郭杨, 王永利, 王小玲, 杨会钗, 王永军. 耐药相关基因在非小细胞肺癌组织中的表达及其意义[J]. 中国肿瘤临床, 2004, 31(7): 391-394.
引用本文: 郭杨, 王永利, 王小玲, 杨会钗, 王永军. 耐药相关基因在非小细胞肺癌组织中的表达及其意义[J]. 中国肿瘤临床, 2004, 31(7): 391-394.
Guo Yang, Wang Yong-li, Wang Xiao-ling, . Expression and Clinical Significance of Resistance-Related Genes in Non-small Cell Lung Cancer Tissue[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(7): 391-394.
Citation: Guo Yang, Wang Yong-li, Wang Xiao-ling, . Expression and Clinical Significance of Resistance-Related Genes in Non-small Cell Lung Cancer Tissue[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(7): 391-394.

耐药相关基因在非小细胞肺癌组织中的表达及其意义

Expression and Clinical Significance of Resistance-Related Genes in Non-small Cell Lung Cancer Tissue

  • 摘要: 目的:探讨耐药相关基因在非小细胞肺癌(NSCLC)组织中的表达及其临床意义.方法:应用免疫组化技术检测治疗前肺癌组织标本中P-gp、MRP、LRP、GST-π和TopoII表达.结果:58例治疗前NSCLC中P-gp、MRP、LRP、GST-π和TopoII阳性率分别为96.55%,67.24%,75.86%,65.52%,98.28%,并有部分共表达.癌旁正常肺组织呈阴性或弱阳性表达.性别、有无吸烟史、有无淋巴结转移及在TNM各分期中P-gp、MRP、LRP、GST-π和TopoII阳性表达无明显差异(P>0.05).比较腺癌组与鳞癌组,MRP、LRP、GST-π阳性表达有显著性差异(P<0.05),而P-gp、TopoII阳性表达无明显差异(P>0.05);MRP、LRP、P-gp、GST-π共表达有显著性差异(χ2=21.662,P<0.001);低分化腺癌、鳞癌与中、高分化腺癌、鳞癌P-gp、MRP、LRP、GST-π和TopoII阳性表达无明显差异(P>0.05).结论:肺癌耐药为一多途径多基因参与的过程,肺腺癌原发的多药耐药机率较肺鳞癌高,联合检测肺癌组织中耐药相关基因的表达有助于判断化疗疗效及预后.

     

    Abstract: Objective: To investigate the expression and clinical significance of resistance-related genes in non-small cell lung cancer tissue. Methods: Expression of P-glycoprotein (P-gp), multidrug resistance -associated protein(MRP), lung resistance pretein(LRP), glutathione Stransferases (GST) and DNA topoisomerase II (Topo) in lung carcinoma tissue from untreated patients was measured by im-munohistochemistry technique. Results: The Positive rates of P-gp, MRP, LRP, GST-π and Topo II which were negative or weakly positive in the normal pericarcinoma tissues and expressed together in part of samples among 58 untreated patients were 96.55%, 67.24%, 75.86%, 65.52R and 98.28R re-spectively, which were not markedly correlated to sex, smoke history, TNM staging, differentiated degree and lymph node metastasis (P>0.05). There were statistic difference in MRP, LRP and GST-π expression(P<0.05) and no marked difference in P-gp and Topo II between squamous carcinoma and adeno-carcinoma (P>0.05). Conclusion: Multidrug resistance of lung cancer is a process involved in polygene and multiple pathways, which is more common in adenocarcinoma compared with squamous carcinoma Combined examination of resistance-related genes in lung cancer tissues is helpful to the judgement of chemotherapeutics effects and prognosis.

     

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