期刊文献+

非小细胞肺癌区域淋巴结中肺组织特异性基因的表达与预后的关系 被引量:7

mRNA expression of lunx in regional lymph nodes of non-small cell lung cancer and its correlation with prognosis
下载PDF
导出
摘要 目的:探讨非小细胞肺癌(non-small-cell lung cancer,NSCLC)区域淋巴结人肺组织特异性基因(lunx mRNA)的表达与预后的关系。方法:应用SYBR GreenⅠ嵌合荧光法进行逆转录聚合酶链反应(real-timeRT-PCR)用以检测74例NSCLC手术切除区域淋巴结Lunx mRNA的表达,对入选患者进行为期3年的随访观察,并对6个可能影响NSCLC患者预后的因素进行Cox回归模型分析。结果:手术切除区域淋巴结Lunx表达率与年龄、营养指数、3年内的复发或转移率之间有相关性(P<0.01,P<0.01,P<0.05),而患者的性别、肺癌病理类型、分期与手术切除区域淋巴结Lunx表达率之间无相关性(P>0.05);NSCLC患者的生存时间与术后辅助治疗及与Lunx表达有统计学意义(P<0.05,P<0.01)。结论:NSCLC患者Lunx mRNA表达与其生存时间显著相关,提示Lunx mRNA可作为NSCLC淋巴微转移的分子标志物及监测患者3年预后的指标之一;同时术后辅助治疗是延长患者生存时间的一项重要措施;荧光实时RT-PCR相对定量方法可应用于NSCLC淋巴微转移的检测,该方法可能有助于早期肺癌转移的诊断。 Objective: To explore the mRNA expression of lunx in regional lymph nodes of non-small cell lung cancer (NSCLC) and its correlation with prognosis. Methods SYBR green I real-time RT-PCR was used to detemine the lunx mRNA level in 153 regional lymph nodes obtained from 75 patients with NSCLC. All patients had been followed up for 3 years. Six factors that may influence the survival rate were analyzed by a Cox regression model. Results: Expressions of lunx in regional lymph nodes had a statistical correlation with age, nutritional index, relapse within 3 years and metastasis( P 〈 0.01, P 〈 0.01, and P 〈 0.05) but had no correlation with gender, tumor types and pathological grades( P 〉 0.05). There were statistical significances between the survival of NSCLC patients and post-operative adjuvant therapy and expression of lunx (P 〈 0.05 and P 〈 0.01). Conclusions: The expression of Lunx in regional lymph nodes closely correlates with the survival of NSCLC patients and it may be a target gene for detection of micrometastasis from NSCLC and a marker for detection in 3 years prognosis. Quantitative real-time RT-PCR is helpful in early diagnosis of micrometastasis of the lymph node in patients with NSCLC.
出处 《山东大学学报(医学版)》 CAS 北大核心 2007年第9期882-885,共4页 Journal of Shandong University:Health Sciences
关键词 肺肿瘤 微转移 人肺组织特异性基因 逆转录聚合酶链反应 Lung neoplasms Micrometastasis Lunx RT-PCR
  • 相关文献

参考文献9

  • 1Wallace M B,Block M I,Gillanders W,et al.Accurate molecular detection of non-small cell lung cancer metastases in mediastinal lymph nodes sampled by endoscopic ultrasound-guided needle aspiration[J].Chest,2005,127(2):430-437.
  • 2Sher Y P,Shih J Y,Yang P C,et al.Prognosis of non-small cell lung cancer patients by detecting circulating cancer cells in the peripheral blood with multiple maker genes[J].Clin Cancer Res,2005,11(1):173-179.
  • 3Mitas M,Hoover L,Silvestri G,et al.Lunx is a superior molecular marker for detection of non-small cell lung cancer in peripheral blood[J].J Mol Diagn,2003,5(4):237-242.
  • 4Iwao K,Watanabe T,Fujiwara K,et al.Isolation of a novel human lung-specific gene,LUNX,a potential molecular marker for detection of micro-metastasis in non-small-cell lung cancer[J].Int J Cancer,2001,91(4).
  • 5张驰宇,徐顺高,黄新祥.一种新颖简便的荧光实时RT-PCR相对定量方法的建立[J].生物化学与生物物理进展,2005,32(9):883-888. 被引量:129
  • 6Livak K J,Schmittgen T D.Analysis of relative gene expression data using real-time quantitative PCR and the 2 (-Delta Delta C(T)method[J].Methods,2001,25(4):402-408.
  • 7朱广迎,刘德林,王绪,彭猛青,陈杰,贾晓民.lunx mRNA RT-PCR检测肺癌的微转移[J].中国肿瘤临床,2003,30(2):124-127. 被引量:15
  • 8黄同海,王正,李富荣,齐晖,任莉莉,周汉新.巢式PCR检测肺癌患者外周血CK19 mRNA和LUNX mRNA的临床意义[J].广东医学,2007,28(2):236-238. 被引量:5
  • 9Mitas M,Hoover L,Silvestri G,et al.Lunx is a superior molecular marker for detection of non-small lung cell cancer in pefipheral blood[J].J Mol Diagn,2003,5(4):237-242.

二级参考文献14

  • 1徐顺高,黄新祥,周丽萍.荧光实时定量RT-PCR观察伤寒杆菌鞭毛z66和d/j抗原基因表达方法的建立[J].江苏大学学报(医学版),2005,15(1):21-24. 被引量:3
  • 2Bustin S A. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. J Mol Endocrinol, 2000, 25 (2): 169~193.
  • 3Giulietti A, Overbergh L, Valckx D, et al. An overview of real-time quantitative PCR: applications to quantify cytokine gene expression.Methods, 2001, 25 (4): 386~401.
  • 4Livak K J, Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2 (-Delta Delta C (T))Method. Methods, 2001, 25 (4): 402~408.
  • 5Liu W, Saint D A. A new quantitative method of real time reverse transcription polymerase chain reaction assay based on simulation of polymerase chain reaction kinetics. Anal Biochem, 2002, 302 (1):52~59.
  • 6SPIRA A,ETTINGER DS.Multidisciplinary management of lung cancer[J].N Engl J Med,2004,350(19):379-392.
  • 7MOCELLIN S,KEILHOLZ U,ROSSI C R,et al.Circulating tumor cells:the 'leukemic phase' of solid cancers[J].Trends Mol Med,2006,12(3):130-139.
  • 8SCHULER F,DOLKEN G.Detection and monitoring of minimal residual disease by quantitative real-time PCR[J].Clin Chim Acta,2006,363 (1-2):147-156.
  • 9ZIPPELIUS A,PANTEL K.RT -PCR -based detection of occult disseminated tumor cells in peripheral blood and bone marrow of patients with solid tumors.An overview[J].Ann N Y Acad Sci,2000,906:110-123.
  • 10IWAO K,WATANABE T,FUJIWARA Y,et al.Isolation of a novel human lung-specific gene,LUNX,a potential molecular marker for detection of micrometastasis in non-small-cell lung cancer[J].Int J Cancer,2001,91 (4):433 -437.

共引文献142

同被引文献73

引证文献7

二级引证文献15

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