期刊文献+

EGFR野生型NSCLC患者ERCC1、RRM1、TYMS和TUBB3 mRNA表达水平对化疗效果和预后的影响 被引量:1

Effects of mRNA expressions of ERCC1,RRM1,TYMS,and TUBB3 of NSCLC patients with wild-type EGFR on efficacy and prognosis of chemotherapy
在线阅读 下载PDF
导出
摘要 目的联合检测EGFR野生型非小细胞肺癌(NSCLC)患者的ERCC1、RRM1、TYMS和TUBB3的mRNA表达水平差异,以探究4种基因的表达水平对化疗效果及预后的影响。方法将353例NSCLC患者的标本通过xTAG-液相芯片法筛选出EGFR野生型患者,采用实时荧光定量PCR检测标本中4种基因的mRNA表达水平。EGFR野生型患者中4种基因均高表达的为高表达组,否则为低表达组,比较两组患者接受化疗后的中位无进展生存期及中位总生存期。结果遴选出EGFR野生型NSCLC患者227例,除吸烟与不吸烟者外,其他不同特征型患者之间4种基因mRNA表达水平之间差异无统计学意义(P〉0.05)。野生型高表达组有27例,野生型低表达组有53例,两组患者客观缓解率(ORR)(14.8%vs 41.5%,P〈0.05)、疾病控制率(DCR)(40.7%vs 81.1%,P〈0.05)、中位无进展生存期(月)(3.3 vs 4.9,P=0.001)与中位总生存期(月)(7.1 vs 8.1,P=0.048)间差异均有统计学意义。Cox多因素分析显示,4种基因高表达为EGFR野生型NSCLC患者化疗预后的独立危险因素(HR=1.92;95%CI:1.10~3.42)。结论 EGFR野生型NSCLC患者肿瘤组织的ERCC1、TYMS、TUBB3和RRM1 mRNA为高表达水平时,预示其对化疗药物具有耐药性。联合检测4种基因的表达有利于化疗方案的选择。 Objective To jointly detect the differences of mRNA expressions of ERCC1,RRM1,TYMS,and TUBB3 of non-small cell lung cancer(NSCLC) patients with wild type epidermal growth factor receptor(EGFR) and explore the effects of expressions of 4 genes on the efficacy and prognosis of chemotherapy.Methods Patients with wild type EGFR were screened by xTAG liquid phase chip method from samples of 353 NSCLC patients.The mRNA expression levels of 4 genes were detected by real-time PCR.Patients with wild type EGFR were divided into the high expression group(expressions of 4 genes were high) and low expression group(expressions of 4 genes were low).The median progression free survival and median overall survival of two groups were compared after chemotherapy.Results A total of 227 NSCLC patients with wild type EGFR were screened.The differences of mRNA expression levels of 4 genes of patients were not statistically significant(P〉0.05) except differences between smoking and non-smoking patients.There were 27 patients in the high expression group and 53 patients in the low expression group.The differences of the objective remission rate(ORR)(14.8%vs 41.5%,P〈0.05),disease control rate(DCR)(40.7%vs 81.1%,P 0.05),median progression free survival(3.3 m vs 4.9 m,P = 0.001),and median overall survival(7.1 m υs 8.1 m,P = 0.048) of two groups were statistically significant.Cox multivariate analysis showed that the high expression of 4 genes was independent risk factor of prognosis for NSCLC patients with wild type EGFR after chemotherapy(HR=1.92;95%CI:1.10-3.42).Conclusion High mRNA expressions of ERCC1,TYMS,TUBB3,and RRM1 in cancer tissue of NSCLC patients with wild type EGFR indicate that they are resistant to chemotherapeutic drugs.Joint detection of expressions of 4 genes is helpful for choosing chemotherapy plans.
出处 《上海交通大学学报(医学版)》 CAS CSCD 北大核心 2015年第7期1010-1014,1033,共6页 Journal of Shanghai Jiao tong University:Medical Science
基金 福州市科技计划项目(2011-S-68-2)~~
关键词 非小细胞肺癌 表皮生长因子受体 野生型 ERCC1 RRM1 TYMS TUBB3 non-small cell lung cancer epidermal growth factor receptor wild type ERCC1 RRM1 TYMS TUBB3
  • 相关文献

参考文献18

  • 1Siegel R, Ward E, Brawley O, et al. Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on prema- ture cancer deaths[J]. CA Cancer J Clin, 2011, 61(d): 212 - 236.
  • 2马峰,史晓宇,孟玮,张敬,赵丽霞,何晓华,赵峻峰.EGFR野生型晚期非小细胞肺癌的治疗进展[J].中国肺癌杂志,2014,17(7):575-580. 被引量:7
  • 3Ettinger DS, Akerley W, Borghaei H, et al. Non-small cell lung cancer, version 2. 2013[J]. J Natl Compr Canc Netw, 2013,11(6) : 645 -653.
  • 4Schiller JH, Harrington D, Belani CP, et al. Comparison of tour chemotherapy regimens for advanced non-small cell lung cancer[ J ]. N Engl J Med, 2002, 346(2): 92-98.
  • 5Reek M, Heigener DF, Mok T, et al. Management of non-small eell Lung eancer : recent developments [ J ]. Lancet, 2013, 382 (9893) : 709 -719.
  • 6孟庆雨,王述民,许世广,童向东,王阁浜,丁仁泉,张大坤.ERCC1、TYMS、RRM1、TUBB3表达与非小细胞肺癌化疗疗效的相关性和意义[J].中国肿瘤,2013,22(8):661-665. 被引量:6
  • 7Mok TS, Wu YL, Thongprasert S, et al. Gefitinib or carboplatin- paelitaxel in pulmonaoT adenoearcinoma[J]. N Engl J Med, 2009, 361(10) : 947 -957.
  • 8Rusell R, Moran T, Querah C, et al. Screening for epidermal growth faetor receptor mutations in lung cancer[J]. N Engl J Med, 2009, 361(10) : 958 -967.
  • 9Gong W, Zhang X, Wu J, et al. RRM1 expression and clinical out- come of gemcitabine-containing chemotherapy fur advanced nun- small-cell lung cancer: a meta-analysis[ J]. Lung Cancer, 2012, 75(3) : 374 -380.
  • 10Friboulet L, Olaussen K A, Pignon JP, et al. ERCC1 isoform expression and DNA repair in nun-small-cell lung cancer [J].N Engl J Med, 2013, 368(12) : 1101 -1110.

二级参考文献58

  • 1Jemal A,Bray F,Center MM,et al.Global cancer statistics[J] .CA Cancer J Clin,2011 ,61(2):69-90.
  • 2Santos ES, Blaya M, Raez LE.Gene expression profiling and non-small-cell lung cancer: Where are we now?[J].Clin Lung Cancer, 2009,10(3): 168.
  • 3Simon GR,Schell MJ,Begum M,et a1. Preliminary indica?tion of survival benefit from ERCCI and RRM I-tailored chemotherapy in patients with advanced nonsmall cell lung cancer: evidence from an individual patient analysis[J].Cancer, 201 2,118(9):2525-2531.
  • 4Papadaki C ,Sfakianaki M ,Ioannidis G.ERCC I and BRAC I mRNA expression levels in the primary tumor could predict the effectiveness of the second-line cis?platin-based chemotherapy in pretreated patients with metastatic non-small cell lung cancer[J]. J Thorac Oncol , 2012 (4):663-671.
  • 5Olaussen KA, Fouret P, Kroemer G. ERCCl-specific irn?munostaining in non-small-cell lung cancer[J]. N Engl J Med,2007,357 (15):1559-1561.
  • 6NCCN clinical practice Cuideliness in Oncology for NSCLC. V2.20 I O.
  • 7Shimizu T, Nakanishi Y,Nakagawa Y.Association between expression of thyrnidylate synthase, dihydrofolate reduc?tase, and glyci namide ribonucleotide formyltransferase and efficacy of pemetrexed in advanced non-small cell lung cancer[J]. Anticancer Res, 20 12,32(10):4589-4596.
  • 8Kotoula V, Krikelis D, Karavasilis V,et al.Expression of DNA repair and replication genes in non-small cell lung cancer (NSCLC): a role for thymidylate synthetase (TYMS)[J]. BMC Cancer,2012, 1.2:342.
  • 9Ren SX ,Li A W ,Zhou SW .et al.Individualized chemotherapy in advanced NSCLC patients based on mRNA levels of BR?CA I and RRM I[J]. Chin J Cancer Res,201 2,24(3):226-23 1.
  • 10Reynolds C, Obasaju C, Schell MJ, et al. Randomized phase ill trial of gemcitabine-based chemotherapy with in situ RRM I and ERCC I protein levels for response predic?tion in non-small-cell lung cancer[J]. J Clin Oncol, 2009,27(34): 5808-5815.

共引文献11

同被引文献14

引证文献1

二级引证文献13

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