摘要
目的探讨间质上皮转化因子(mesenchymal-epithelial transition factor,c-MET)m RNA在原发性肺腺癌组织中的表达及意义。方法回顾性分析2011年7月-2013年10月在我院手术并确诊的83例原发性肺腺癌患者的临床资料及c-MET m RNA检测结果。根据c-MET m RNA检测结果将患者分为高表达组和低表达组。结果 83例中,c-MET m RNA高表达占36.1%(30/83)。高表达组淋巴结转移率为46.7%(14/30),高于低表达组的20.8%(11/53)(P<0.05)。高表达组临床分期Ⅰ、Ⅱ、Ⅲ期分别为53.3%(16/30)、30.0%(9/30)、16.7%(5/30),低表达组为75.5%(40/53)、17.0%(9/53)、7.5%(4/53),两组有统计学差异(P<0.05)。高表达组的1年、2年无进展生存率为53.3%和22.2%,低表达组为81.1%和67.9%,两组无进展生存时间有统计学差异(P<0.05)。多因素分析显示,c-MET m RNA表达水平(HR=2.298,P=0.019)、分化程度(HR=2.632,P=0.003)和临床分期(HR=3.048,P=0.019)是肺腺癌预后的独立危险因素。结论 c-MET m RNA过度表达可能是原发性肺腺癌患者预后不良的因素。
Objective To investigate the expression and clinical significance of c-MET mRNA in primary lung adenocarcinoma. Methods Clinical data and c-MET mRNA test results about 83 patients with primary lung adenocarcinoma who underwent surgery in our hospital from July 2011 to October 2013 were retrospectively analyzed. Patients were divided into c-MET mRNA overexpression group and low expression group. Results In 83 patients, the constituent ratio of overexpression group was 36.1% (30/83). The lymph node metastasis rate of overexpression group and low expression group were 46.7% (14/30) and 20.8% (11/53) with significant difference (P 〈 0.05). The I , 11 , 11I TNM stage of overexpression group and low expression group were 53.3% (16/30), 30.0% (9/30), 16.7% (5/30) and 75.5% (40/53), 17.0% (9/53), 7.5% (4/53), which also showed significant differences (P 〈 0.05). The 1-, 2-year progression-free survival rate of overexpression group and low expression group were 53.3%, 22.2% and 81.1%, 67.9% with significant difference (P 〈 0.05). The multivariate analysis showed that c-MET mRNA level (HR=2.298, P=0.019), differentiation (HR=2.632, P=0.003) and TNM stage (HR=3.048, P=0.019) were independent risk factors for prognosis. Conclusion c-MET mRNA overexpression is a negative prognostic factor for patients with primary lung adenocarcinoma.
出处
《解放军医学院学报》
CAS
2015年第7期661-663,667,共4页
Academic Journal of Chinese PLA Medical School
关键词
非小细胞肺癌
腺癌
间质上皮转化因子基因
non-small cell lung cancer
adenocarcinoma
mesenchymal-epithelial transition factor gene