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作 者:时梅林[1] 白津[1] 梅鹏金[1] 郑骏年[1]
机构地区:[1]徐州医学院江苏省肿瘤生物治疗重点实验室,江苏徐州221002
出 处:《徐州医学院学报》2014年第12期830-834,共5页Acta Academiae Medicinae Xuzhou
基 金:基金项目:国家自然科学基金(81201636);江苏省自然科学基金(BK2012139)
摘 要:目的探讨沉默BRG1基因对乳腺癌细胞迁移和侵袭的影响及其分子机制。方法体外化学合成BRG1小干扰RNA(siRNA)和Control siRNA(si—Ctr1),脂质体介导转染乳腺癌MDA—MB-231和BT-549细胞,Transwell迁移实验和侵袭实验观察沉默BRG1基因对2种乳腺癌细胞迁移和侵袭能力的影响,明胶酶谱实验检测基质金属蛋白酶-2(matrix metalloproteinase-2,MMP-2)变化,Westernblot检测基质金属蛋白酶组织抑制因子-2(tissue inhibitor of metalloproteinase-2,TIMP-2)及MMP-2蛋白表达。结果转染BRG1 siRNA可以有效减少乳腺癌MDA—MB-231和BT-549细胞BRG1的表达,细胞迁移和侵袭能力下降。BRG1沉默后TIMP-2表达升高,MMP-2表达下降且酶活性降低。结论BRG1沉默后通过上调TIMP-2抑制MMP-2的表达,破坏TIMP-2/MMP-2平衡,最终抑制乳腺癌细胞迁移和侵袭能力。Objective To investigate the effect of silence of the Brahma - related gene 1 ( BRG1 ) in breast cancer cell lines on cell migration, invasion and its molecular mechanism. Methods Chemically synthesized small interfering RNA (siRNA) and control siRNA (si -Ctr1) targeting BRG1 were transfected into human breast cancer cell lines by si- LentFect lipid reagent. The migration ability of two breast cancer cells was detected by cell migration assay. The invasive ability was detected by cell invasion assay. The matrix metalloproteinase -2 (MMP- 2) enzyme activities were detected by gelatin zymography and the MMP - 2 and tissue inhibitor of metalloproteinase - 2 ( TIMP - 2 ) protein expressions were detected by Western blot. Results BRG1 interference could drastically decreased the ability of cell invasion and migra- tion in both breast cancer cells. The Western blot results showed that BRG1 knock - down increased TIMP - 2 and de- creased MMP - 2 expression. BRG siRNA could also suppress MMP - 2 enzyme activity. Conclusions Silence of BRG1 can suppress human breast cancer cell invasion through up - regulation of TIMP - 2 and down - regulation of MMP - 2.
关 键 词:乳腺癌 侵袭 迁移 BRG1 基质金属蛋白酶-2 基质金属蛋白酶组织抑制因子-2
分 类 号:R329.2[医药卫生—人体解剖和组织胚胎学]
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