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ADHESION INDUCES MATRIX METALLOPROTEINASE-9 GENE EXPRESSION IN OVARIAN CANCER CELLS

机译:粘附诱导卵巢癌细胞中基质金属蛋白酶9基因的表达

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Objective: To investigate the expression of matrix metalloproteinase-9 (MMP-9) gene in cancer cells induced by adhesion with fibronectin and the underlying mechanism of cell invasion. Methods: Following adhesion of ovarian cancer cells A2780 to fibronectin, MMP mRNA expression was assayed by using reverse transcription-polymerase chain reaction (RT-PCR). MMP-9 promoter was cloned from genomic DNA of HT1080 cells with PCR. The MMP-9-pGL2 reporter gene vector was constructed and then transiently transfected into A2780 cells. Results: Adhesion could induce the expression of MMP-9 gene in A2780 cells, but did not affect longer theexpression of MMP-2 or TIMP-1 gene. The induction was enhanced with longer adhesion time. When the transfected cells were allowed to adhere and spread on FN-coated surface, the promoter activity of MMP-9 gene was also enhanced dramatically. Conclusion: adhesion of cells with ECM may stimulate the expression of MMP-9 gene through stimulating the promoter activity, thereby enhancing cancer cell invasion and metastasis.
机译:目的:探讨基质金属蛋白酶9(MMP-9)基因在纤连蛋白粘附诱导的癌细胞中的表达及其潜在的侵袭机制。方法:在卵巢癌细胞A2780粘附于纤连蛋白后,采用逆转录聚合酶链反应(RT-PCR)检测MMP mRNA的表达。通过PCR从HT1080细胞的基因组DNA中克隆出MMP-9启动子。构建了MMP-9-pGL2报告基因载体,然后瞬时转染到A2780细胞中。结果:黏附可以诱导A2780细胞中MMP-9基因的表达,但不会影响MMP-2或TIMP-1基因的较长表达。更长的粘附时间增强了诱导。当转染的细胞粘附并在FN包被的表面上铺展时,MMP-9基因的启动子活性也大大提高。结论:细胞与ECM的粘附可能通过刺激启动子活性来刺激MMP-9基因的表达,从而增强癌细胞的侵袭和转移能力。

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