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机构地区:[1]复旦大学附属中山医院重症监护室,上海200032 [2]复旦大学附属中山医院普外科,上海200032
出 处:《中国临床医学》2014年第2期134-136,共3页Chinese Journal of Clinical Medicine
摘 要:目的:研究印记基因SLC22A18(solute carrier family 22,member 18)在乳腺癌中的表达情况及其与乳腺癌侵袭能力的关系。方法:采用Transwell方法评估2种不同恶性程度的乳腺癌细胞株MDA-MB-231(恶性程度高)和MCF-7(恶性程度低)的侵袭转移能力。分别采用实时荧光定量逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法检测SLC22A18的mRNA和蛋白在这2种乳腺癌细胞株中的表达情况。结果:MDA-MB-231细胞株恶性程度高,穿过膜的细胞多,侵袭能力强;MCF-7细胞株恶性程度低,穿过膜的细胞少,侵袭能力弱;SLC22A18在MCF-7中的mRNA和蛋白表达水平高于MDA-MB-231;差异有统计学意义(P<0.01)。结论:印记基因SLC22A18的表达与乳腺癌细胞的侵袭能力相关,该基因有望作为一个抑癌基因抑制乳腺癌的转移。Objective:To assess the expression of imprinted gene SLC22A18 (solute carrier family 22, member 18)in human breast cancer and its relationship with the invasion of human breast cancer. Methods:Transwell assay was used to evaluate the invasion abilities of two breast cancer cell lines MDA-MB-231 (with high metastatic ability) and MCF-7 (with low metastatic ability). Real time fluorescence quantitative reverse transcriptase-polymerase chain reaction and Western blotting was used to detect the mRNA and protein levels of SLC22A18 in the two breast cancer cell lines. Results: There were much more MDA- MB-231cells that passed through the Matrigel membrane than MCF-7. The invasion abilities of the two breast cancer cell lines were significantly different(P〈0.01), mRNA and protein levels of SLC22A18 in MDA-MB-231 were significantly lower than those in MCF-7(P〈0.01 ). Conclusions: SLC22A18 expression has correlation with the invasion abilities of human breast cancer cells. SLC22A18 may serve as a tumor suppressor gene which can restrain the invasion abilities of human breast cancer cells.
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