首页> 外文期刊>The Journal of Biochemistry >Smad4 is essential for down-regulation of E-cadherin induced by TGF-beta in pancreatic cancer cell line PANC-1.
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Smad4 is essential for down-regulation of E-cadherin induced by TGF-beta in pancreatic cancer cell line PANC-1.

机译:Smad4对于下调胰腺癌细胞系PANC-1中TGF-β诱导的E-钙粘着蛋白至关重要。

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摘要

Smad4 is a tumour suppressor gene frequently deleted in pancreatic cancer. To investigate the roles of Smad4 deficiency in invasive and matastatic capabilities of pancreatic cancer, we examined the effects of Smad4 deficiency on regulation of the invasion suppressor E-cadherin in pancreatic cancer cell line PANC-1. TGF-beta decreased expression of E-cadherin and beta-catenin proteins at the plasma membrane, increased Snail and Slug mRNA expression, and induced fibroblastoid morphology in PANC-1 cells. These effects of TGF-beta were abrogated in Smad4-knocked-down PANC-1 cells. We also found that TGF-beta-induced down-regulation of E-cadherin expression was partially inhibited in Snail- and Slug-knocked-down PANC-1 cells. Thus, Smad4 mediates down-regulation of E-cadherin induced by TGF-beta in PANC-1 cells, at least in part, through Snail and Slug induction. These results suggest that Smad4 deficiency observed in invasive and metastatic pancreatic cancer might not be linked to the loss of E-cadherin.
机译:Smad4是在胰腺癌中经常缺失的肿瘤抑制基因。为了研究Smad4缺乏在胰腺癌的侵袭和成熟能力中的作用,我们检查了Smad4缺乏对胰腺癌细胞株PANC-1中侵袭抑制因子E-钙粘蛋白调节的影响。 TGF-β降低了质膜上E-cadherin和β-catenin蛋白的表达,增加了Snail和Slug mRNA的表达,并诱导了PANC-1细胞中的成纤维细胞形态。在Smad4敲低的PANC-1细胞中,TGF-β的这些作用被取消。我们还发现,在Snail和Slug基因敲低的PANC-1细胞中,TGF-β诱导的E-钙粘蛋白表达下调被部分抑制。因此,Smad4至少部分地通过Snail和Slug诱导介导了PANC-1细胞中TGF-β诱导的E-钙粘蛋白的下调。这些结果表明,在浸润性和转移性胰腺癌中观察到的Smad4缺乏症可能与E-钙粘蛋白的丢失无关。

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