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Astrocyte elevated gene-1 induces breast cancer proliferation and invasion through upregulating HER2/neu expression / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 3546-3550, 2011.
Article de En | WPRIM | ID: wpr-336530
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>BACKGROUND</b>Astrocyte elevated gene-1 (AEG-1), primarily identified as a late response gene induced by HIV-1 infection, plays multiple roles in the process of oncogenesis. This novel gene has been demonstrated to be involved in the several potent carcinogenic pathways, including PI3K/Akt pathway, nuclear factor (NF)-κB pathway, and Wnt/κ-catenin pathway. Although the function of AEG-1 has been intensively investigated in recent years, the molecular mechanism underlying its oncogenic role is largely unknown. The aim of this research was to explore the potential function of AEG-1 in breast cancer development and progression.</p><p><b>METHODS</b>AEG-1 was ectopically overexpressed in breast cancer MCF-7 cells and its biological effects on the proliferation and invasion of MCF-7 cells were studied by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and invasion assays. The expression of HER2/neu, a crucial oncogene involving in breast cancer carcinogenesis, was also determined.</p><p><b>RESULTS</b>Overexpression of the AEG-1 promoted the proliferation and invasion ability of breast cancer cells, and upregulated the expression of HER2/neu, a crucial oncogene involving in breast cancer carcinogenesis.</p><p><b>CONCLUSION</b>AEG-1 might facilitate the proliferation and invasion of breast cancer cells by upregulating HER2/neu expression, which provides a potential target for breast cancer therapy.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Physiologie / Tumeurs du sein / Transduction du signal / Molécules d&apos;adhérence cellulaire / Survie cellulaire / Technique de Western / Récepteur ErbB-2 / Lignée cellulaire tumorale / Prolifération cellulaire / Réaction de polymérisation en chaine en temps réel Type d'étude: Prognostic_studies Limites du sujet: Humans langue: En Texte intégral: Chinese Medical Journal Année: 2011 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Physiologie / Tumeurs du sein / Transduction du signal / Molécules d&apos;adhérence cellulaire / Survie cellulaire / Technique de Western / Récepteur ErbB-2 / Lignée cellulaire tumorale / Prolifération cellulaire / Réaction de polymérisation en chaine en temps réel Type d'étude: Prognostic_studies Limites du sujet: Humans langue: En Texte intégral: Chinese Medical Journal Année: 2011 Type: Article