首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Lewis (y) Antigen Overexpression Increases the Expression of MMP-2 and MMP-9 and Invasion of Human Ovarian Cancer Cells
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Lewis (y) Antigen Overexpression Increases the Expression of MMP-2 and MMP-9 and Invasion of Human Ovarian Cancer Cells

机译:Lewis(y)抗原过表达增加MMP-2和MMP-9的表达以及对人卵巢癌细胞的侵袭

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摘要

Lewis (y) antigen is a difucosylated oligosaccharide present on the plasma membrane, and its overexpression is frequently found in human cancers and has been shown to be associated with poor prognosis. Our previous studies have shown that Lewis (y) antigen plays a positive role in the process of invasion and metastasis of ovarian cancer cells. However, the mechanisms by which Lewis (y) antigen enhances the invasion and tumor metastasis are still unknown. In this study, we established a stable cell line constitutively expressing Lewis (y) antigen (RMG-1-hFUT) by transfecting the cDNA encoding part of the human α1,2-fucosyltransferase (α1,2-FUT) gene into the ovarian cancer cell line RMG-1, and investigated whether Lewis (y) antigen regulates the expression of matrix metalloproteinase-2 (MMP-2) and MMP-9, and tissue inhibitors of metalloproteinases (TIMP-1) and TIMP-2. We found that RMG-1-hFUT cells exhibited higher invasive capacities than their control cells. In addition, expression of TIMP-1 and TIMP-2 was down-regulated and expression of MMP-2 and MMP-9 was up-regulated. Anti-Lewis (y) antigen antibody treatment significantly reversed the expression of TIMP-1, TIMP-2, MMP-2 and MMP-9. Taken together, we provide the first evidence that down-regulation of TIMP-1 and TIMP-2 and up-regulation of MMP-2 and MMP-9 represents one of the mechanisms by which Lewis (y) antigen promotes cell invasion.
机译:Lewis(y)抗原是存在于质膜上的双岩藻糖基化寡糖,其过表达在人类癌症中经常发现,并已显示与不良预后有关。我们以前的研究表明,路易斯(y)抗原在卵巢癌细胞的侵袭和转移过程中起着积极的作用。然而,Lewis(y)抗原增强侵袭和肿瘤转移的机制仍是未知的。在这项研究中,我们通过将编码人α1,2-岩藻糖基转移酶(α1,2-FUT)基因的一部分的cDNA转染到卵巢癌中,从而建立了组成型表达Lewis(y)抗原(RMG-1-hFUT)的稳定细胞系细胞系RMG-1,并研究Lewis(y)抗原是否调节基质金属蛋白酶2(MMP-2)和MMP-9的表达,以及金属蛋白酶组织抑制剂(TIMP-1)和TIMP-2。我们发现RMG-1-hFUT细胞显示出比其对照细胞更高的侵袭能力。另外,TIMP-1和TIMP-2的表达下调,而MMP-2和MMP-9的表达上调。抗刘易斯(y)抗原抗体治疗显着逆转了TIMP-1,TIMP-2,MMP-2和MMP-9的表达。综上所述,我们提供了第一个证据,即TIMP-1和TIMP-2的下调以及MMP-2和MMP-9的上调代表了Lewis(y)抗原促进细胞侵袭的机制之一。

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