非小细胞肺癌组织中ERCC1和RRM1表达与抗肿瘤治疗的疗效及预后关系

李竟长, 倪秉强, 陈日新, 朱州

李竟长, 倪秉强, 陈日新, 朱州. 非小细胞肺癌组织中ERCC1和RRM1表达与抗肿瘤治疗的疗效及预后关系[J]. 实用临床医药杂志, 2013, (1): 21-23. DOI: 10.7619/jcmp.201301006
引用本文: 李竟长, 倪秉强, 陈日新, 朱州. 非小细胞肺癌组织中ERCC1和RRM1表达与抗肿瘤治疗的疗效及预后关系[J]. 实用临床医药杂志, 2013, (1): 21-23. DOI: 10.7619/jcmp.201301006
LI Jingzhang, NI Bingqiang, CHEN Rixin, ZHU Zhou. Expression of excision repair cross complementing gene1 and ribonucleotide reductase M1 in non-small cell lung cancer tissue and therapeutic effects of trecombinant human endostatin combined with gemcitabine/cisplatin and its prognostic relationship[J]. Journal of Clinical Medicine in Practice, 2013, (1): 21-23. DOI: 10.7619/jcmp.201301006
Citation: LI Jingzhang, NI Bingqiang, CHEN Rixin, ZHU Zhou. Expression of excision repair cross complementing gene1 and ribonucleotide reductase M1 in non-small cell lung cancer tissue and therapeutic effects of trecombinant human endostatin combined with gemcitabine/cisplatin and its prognostic relationship[J]. Journal of Clinical Medicine in Practice, 2013, (1): 21-23. DOI: 10.7619/jcmp.201301006

非小细胞肺癌组织中ERCC1和RRM1表达与抗肿瘤治疗的疗效及预后关系

基金项目: 中国高校医学期刊临床专项资金
详细信息
  • 中图分类号: R734.2

Expression of excision repair cross complementing gene1 and ribonucleotide reductase M1 in non-small cell lung cancer tissue and therapeutic effects of trecombinant human endostatin combined with gemcitabine/cisplatin and its prognostic relationship

  • 摘要: 目的 探讨核苷酸还原酶亚单位M1 (RRM1)和核苷酸切除修复交叉互补基因1(ERCC1)蛋白在ⅢB和Ⅳ期非小细胞肺癌(NSCLC)中的表达,及其对重组人血管内皮抑制素(恩度)联合吉西他滨/奈达铂化疗疗效的预测.方法 采用免疫组织化学方法检测51例ⅢB~Ⅳ期肺癌患者组织中ERCC1和RRM1的表达水平.经过4周期以上恩度联合吉西他滨/奈达铂方案化疗,分析比较不同ERCC1和RRM1表达水平与NSCLC治疗预后的关系.结果 NSCLC组织中ERCC1的阳性率为43.1%,RRM1的阳性率为62.7%.RRM1与ERCC1蛋白表达显著正相关.RRM1和ERCC1表达均为阴性组的有效率为72.2%;二者表达均为阳性组为19.0%;二者表达任一阳性组为58.3%,3组之间比较差异均有统计学意义;ERCC1和RRM1低表达的患者生存期明显长于高表达者.结论 ERCC1和RRM1的表达可作为NSCLC患者恩度联合吉西他滨/奈达铂方案化疗敏感性及其预后判断的指标之一.
  • Olaussen K A, Dunant A, Fouret P. DNA repair by ERCC1 in non small cell lung cancer and cisplatin-based adjuvant chemotherapy [J]. N Earl J Med, 2006, (10):983.
    Martin L P, Hamilton T C, Schilder R J. Platinum resistance:the role of DNA repair pathways [J]. Clinical Cancer Research, 2008(5):1291.
    程刚. 非小细胞肺癌"个体化"化疗研究进展 [J]. 中国肺癌杂志, 2008(1):10.
    Seetharam R N, Sood A, Basu-mallick A. Oxaliplatin No sistance induced by ERCC1 up-regulation is abrogated by siRNA mediated gene silencing in human colorectal cancer cells [J]. Anticancer Research, 2010(7):2531.
    Kirschner K, Melton D W. Multiple roles of the ERCC1XPF endonuclease in DNA repair and resistance to anticancer drags [J]. Anticancer Research, 2010(9):3223.
    Kim S O, Jeong J Y, Kim M R. Efficacy of gmeitabine in ptients with non-small cell lung cancer according to promoter polymorphisms of the ribonueleotide reducume Mi gene [J]. Clinical Cancer Research, 2008, (10):3083.
    Croteau D L, Peng Y, Van Houten B. DNA repair gets physical:mapping an XPA-binding site on ERCC1 [J]. DNA Repair (Amat), 2008(5):819.
    Pan J, Lin J, Izzo J G. Genetic susceptibility to esophageal cancer:the role of the nueleotide excision repair pathway [J]. Carcinogenesis, 2009(5):785.
    Reynolds C, Obasaju C, Schell M J. Randomized phase Ⅲ trial of gemcitabine-based chemotherapy with in situ RRM1 and ERCC1 protein levels for response prediction in Non small cell lung cancer [J]. Journal of Clinical Oncology, 2009, (34):5808.
    Itssaka S, Komaki R, Herbst R S. Endostatin improves radioresponse and blocks tumor revascuhrization after radiation therapy for A431 xenografis in mice [J]. International Journal of Radiation Oncology, Biology, Physics, 2007(3):870.
计量
  • 文章访问数:  317
  • HTML全文浏览量:  31
  • PDF下载量:  13
  • 被引次数: 0
出版历程
  • 发布日期:  2013-05-01

目录

    /

    返回文章
    返回
    x 关闭 永久关闭