Department of Medical Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang - China.
Int J Biol Markers. 2009 Oct-Dec;24(4):230-7. doi: 10.1177/172460080902400403.
The development of resistance to chemotherapy is one of the major obstacles in the treatment of non-small cell lung cancer (NSCLC). The purpose of this study was to investigate the prognostic value of multidrug resistance protein 1 (MRP1), breast cancer resistance protein (BCRP), lung resistance-related protein (LRP), and excision repair cross-complementing 1 (ERCC1) in NSCLC patients receiving cisplatin-based adjuvant chemotherapy (cisplatin plus vinorelbine or gemcitabine) after tumor resection. We used semiquantitative reverse-transcription polymerase chain reaction to detect the expression of MRP1, BCRP, LRP and ERCC1 mRNA in surgical resection specimens of 60 patients with stage IB through IIIA NSCLC. The expression level of each gene was analyzed in relation to clinicopathological factors, tumor-free survival (TFS), and overall survival. The results showed that stage IIIA (p=0.011), N1 and N2 status (p=0.008), high expression of MRP1 (p=0.034) and LRP (p=0.018) were associated with shorter TFS. Stage IIIA (p=0.0105), N1 and N2 status (p=0.009), high expression of MRP1 (p=0.021) and ERCC1 (p=0.012) were related to a shorter overall survival. Cox multivariate analyses revealed that early stage (p=0.013 and p=0.024), negative lymph node status (p=0.006 and p=0.011), and low MRP1 expression (p=0.022 and p=0.035) were independent predictors of favorable TFS and overall survival, respectively. Additionally, ERCC1 (p=0.019) was an independent predictor of favorable overall survival.
化疗耐药的发展是治疗非小细胞肺癌(NSCLC)的主要障碍之一。本研究旨在探讨多药耐药蛋白 1(MRP1)、乳腺癌耐药蛋白(BCRP)、肺耐药相关蛋白(LRP)和切除修复交叉互补基因 1(ERCC1)在接受顺铂为基础的辅助化疗(顺铂联合长春瑞滨或吉西他滨)的 NSCLC 患者中的预后价值。我们使用半定量逆转录聚合酶链反应检测 60 例 IB 期至 IIIA 期 NSCLC 患者手术切除标本中 MRP1、BCRP、LRP 和 ERCC1 mRNA 的表达。分析每个基因的表达水平与临床病理因素、无病生存期(TFS)和总生存期的关系。结果显示,III 期(p=0.011)、N1 和 N2 状态(p=0.008)、MRP1(p=0.034)和 LRP(p=0.018)高表达与较短的 TFS 相关。III 期(p=0.0105)、N1 和 N2 状态(p=0.009)、MRP1(p=0.021)和 ERCC1(p=0.012)高表达与较短的总生存期相关。Cox 多因素分析显示,早期(p=0.013 和 p=0.024)、阴性淋巴结状态(p=0.006 和 p=0.011)和低 MRP1 表达(p=0.022 和 p=0.035)是 TFS 和总生存期的独立预后因素。此外,ERCC1(p=0.019)是总生存期的独立预后因素。