山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2015年
14期
19-21
,共3页
魏西军%王清路%李俏俏%江小华
魏西軍%王清路%李俏俏%江小華
위서군%왕청로%리초초%강소화
金属硫蛋白%乳腺癌细胞%细胞色素C氧化酶6B2亚基
金屬硫蛋白%乳腺癌細胞%細胞色素C氧化酶6B2亞基
금속류단백%유선암세포%세포색소C양화매6B2아기
metallothionein%breast cancer cells%cytochrome C oxidase 6B2 subunit
目的:探讨金属硫蛋白2A( MT2A)基因沉默对乳腺癌细胞呼吸链中细胞色素 C 氧化酶6B2亚基( Cpy6B2)表达的影响。方法乳腺癌野生细胞株MCF-7(以下简称MCF-7)分为空白对照组和MT2A干扰组,每组各12复孔。空白对照组不转染任何遗传物质, MT2A干扰组转染shRNA-MT2A载体,采用半定量PCR法检测两组MT2A mRNA的表达水平,MT2A干扰组成功获得 MT2A基因沉默,采用实时定量PCR法分析两组Cpy6B2的表达水平。结果 MT2A干扰组中Cpy6B2的表达水平升高,与空白对照组相比,P<0.05。结论 MT2A基因可抑制人乳腺癌细胞Cpy6B2的表达。
目的:探討金屬硫蛋白2A( MT2A)基因沉默對乳腺癌細胞呼吸鏈中細胞色素 C 氧化酶6B2亞基( Cpy6B2)錶達的影響。方法乳腺癌野生細胞株MCF-7(以下簡稱MCF-7)分為空白對照組和MT2A榦擾組,每組各12複孔。空白對照組不轉染任何遺傳物質, MT2A榦擾組轉染shRNA-MT2A載體,採用半定量PCR法檢測兩組MT2A mRNA的錶達水平,MT2A榦擾組成功穫得 MT2A基因沉默,採用實時定量PCR法分析兩組Cpy6B2的錶達水平。結果 MT2A榦擾組中Cpy6B2的錶達水平升高,與空白對照組相比,P<0.05。結論 MT2A基因可抑製人乳腺癌細胞Cpy6B2的錶達。
목적:탐토금속류단백2A( MT2A)기인침묵대유선암세포호흡련중세포색소 C 양화매6B2아기( Cpy6B2)표체적영향。방법유선암야생세포주MCF-7(이하간칭MCF-7)분위공백대조조화MT2A간우조,매조각12복공。공백대조조불전염임하유전물질, MT2A간우조전염shRNA-MT2A재체,채용반정량PCR법검측량조MT2A mRNA적표체수평,MT2A간우조성공획득 MT2A기인침묵,채용실시정량PCR법분석량조Cpy6B2적표체수평。결과 MT2A간우조중Cpy6B2적표체수평승고,여공백대조조상비,P<0.05。결론 MT2A기인가억제인유선암세포Cpy6B2적표체。
Objective To investigate the effect of metallothionein 2A ( MT2A) silencing on cytochrome C oxidase 6B2 subunit (Cpy6B2) expression of breast cancer cells .Methods The breast cancer wild cell line MCF-7 (hereinafter referred as the MCF-7) was divided into the blank control group and MT 2A interference group, and each group had 12 holes.The blank control group did not transfect any genetic materials , and the MT2A interference group transfected the shRNA-MT2A vector.Using semi-quantitative PCR to detect the MT2A mRNA expression levels of the two groups .The MT2A interference group successfully obtained the MT 2A gene silencing .The real-time quantitative PCR was used to ana-lyze the expression of Cpy6B2 in the two groups.Results The results showed that the expression level of MCF-7 Cpy6B2 was increased under the MT2A gene silencing.Conclusion MT2A can inhibit the Cpy6B2 expression of breast cancer cells.