期刊文献+

晚期非小细胞肺癌HIF-1α、ERCC1基因多态性与铂类药物疗效的关系 被引量:16

Correlation among HIF-1α,ERCC1 genetic polymorphisms and outcome of NSCLC patients receiving platinum-based chemotherapy
下载PDF
导出
摘要 目的:探讨HIF-1α和ERCC1基因多态性与铂类药物对NSCLC疗效的相关性。方法:选取我院采用铂类药物治疗的晚期NSCLC患者,经PCR-RFLP方法检查患者HIF-1α基因C1772T和ERCC1基因C118T基因型,分析不同基因型之间化疗疗效的差异。结果:患者HIF-1α基因C1772T和ERCC1基因C118T两个多态位点均符合Hardy-Weinberg遗传平衡规律;携带HIF-1αCT+TT基因型患者的铂类药物治疗有效率显著高于CC型;携带ERCC1 CC基因型患者的铂类药物治疗有效率显著高于CT+TT型。102例患者中有4例失访,98例患者中位TTP为7.0个月,携带HIF-1αCT+TT基因型患者中位TTP为7.0个月,而CC基因型为6.0个月,差异无统计学意义;携带ERCC1 CC基因型患者的中位TTP为7.0个月,而CT+TT基因型为6.0个月,差异无统计学意义。结论 :HIF-1α基因的CT+TT基因型和ERCC1的CC基因型患者的铂类药物化疗有效率高,并且ERCC1的CC基因型患者的预后更好。 Objective To analyze the relationship among HIF-1α, ERCC1 gene polymorphisms and the effects of platinum-based chemotherapy for the treatment of advanced non-small cell lung cancer (NSCLC) Methods HIF-1α C1772T and ERCC1 CIlST loci were genotyped with PCR-RFLP method. The relationship between genotypes and the outcome of treatment as well as TIP was investigated. Results HIF-1α and ERCC1 of 102 patients were under the Hardy-Weinberg equilibrium. Patients with HIF-1α CT+TT genotype showed a significantly higher chemotherapeutic efficiency compared with patients with CC genotype; Patients with ERCC1 CC genotype showed a significantly higher chemotherapeutic efficiency compared with patients with CT +TT genotype. The median TIP was 7.0 months for the 98 patients followed-up; 7.0 months for HIF-1α CT+TT genotype, and 6.0 months for CC genotype, and the difference showed no significance; The median TIP was 7.0 months for ERCC1 CC genotype, and 6.0 months for CT+TT genotype, and the difference was statistically significant. Conclusions Patients with HIF-1α CT+TT genotype or ERCC1 CC genotype have showed higher chemotherapeutic efficiency, and patients with ERCC1 CC genotype show longer median TIP.
出处 《实用医学杂志》 CAS 北大核心 2016年第3期385-388,共4页 The Journal of Practical Medicine
基金 连云港市卫生局科研项目(编号:1224)
关键词 非小细胞肺 多态性 Non-small cell carcinoma Platinum Gene polymorphism
  • 相关文献

二级参考文献9

  • 1Cobo M, Isla D, Massuti B, et al. Customizing Cisplatin based on quantitative excision repair cross-complementing 1 mRNA expression: A phase m trial in non-small-cell lung cancer [J]. J Clin Oneol, 2007,25(19) :2747-2754.
  • 2Olaussen KA, Dunant A, Fouret P, et al. DNA repair by ERCC1 in non-small cell lung cancer and Cisplatin-basedadjuvant chemotherapy[J]. N Engl J Med, 2006,355 (10):983- 991.
  • 3Reynolds C, Obasaju C, Schell M J, et al. Randomized phase m trial of Gemcitabine-based chemotherapy with in situ RRM1 and ERCC1 protein levels for response prediction in non-small cell lung cancer [J]. J Clin Oncol,2009,27(34) :5808-5815.
  • 4Taron M, Rosell R, Felip E, et al. BRCA1 mRNA expression levels as an indicator of ehemo-resistanee in lung cancer [J]. Hum Mol Genetic, 2004, 13:2443-2449.
  • 5Wu J, Liu J, Zhou Y, et al. Predictive value of XRCC1 gene polymorphisms on platinum-based chemotherapy in advanced non-small cell lung cancer patients: A systematic review and meta-analysis[J]. Clin Cancer Res, 2012,18:3972-3981.
  • 6Zhang ZY, Tian X, Wu R, et al. Predictive role of ERCC1 and XPD genetic polymorphisms in survival of Chinese non-small cell lung cancer patients receiving chemotherapy[J]. Asian Pac J Cancer Prev, 2012,13(6) :2583-2586.
  • 7Boni C, Tiseo M, Boni L, et al. Triplets versus doublets, with or without Cisplatin, in the first-line treatment of stage m B-rV non-small cell lung cancer (NSCLC) patients: A muhicenter randomized factorial trial (FAST)[J]. Br J Cancer 2012,106 (4) : 658-665.
  • 8Bepler G, Williams CC, Schell ML, et al. Molecular analysis- directed, international, phase HI trial in patients with advanced non-small-cell lung cancer[J]. J Clin Oncol, 2013,31 (15s): abstr 8001.
  • 9Moran T, Cobo M, Domine M, et al. Interim analysis of The Spanish Lung Cancer Group (SLCG) BRCA1-RAP80 Expression Customization (BREC) randomized phase 11I trial of customized therapy in advanced non-small-cell lung cancer (NSCLC) patients (p) (NCT00617656/GECP-BREC)[J]. J Clin Oncol, 2013,31 (18s) : Abstr LBA8002.

共引文献19

同被引文献175

  • 1杨学宁,吴一龙.实体瘤治疗疗效评价标准——RECIST[J].循证医学,2004,4(2):85-90. 被引量:1520
  • 2郑树,黄彦钦.NCCN结肠癌临床诊疗指南解读[J].实用肿瘤杂志,2007,22(3):206-207. 被引量:35
  • 3H Yi D, Appel S. Current status and future perspectives of dendritic cell- based cancer immunotherapy[J].Scand J Immunol, 2013, 78(2): 167-171.
  • 4Zheng YW, Li RM, Zhang XW, et al. Current adoptive immunotherapy in non-small cell lung cancer and potential influence of therapy outcome[J]. Cancer Invest, 2013, 31 ( 3 ) : 197-205.
  • 5DERMAN BA, MILEHAM KF, BONOMI PD, et al. Treatment of advanced squamous Cell carcinoma of the lung: a review[J]. Transl Lung Cancer Res, 2015,4 (5) : 524-532.
  • 6STEFAN A, TILMAN T, GEORGIOS G, et al. Thymidine kinase and cancer monitoring [J]. Cancer Letters, 2012,316 (1):6-10.
  • 7SHARIF H, VON EULER H, WESTBERQ S, et al. A sensitive and kinetically defined radiochemical assay for canine and human serum thymidine kinase 1 (TK1) to monitor canine malignant lymphoma [J]. Vet J, 2012,194( 1 ) : 40-47.
  • 8WU B J, L! W, QIAN C, et al. Increased serum level of thymidine kinase 1 correlates with metastatic site in patients with malignant melanoma [J]. Tumor Biol, 2013, 34(2) :643-648.
  • 9BOLAYIRLI M, PAPILA C, KORKMAZ GG, et al. Serum thymidine kinase 1 activity in solid tumor (breast and eoloreetal cancer) patients treated with adjuvant chemotherapy [J]. J Clin Lab Anal, 2013,27(3) :220-226.
  • 10SIEGEL RL, MILER KD, JEMAL A. Cancer Statistics, 2015 [J]. CA CANCER J CIAN, 2015,65:5-29.

引证文献16

二级引证文献89

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部