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Down-regulation of Gli-1 inhibits hepatocellular carcinoma cell migration and invasion.
Chen, Jing-Song; Li, Hua-Shu; Huang, Jiong-Qiang; Zhang, Long-Juan; Chen, Xi-Lin; Wang, Qian; Lei, Jian; Feng, Ju-Tao; Liu, Qin; Huang, Xiao-Hui.
Afiliação
  • Chen JS; Department of Gastrointesinal Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, People's Republic of China, hychenjs@126.com.
Mol Cell Biochem ; 393(1-2): 283-91, 2014 Aug.
Article em En | MEDLINE | ID: mdl-24792036
ABSTRACT
Glioma-associated oncogene homolog-1 (Gli-1) is considered a marker of Hedgehog pathway activation and is associated with the progression of several cancers. We have previously reported that Gli-1 was correlated with invasion and metastasis in hepatocellular carcinoma (HCC). However, the exact roles and mechanisms of Gli-1 in HCC invasion are unclear. In this study, we found that small interfering RNA mediated down-regulation of Gli-1 expression significantly suppressed adhesion, motility, migration, and invasion of both SMMC-7721 and SK-Hep1 cells. Furthermore, down-regulation of Gli-1 significantly reduced expressions and activities of both matrix metalloproteinase (MMP)-2 and MMP-9. In addition, we found that down-regulation of Gli-1 resulted in up-regulation of E-cadherin and concomitant down-regulation of Snail and Vimentin, consistent with inhibition of epithelial-mesenchymal transition (EMT). Taken together, our results suggest that down-regulation of Gli-1 suppresses HCC cell migration and invasion likely through inhibiting expressions and activations of MMP-2, 9 and blocking EMT.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Movimento Celular / Carcinoma Hepatocelular / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: Mol Cell Biochem Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Movimento Celular / Carcinoma Hepatocelular / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: Mol Cell Biochem Ano de publicação: 2014 Tipo de documento: Article