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Peroxisome proliferator‐activated receptor‐γ activation inhibits hepatocellular carcinoma cell invasion by upregulating plasminogen activator inhibitor‐1

机译:过氧化物体增殖剂活化受体-γ活化通过上调纤溶酶原激活剂抑制剂-1抑制肝细胞癌细胞侵袭

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摘要

The peroxisome proliferator‐activated receptor‐γ (PPARγ) is a ligand‐activated transcription factor belonging to the nuclear receptor superfamily. Peroxisome proliferator‐activated receptor‐γ ligands can inhibit cell growth and increase apoptosis of cancer cell lines, suggesting a potential role for PPARγ as a tumor suppressor. Whereas the related studies between PPARγ and cancer cell invasion are still poor. Our previous study indicates that β‐estradiol (E2) suppresses hepatocellular carcinoma (HCC) cell invasion. We report here that E2 can activate PPARγ of HCC cells, and activated PPARγ suppresses cell invasion by upregulating the expression level of plasminogen activator inhibitor‐1 (PAI‐1). We found that PPARγ plays an important role in the E2‐induced HCC cell invasion process. Using PPARγ agonist GW1929, a reduced invasion effect was found in HCC cell lines, and this inhibition of cell invasion was dosage‐dependent. However, cell invasion was restored by treatment with PPARγ antagonist GW9662. The activated PPARγ upregulated the expression of cell migration‐related protein PAI‐1. Furthermore, knockdown of PPARγ in HCC cells decreased the level of PAI‐1 and advanced cell invasion in response to GW1929. On the contrary, overexpression of PPARγ in HCC cells elevated the level of PAI‐1 and inhibited cell invasion. These findings suggest that PPARγ activation inhibits HCC cell invasion via the upregulation of PAI‐1 and implicate that PPARγ is a target for the treatment and prevention of HCC cell invasion.
机译:过氧化物体增殖物激活的受体-γ(PPARγ)是属于核受体超家族的配体活化转录因子。过氧化物体增殖剂活化受体-γ配体可以抑制细胞生长并增加癌细胞系的凋亡,表明PPARγ作为肿瘤抑制剂的潜在作用。虽然PPARγ和癌细胞侵袭之间的相关研究仍然差。我们以前的研究表明β-雌二醇(E2)抑制肝细胞癌(HCC)细胞侵袭。在此报告E2可以激活HCC细胞的PPARγ,并且通过上调纤溶酶原激活剂抑制剂-1(PAI-1)的表达水平来抑制细胞侵袭的激活PPARγ。我们发现PPARγ在E2诱导的HCC细胞侵入过程中起着重要作用。使用PPARγ激动剂GW1929,在HCC细胞系中发现了降低的侵袭效果,并且这种细胞侵袭的这种抑制是剂量依赖性的。然而,通过用PPARγ拮抗剂GW9662治疗恢复细胞侵袭。活化的PPARγ上调了细胞迁移相关蛋白PAI-1的表达。此外,HCC细胞中PPARγ的敲低降低了PAI-1和高级细胞侵袭的水平,响应于GW1929。相反,HCC细胞中PPARγ的过度表达升高了PAI-1的水平并抑制细胞侵袭。这些发现表明,PPARγ活化通过PAI-1的上调抑制HCC细胞侵袭,并暗示PPARγ是治疗和预防HCC细胞侵袭的靶标。

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