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机构地区:[1]重庆医科大学附属第一医院普外科,重庆400016
出 处:《中国癌症杂志》2007年第12期929-934,共6页China Oncology
基 金:重庆市卫生局科研项目(2007-2-029)
摘 要:背景与目的:CXCR4是趋化细胞因子SDF-1(基质细胞衍生因子-1)的受体。CXCR4/SDF-1轴在肿瘤侵袭,转移中具有重要作用。阻断CXCR4/SDF-1轴,有可能成为一个新的肿瘤治疗标靶。本研究拟探讨shR-NA-CXCR4对人乳腺癌细胞株MCF-7、MDA-MB-231、MDA-MB-435s细胞增殖活性的影响。方法:通过质粒shRNA-CXCR4沉默CXCR4基因后,RT-PCR,Westernblot检测3株人乳腺癌细胞的CXCR4mRNA及其蛋白的表达;MTT,流式细胞仪检测它们的增殖。结果:质粒shRNA-CXCR4作用于3株人乳腺癌细胞后能明显抑制其CXCR4基因的mRNA(MDA-MB-231:实验组CXCR4/GAPDH为0.152,空白组和阴性对照组分别为0.40及0.45,MDA-MB-435s:实验组为0.198,空白对照组和阴性对照组分别为0.690及0.775,MCF-7:实验组为0.089,空白对照组和阴性对照组分别为0.327及0.313)及蛋白表达水平(MDA-MB-231:实验组CXCR4/β-actin为0.153,空白组和阴性对照组分别为0.829及0.878,MDA-MB-435s:实验组为0.173,空白对照组和阴性对照组分别为0.877及0.906,MCF-7:实验组为0.177,空白对照组和阴性对照组分别为0.911及0.874)(P<0.05);MTT显示能明显抑制3株人乳腺癌细胞的增殖(P<0.05);流式细胞仪显示3株人乳腺癌细胞S期细胞数量明显减少(P<0.05),将更多的细胞阻滞在G0/G1期(P<0.05)。结论:shRNA-CXCR4作用于CXCR4基因后能明显抑制人乳腺癌细胞生长和增殖。可能是治疗乳腺癌的一个潜在治疗靶点。Background and purpose: A chemokine receptor, CXCR4, and its endogenous ligand, stromal cell-de- rixed factor-I ( SDF-I ), have been recognized to he involved in the invasion and metastasis of cancer. Inhibition of CXCR4 may be a new Iherapeutie target. We studied whether shRNA-CXCR4 could inhihit the CXCR4 gene expression and the proliferaliml in MCF-7, MDA-MB-231 and MDA-MB--435s breast eaneer eells. Methods: Through knockdown CXCR4 by shR- NA. the CXCR4 mRNA expression was detected by RT-PCR and the CXCR4 protein expression was mesured by Western biol. The proliferation of breast cancer eells was evaluated by MTF and flow cytometU. Results: The CXCR4mRNA and its pmlein expressiml decreased significantly in MCF-7( the average level of CXCR4 mRNA and protein expression were 0.089, 0.177 in PG-CXCR4 group, eompared with 0. 327 and 0. 313 for mRNA expression, 0. 911, 0.874 for protein expression in control and PG-HK group), MDA-MB-231( the average level of CXCR4 mRN A and protein expression were 0. 152 and 0. 153 in PG-CXCR4 group, compared with 0.40 and 0.45 for mRNA expression, 0.829 and 0.878 for protein expression in eontml and PG-HK group) and MDA-MB--435s( lhe average level of CXCR4 mRNA and protein expression were 0.198 and 0. 173 in PG-CXCR4 group, eompared with 0.69 and 0.77 for mRNA expression, 0. 877 and 0. 906 for protein expression in control and PG-HK group) breast cancer cells ( P 〈0.05). shRNACXCR4 could inhibit the cell proliferation( P 〈 0.05) and induce the cell eyele arrest at G0/ G1 phase with a signifieanl decrease of cells in S phase (P 〈0.05). Conclu- sions: Silencing CXCII4 enuhl inhibit the breast caneer growth. It may be a potentially valuable therapeutic target in the treatment of breast cancer.
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