基础医学与临床
基礎醫學與臨床
기출의학여림상
Basic & Clinical Medicine
2015年
1期
44-47
,共4页
林剑勇%邓益斌%罗艳红%陆小婵%黄永秩
林劍勇%鄧益斌%囉豔紅%陸小嬋%黃永秩
림검용%산익빈%라염홍%륙소선%황영질
肺肿瘤%miRNA-449 a%肿瘤标志%聚合酶链反应%荧光定量
肺腫瘤%miRNA-449 a%腫瘤標誌%聚閤酶鏈反應%熒光定量
폐종류%miRNA-449 a%종류표지%취합매련반응%형광정량
lung neoplasms%miRNA-449a%tumor biomarker%polymerase chain reaction%fluorogenic quantitative
目的:探讨miRNA-449a在人肺癌及癌旁组织中的表达差异及其临床意义。方法右江民族医学院附属医院2011-01-01—2013-06-30收治的肺癌患者58例,对照组为癌旁正常组织,病例组为鳞癌组织和腺癌组织,并根据miRNA-449 a序列结构设计合成miRNA-449 a模拟物,设10和20 mg/mL两个不同浓度,以0 mg/mL为阴性对照,用real-time PCR检测肺癌及其对应癌旁组织中miRNA-449 a的表达;化学发光技术检测细胞内荧光素酶基因表达;四甲基偶氮唑蓝法检测细胞活性。结果鳞癌组和腺癌组的miRNA-449a的表达量为1.48±1.63和1.52±1.54,均显著低于癌旁正常对照组的2.74±1.55( P<0.01),且与瘤体大小有关( P<0.05)。10和20 mg/mL 组细胞内的平均荧光强度为2115±168和1352±159,均显著低于阴性对照组的4975±115( P<0.01),且抑制作用随浓度增加呈递增趋势。结论 miRNA-449 a在肺癌组织中呈低表达,可下调细胞内荧光蛋白表达和诱导细胞凋亡。
目的:探討miRNA-449a在人肺癌及癌徬組織中的錶達差異及其臨床意義。方法右江民族醫學院附屬醫院2011-01-01—2013-06-30收治的肺癌患者58例,對照組為癌徬正常組織,病例組為鱗癌組織和腺癌組織,併根據miRNA-449 a序列結構設計閤成miRNA-449 a模擬物,設10和20 mg/mL兩箇不同濃度,以0 mg/mL為陰性對照,用real-time PCR檢測肺癌及其對應癌徬組織中miRNA-449 a的錶達;化學髮光技術檢測細胞內熒光素酶基因錶達;四甲基偶氮唑藍法檢測細胞活性。結果鱗癌組和腺癌組的miRNA-449a的錶達量為1.48±1.63和1.52±1.54,均顯著低于癌徬正常對照組的2.74±1.55( P<0.01),且與瘤體大小有關( P<0.05)。10和20 mg/mL 組細胞內的平均熒光彊度為2115±168和1352±159,均顯著低于陰性對照組的4975±115( P<0.01),且抑製作用隨濃度增加呈遞增趨勢。結論 miRNA-449 a在肺癌組織中呈低錶達,可下調細胞內熒光蛋白錶達和誘導細胞凋亡。
목적:탐토miRNA-449a재인폐암급암방조직중적표체차이급기림상의의。방법우강민족의학원부속의원2011-01-01—2013-06-30수치적폐암환자58례,대조조위암방정상조직,병례조위린암조직화선암조직,병근거miRNA-449 a서렬결구설계합성miRNA-449 a모의물,설10화20 mg/mL량개불동농도,이0 mg/mL위음성대조,용real-time PCR검측폐암급기대응암방조직중miRNA-449 a적표체;화학발광기술검측세포내형광소매기인표체;사갑기우담서람법검측세포활성。결과린암조화선암조적miRNA-449a적표체량위1.48±1.63화1.52±1.54,균현저저우암방정상대조조적2.74±1.55( P<0.01),차여류체대소유관( P<0.05)。10화20 mg/mL 조세포내적평균형광강도위2115±168화1352±159,균현저저우음성대조조적4975±115( P<0.01),차억제작용수농도증가정체증추세。결론 miRNA-449 a재폐암조직중정저표체,가하조세포내형광단백표체화유도세포조망。
Objective To investigate the expression and biological function of miRNA-449 a in lung cancer . Methods A case-control study was conducted in 58 patients diagnosed with lung cancer ( carcinoma and adeno-carcinoma) and normal tissue closely adjacent to tumor.MiRNA-449a simulation was designed and synthesized, was dissolved into two different concentrations as 10 and 20 mg/mL.The expression of miRNA-449a in lung cancer tissues and matched normal tissues were detected by Real time PCR .The expression of luciferase gene was detected by chemiluminescence technique.MiRNA-449a mimics on cell apoptosis was evaluated by MTT assay . Results The mean tissues expression levels of miRNA-449 a in squamous carcinoma group and adenocarcinoma group were 1.48 ±1.63 and 1.52 ±1.54 respectively, and were significantly lower than in control group (2.74 ± 1.55 ) ( P<0.01 ) .The average intensity of fluorescent protein in 10 mg/mL group and 20 mg/mL group were 2 115 ±168 and 1 352 ±159 respectively , and were significantly lower than that in control group ( 4 975 ±115 ) ( P<0.01 ) .Conclusions MiRNA-449 a was down-regulated expression in lung cancer and induced apoptosis .