶酸还原酶(5,10-MTHFR)和X射线修复交叉互补组1(XRCC1)基因多态性与晚期胃癌化疗反应的关系。患者和方法:纳入59例晚期胃癌患者。所有患者均接受包含多西紫杉醇、顺铂和 5-氟尿嘧啶的 DCF 方案治疗。通过聚合酶链反应/连接酶检测反应(PCR-LDR)分析所有患者的 GSTP1、XRCC1 和 5,10-MTHFR 基因型。结果:GSTP1 中 G/G 基因型 15 例(25.42%),G/A 基因型 21 例(35.59%),A/A 基因型 23 例(38.98%),A/A 基因型 16 例(27.12%),G/A 基因型 18 例(30.51%),25 例。 XRCC1 为 G/G 基因型(42.37%),5,10-MTHFR 为 C/C 基因型 21 例(35.59%),C/T 基因型 22 例(37.29%),T/T 基因型 16 例(27.12%)。化疗2个周期后,完全缓解4例,部分缓解14例,病情稳定19例,疾病进展22例,总有效率30.51%。 GSTP1 G/G 基因型、XRCC1 A/A 基因型和 5,10-MTHFR T/T 基因型的存活率更高 (p < 0.05)。结论:GSTP1 G/G、XRCC1 A/A、5,10-MTHFR T/T基因多态性对预测晚期胃癌DCF方案疗效具有临床价值。
Background: Our study aimed to investigate the relationship between glutathione S-transferase P1 (GSTP1), 5,10-methylenetetrahydrofolate reductase (5,10-MTHFR) and X-ray repair cross complementing group 1 (XRCC1) gene polymorphisms and the response to chemotherapy in advanced gastric cancer. Patients and Methods: 59 cases of advanced gastric cancer were enrolled. All patients were treated with the DCF regimen comprising docetaxel, cisplatin, and 5-fluorouracil. All patients' genotypes regarding GSTP1, XRCC1, and 5,10-MTHFR were analyzed by polymerase chain reaction/ligase detection reaction (PCR-LDR). Results: There were 15 (25.42%) cases of G/G genotype, 21 (35.59%) of G/A genotype, and 23 (38.98%) of A/A genotype for GSTP1, 16 (27.12%) cases of A/A genotype, 18 (30.51%) of G/A genotype, and 25 (42.37%) of G/G genotype for XRCC1, and 21 (35.59%) cases of C/C genotype, 22 (37.29%) of C/T genotype, and 16 (27.12%) of T/T genotype for 5,10-MTHFR. After 2 cycles of chemotherapy, there were 4 cases of complete remission, 14 of partial remission, 19 of stable disease, and 22 of advanced disease, with a total effective rate of 30.51%. Better survival was shown for GSTP1 G/G genotype, XRCC1 A/A genotype, and 5,10-MTHFR T/T genotype (p < 0.05). Conclusion: The gene polymorphisms of GSTP1 G/G, XRCC1 A/A, and 5,10-MTHFR T/T have clinical value for predicting the response to the DCF regimen for advanced gastric cancer.