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作 者:田玉旺[1] 许春伟[1] 高文斌[2] 张玉萍[3] 李扬[4] 亓岽东[2]
机构地区:[1]解放军北京军区总医院病理科,100700 [2]大连大学附属中山医院肿瘤科,116001 [3]山东省潍坊市人民医院病理科,261041 [4]解放军北京军区总医院肿瘤内科诊治中心,100700
出 处:《中华肺部疾病杂志(电子版)》2014年第2期12-15,共4页Chinese Journal of Lung Diseases(Electronic Edition)
基 金:吴阶平医学基金会临床科研专项资助基金(320.6750.1360)
摘 要:目的探讨非小细胞肺癌(nonsmall-cell lung cancer,NSCLC)组织中棘皮动物微管样蛋白4-间变淋巴瘤激酶(echinoderm microtubule associated protein like 4-anaplastic Lymphoma kinase,EML4-ALK)融合基因与胸苷酸合成酶(Thymidylate synthase,TYMS)mRNA表达的关系。方法应用实时荧光定量PCR方法检测257例NSCLC组织中EML4-ALK融合基因、TYMS mRNA的表达。结果非小细胞肺癌组织中EML4-ALK融合基因阳性率占4.28%(11/257),在不吸烟患者中较高(P<0.05);TYMS mRNA高表达占63.42%(163/257)。与未检测到EML4-ALK融合基因阳性的非小细胞肺癌患者比较,EML4-ALK融合基因阳性与TYMS mRNA表达水平相关(P<0.05)。结论非小细胞肺癌组织中EML4-ALK融合基因阳性患者TYMS倾向低表达,可能从一线化疗药的培美曲塞中受益。Objective Explore echinoderm microtubule in nonsmall-cell lung cancer tissue-like protein 4-anaplastic Lymphoma kinase echinoderm mierotubule associated protein like 4-anaplastie Lymphoma kinase Fusion gene and Thymidylate synthetase relationship between mRNA expression. Methods Application of real-time fluorescent quantitative PCR method for detection of 257 cases of nonsmall-cell lung cancer echinoderm microtubule associated protein like 4-anaplastic Lymphoma kinase fusion gene, Thymidylate synthase mRNA expression in the tissue. Results echinoderm microtubule associated protein like 4-anaplastic Lymphoma kinase fusion gene-positive rate in nonsmall-eell lung cancer tissue (4.28%), not in smokers is higher ( P 〈 0. 05 ) ; Thymidylate synthase mRNA overexpression ( 63. 42% ). With the echinoderm microtubule associated protein like 4-anaplastic Lymphoma kinase fusion gene was not detected-positive nonsmall-cell lung cancer compared with echinoderm microtubule associated protein like 4-anaplastie Lymphoma kinase fusion gene-positive and Thymidylate synthase mRNA expression levels ( P 〈 0.05 ). Conclusions In nonsmall-cell lung cancer tissue echinoderm microtubule associated protein like 4-anaplastic Lymphoma kinase Thymidylate synthase low expression of fusion gene-positive patients may benefit from first-line chemotherapy drugs in Pemetrexeddisodium.
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