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首页> 外文期刊>Pharmacogenetics and genomics >Thymidylate synthase haplotype is associated with tumor recurrence in stage II and stage III colon cancer.
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Thymidylate synthase haplotype is associated with tumor recurrence in stage II and stage III colon cancer.

机译:胸苷酸合酶单倍型与II期和III期结肠癌的肿瘤复发相关。

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摘要

BACKGROUND: Tumor recurrence after curative resection is a major problem in the management of colon cancer therapy. Identifying molecular markers for tumor recurrence is critical for successfully selecting patients who are more likely to benefit from adjuvant chemotherapy. We analyzed the value of thymidylate synthase (TS) and methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms as a prognostic marker in stage II and stage III colon cancer patients treated with 5-fluorouracil-based adjuvant chemotherapy. METHODS: Between 1987 and 2007, blood samples were obtained from 197 patients with stage II or stage III colon cancer at medical facilities at the University of Southern California. DNA was extracted from peripheral blood, and the genotypes were analyzed using PCR-restriction fragment length polymorphism technique. RESULTS: Patients harboring the TS 3RG/+6-bp haplotype were at greatest risk to develop tumor recurrence [relative risk (RR): 2.25; 95% confidence interval (CI): 1.04-4.85; adjusted P value=0.032]. TS enhancer region 3RG alone (RR: 3.48 years; 95% CI: 1.61-7.54; adjusted P value=0.013) or in combination with TS 1494del6 bp (RR: 3.41 years; 95% CI: 1.33-8.75; adjusted P value=0.044) proved to be adverse prognostic markers in both univariate and multivariable analysis. CONCLUSION: 'High-expression' variants of TS 2R/3R repeat, TS enhancer region 3R G/C, TS 1494del6 bp, and TS haplotype analysis might help to identify stage II and stage III colon cancer patients who are at great risk of developing tumor recurrence, and also those who are more likely to benefit from 5-fluorouracil-based adjuvant chemotherapy. Larger, independent, prospective studies are, however, needed to confirm and validate our preliminary findings.
机译:背景:根治性切除术后的肿瘤复发是结肠癌治疗管理中的一个主要问题。鉴定肿瘤复发的分子标志物对于成功选择更可能受益于辅助化疗的患者至关重要。我们分析了胸苷酸合酶(TS)和亚甲基四氢叶酸还原酶(MTHFR)基因多态性作为基于5-氟尿嘧啶辅助化疗治疗的II期和III期结肠癌患者的预后指标的价值。方法:1987年至2007年之间,在南加州大学的医疗机构中从197例II期或III期结肠癌患者中采集了血液样本。从外周血中提取DNA,并使用PCR-限制性片段长度多态性技术分析基因型。结果:携带TS 3RG / + 6-bp单倍型的患者发生肿瘤复发的风险最高[相对风险(RR):2.25; 95%置信区间(CI):1.04-4.85;调整后的P值= 0.032]。单独使用TS增强子区域3RG(RR:3.48年; 95%CI:1.61-7.54;调整后的P值= 0.013)或与TS 1494del6 bp组合使用(RR:3.41年; 95%CI:1.33-8.75;调整后的P值= 0.044)在单变量和多变量分析中均被证明是不良的预后指标。结论:TS 2R / 3R重复序列,TS增强子区域3R G / C,TS 1494del6 bp和TS单倍型分析的“高表达”变体可能有助于鉴定II期和III期结肠癌患者,这些患者有高度的发展风险肿瘤复发,以及那些更可能受益于基于5-氟尿嘧啶的辅助化疗的患者。但是,需要更大,独立的前瞻性研究来确认和验证我们的初步发现。

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