刘毅梅, 张鹏, 陈洁, 陈刚, 杨萍. 非小细胞肺癌患者骨髓CK19和LUNX mRNA的实时荧光定量检测和意义[J]. 中国肿瘤临床, 2006, 33(17): 988-991.
引用本文: 刘毅梅, 张鹏, 陈洁, 陈刚, 杨萍. 非小细胞肺癌患者骨髓CK19和LUNX mRNA的实时荧光定量检测和意义[J]. 中国肿瘤临床, 2006, 33(17): 988-991.
Liu Yimei, Zhang Peng, Chen Jie, Chen Gang, Yang Ping. Detection and significance of CK19 mRNA and LUNX mRNA in bone marrow of Non-small Cell Lung Cancer patients by FQ-RT-PCR[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(17): 988-991.
Citation: Liu Yimei, Zhang Peng, Chen Jie, Chen Gang, Yang Ping. Detection and significance of CK19 mRNA and LUNX mRNA in bone marrow of Non-small Cell Lung Cancer patients by FQ-RT-PCR[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(17): 988-991.

非小细胞肺癌患者骨髓CK19和LUNX mRNA的实时荧光定量检测和意义

Detection and significance of CK19 mRNA and LUNX mRNA in bone marrow of Non-small Cell Lung Cancer patients by FQ-RT-PCR

  • 摘要: 目的 :检测非小细胞肺癌患者CK19mRNA和LUNXmRNA的表达情况,探讨其作为微转移检测分子标志物的可行性。 方法 :选择初治的非小细胞肺癌(NSCLC)患者62例,以肺部良性疾病10例作为对照组,采用实时荧光定量逆转录聚合酶链反应(FQ-RT-PCR)和普通RT-PCR技术,检测肺癌、良性病变肺组织和骨髓的CK19mRNA和LUNXmRNA的表达。 结果 :肺癌和良性病变肺组织RT-PCR检测结果显示CK19mRNA和LUNXmRNA表达阳性率为100%;62例NSCLC患者骨髓标本FQ-RT-PCR检测结果显示,NSCLC患者中骨髓CK19mRNA表达阳性率45.2%(28/62),明显高于肺良性病变组10%(1/10)(P=0.037),NSCLC组骨髓LUNXmRNA表达阳性率38.7%(24/62)明显高于肺良性病变组0%(0/10)(P=0.017);骨髓CK19mRNA表达阳性率随病理分期升高,接近统计学意义(P=0.06),而与病理类型、肿瘤分化程度无关;骨髓LUNXmRNA表达阳性率随分期升高且有统计学意义(P=0.02),而与病理类型、肿瘤分化程度无关;骨髓CK19mRNA和LUNXmRNA表达明显相关(P<0.001)。 结论 :CK19mRNA和LUNXmRNA可作为检测非小细胞肺癌患者微转移特异、敏感的分子标志物,可能有助于早期诊断肺癌转移,从而指导临床分期和治疗。

     

    Abstract: Objective : Detection of CK19 mRNA and LUNX mRNA in bone marrow of non - small cell lung cancer (NSCLC) patients in order to discuss the possibility of indicating lung cancer micrometastases by them. Methods : Fluorescence quantitative reverse transcription-polymerase chain reaction (FQ-RT-PCR) and ordinary RT- PCR was used to detect CK19 mRNA and LUNX mRNA in cancer tissue and bone marrow from 62 patients with NSCLC. Lung tissue and bone marrow from 10 patients with benign pulmonary diseases were served as controls. Results : CK19 mRNA and LUNX mRNA was expressed in all the lung tissues, either malignant or benign. In bone marrow, the positive rate of CK19 mRNA for NSCLC was 45.2% (28/62) vs 10%(1/10) in benign controls(P=0.037), the positive rate of LUNX mRNA for NSCLC was 38.7%(24/62) vs 0%(0/10) in benign controls (P=0.017). The positive rate of CK19 mRNA for NSCLC in bone marrow increases according to the stage of disease and nearly reaches a statistical significance (P=0.06), the positive rate of LUNX mRNA for NSCLC in bone marrow increases according to the stage of disease and there is a statistical significance (P=0.02), and for the positive expression in bone marrow of NSCLC there is a relationship between CK19 mRNA and LUNX mRNA (P<0.001). Conclusion : CK19 mRNA and LUNX mRNA are efficient indicating factors on sensitivity and specificity to detect early haematogenous dissemination of cancer cells for patients with NSCLC. This method may lead to an earlier diagnosis of metastasis for lung cancer and do some help to evaluate the cancer more correctly and make the best treatment plan.

     

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