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作 者:成党校[1] 钱桂生[2] 金发光[1] 黄桂君[2] 王建丽[1]
机构地区:[1]第四军医大学唐都医院呼吸科,西安710038 [2]第三军医大学新桥医院呼吸内科研究所,重庆630037
出 处:《基础医学与临床》2001年第5期412-415,共4页Basic and Clinical Medicine
基 金:国家自然科学基金 (3990 0 0 6 7)
摘 要:本文应用RT PCR方法扩增了人正常肺组织、肺癌组织中的MCT1、MCT2及 β actin基因mRNA ,以人 β actin基因RT PCR产物作为外参照 ,通过比较同一样本组中及样本组间MCT1、MCT2相对于 β actin的RT PCR产物的光密度比值 ,来分析判断MCT1、MCT2mRNA表达的高低。结果显示 ,MCT1在人正常肺组织、肺癌组织中的mRNA表达均高于MCT2 ;MCT1、MCT2基因mRNA在人肺癌组织中的表达明显高于癌旁正常肺组织。The mRNA of MCT1,MCT2 and β actin in normal lung tissue and lung cancer tissue were amplified by RT PCR method; mRNA expression of MCT1 and MCT2 in tissue samples was semi quantitatively analyzed by comparing the relative ratio of MCT1 and MCT2 RT PCR product's OD ( optical density) vs.β actin RT PCR product's OD (β actin as an extecnae standard) . The results show that mRNA expression of MCT1 is significant higher than MCT2 in human normal lung tissue and lung cancer tissue; In human lung cancer tissue, the mRNA expression of MCT1 and MCT2 is significant higher than in that in the human normal lung tissue. Our data indicated that MCT1 might play an important role in intracellular pH regulation of tumor cells.
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