Takano Shinichi, Kanai Fumihiko, Jazag Amarsanaa, Ijichi Hideaki, Yao Jian, Ogawa Hideoki, Enomoto Nobuyuki, Omata Masao, Nakao Atsuhito
Department of Immunology, University of Yamanashi, Yamanashi 409-3898, Japan.
J Biochem. 2007 Mar;141(3):345-51. doi: 10.1093/jb/mvm039. Epub 2007 Feb 14.
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.
Smad4是一种在胰腺癌中经常缺失的肿瘤抑制基因。为了研究Smad4缺陷在胰腺癌侵袭和转移能力中的作用,我们检测了Smad4缺陷对胰腺癌细胞系PANC-1中侵袭抑制因子E-钙黏蛋白调控的影响。转化生长因子-β(TGF-β)降低了质膜上E-钙黏蛋白和β-连环蛋白的表达,增加了Snail和Slug信使核糖核酸的表达,并诱导PANC-1细胞出现成纤维细胞样形态。在敲低Smad4的PANC-1细胞中,TGF-β的这些作用被消除。我们还发现,在敲低Snail和Slug的PANC-1细胞中,TGF-β诱导的E-钙黏蛋白表达下调受到部分抑制。因此,Smad4至少部分地通过诱导Snail和Slug介导TGF-β诱导的PANC-1细胞中E-钙黏蛋白的下调。这些结果表明,在侵袭性和转移性胰腺癌中观察到的Smad4缺陷可能与E-钙黏蛋白的缺失无关。