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[Comparison of transcription factors repressing epithelial phenotype in two different prostate cancer EMT models and its significance].
Wu, Kai-Jie; Zeng, Jin; Zhu, Guo-Dong; Zhang, Dong; Xue, Yan; Chen, Yu-Le; Wang, Xin-Yang; He, Da-Lin.
Afiliação
  • Wu KJ; Department of Urology, The First Affiliated Hospital, Medical School of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China. yidaiwujin@126.com
Zhonghua Nan Ke Xue ; 16(2): 137-41, 2010 Feb.
Article em Zh | MEDLINE | ID: mdl-20369697
ABSTRACT

OBJECTIVE:

To screen and compare the specific transcription factors that repress the epithelial phenotype in epithelial-mesenchymal transition (EMT) in two different human prostate cancer models LNCaP/HIF1alpha and ARCaP.

METHODS:

We established two different prostate cancer EMT models, LNCaP/HIF1alpha and ARCaP, cultured LNCaP, LNCaP/HIF1alpha, IF11 and IA8 cells in vitro, and detected the five transcription factors Snail, Slug, ZEB1, SIP1 and Twist1 in these cells by RT-PCR.

RESULTS:

Different levels of Snail, Slug, ZEB1, SIP1 and Twist1 were detected in both LNCaP and LNCaP/HIF1alpha cells, with significant differences only in the expressions of Slug and Twist1 between the two cells. The expression of Slug was increased, but that of Twist1 decreased in the LNCaP/HIF1alpha cells. All the five transcription factors but Twist1 were expressed in both the IF11 and IA8 cells, but only the express- sions of ZEB1 and Slug were increased significantly in the IA8 cells.

CONCLUSION:

There are different mechanisms underlying transcriptional regulation in different prostate cancer EMT models. Slug may be one of the key transcription factors involved in the HIF1alpha-induced EMT of LNCaP cells, while ZEB1 and Slug may play an important role in repressing the epithelial phenotype of the ARCaP model.
Assuntos
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Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Fatores de Transcrição / Células Estromais Idioma: Zh Ano de publicação: 2010 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Fatores de Transcrição / Células Estromais Idioma: Zh Ano de publicação: 2010 Tipo de documento: Article