Huang Zhao-Hui, Hua Dong, Li Li-Hua
Wuxi Oncology Institute, The Fourth Affiliated Hospital of Suzhou University, 200 Huihe Road, 214062, Wuxi, Jiangsu Province, China.
Cancer Chemother Pharmacol. 2009 Apr;63(5):911-8. doi: 10.1007/s00280-008-0815-6. Epub 2008 Aug 15.
The aim of this study was to investigate the association of the thymidylate synthase (TS) and methylenetetrahydrofolate reductase (MTHFR) polymorphisms with the clinical outcomes of gastric cancer patients treated with 5-FU-based adjuvant chemotherapy.
One-hundred and sixteen patients with gastric cancer were treated with 5-FU-based adjuvant chemotherapy. The TS (a 28-bp tandem repeat polymorphism in the TS enhancer region (TSER) and a 6 bp deletion/insertion polymorphism in the 3'-untranslated region) and MTHFR C677T polymorphisms were determined in blood samples from those patients using PCR and PCR-LDR (ligation detection reaction) method, respectively.
The overall survival (OS) in patients with the TS ins6/ins6 genotype was significantly shorter than those in patients with the del6/del6 (P = 0.017) and ins6/del6 (P = 0.022) genotype. The relapse-free survival (RFS) and OS in patients with the MTHFR C/C genotype were significantly worse than those in patients with the T/T or C/T genotype (P = 0.043 and 0.040, respectively). Cox multivariate analysis also showed that patients with the TS ins6/ins6 genotype have worse OS than patients with the T/T or C/T genotype (HR = 2.437, P = 0.041), and the MTHFR C/C genotype was associated with shorter RFS (HR = 1.723, P = 0.031) and OS (HR = 1.681, P = 0.056). No significant association was found between the TSER polymorphism and the clinical outcomes (P > 0.05).
The polymorphisms of TS 3'-UTR ins6/del6 and MTHFR C677T appear to be potential prognostic factors in gastric cancer patients treated with 5-FU-based adjuvant chemotherapy, which may allow identification of gastric cancer patients who will benefit from 5-FU chemotherapy.
本研究旨在探讨胸苷酸合成酶(TS)和亚甲基四氢叶酸还原酶(MTHFR)基因多态性与接受基于5-氟尿嘧啶(5-FU)辅助化疗的胃癌患者临床结局之间的关联。
116例胃癌患者接受了基于5-FU的辅助化疗。分别采用聚合酶链反应(PCR)和PCR-连接检测反应(LDR)方法,检测这些患者血液样本中TS(TS增强子区域(TSER)的28 bp串联重复多态性和3'-非翻译区的6 bp缺失/插入多态性)和MTHFR C677T基因多态性。
TS基因ins6/ins6基因型患者的总生存期(OS)显著短于del6/del6基因型(P = 0.017)和ins6/del6基因型(P = 0.022)患者。MTHFR C/C基因型患者的无复发生存期(RFS)和OS显著差于T/T或C/T基因型患者(分别为P = 0.043和0.040)。Cox多因素分析还显示,TS基因ins6/ins6基因型患者的OS比T/T或C/T基因型患者差(风险比(HR)= 2.437,P = 0.041),MTHFR C/C基因型与较短的RFS(HR = 1.723,P = 0.031)和OS(HR = 1.681,P = 0.056)相关。未发现TSER多态性与临床结局之间存在显著关联(P > 0.05)。
TS基因3'-UTR ins6/del6和MTHFR C677T多态性似乎是接受基于5-FU辅助化疗的胃癌患者潜在的预后因素,这可能有助于识别将从5-FU化疗中获益的胃癌患者。