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자료유형
학술저널
저자정보
Wang, Li-Meng (Liaoning Provincial Key Laboratory of Biotechnology and Drug Discover, College of Life Science, Liaoning Normal University) Xie, Kun-Peng (Liaoning Provincial Key Laboratory of Biotechnology and Drug Discover, College of Life Science, Liaoning Normal University) Huo, Hong-Nan (Liaoning Provincial Key Laboratory of Biotechnology and Drug Discover, College of Life Science, Liaoning Normal University) Shang, Fei (Liaoning Provincial Key Laboratory of Biotechnology and Drug Discover, College of Life Science, Liaoning Normal University) Zou, Wei (Liaoning Provincial Key Laboratory of Biotechnology and Drug Discover, College of Life Science, Liaoning Normal University) Xie, Ming-Jie (Liaoning Provincial Key Laboratory of Biotechnology and Drug Discover, College of Life Science, Liaoning Normal University)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제13권 제4호
발행연도
2012.1
수록면
1,431 - 1,437 (7page)

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The growth of many breast tumors is stimulated by IGF-1, which activates signal transduction pathways inducing cell proliferation. $ER{\alpha}$ is important in this process. The aim of the study was to investigate relationships in vitro among inhibitory effects of luteolin on the growth of MCF-7 cells, IGF-1 pathway and $ER{\alpha}$. Our results showed that luteolin could effectively block IGF-l-stimulated MCF-7 cell proliferation in a dose- and time-dependent manner and block cell cycle progression and induce apoptosis evidenced by the flow cytometric detection of sub-G1DNA content. Luteolin markedly decreased IGF-l-dependent IGF-IR and Akt phosphorylation without affecting Erk1/2 phosphorylation. Further experiments pointed out that $ER{\alpha}$ was directly involved in IGF-l induced cell growth inhibitory effects of luteolin, which significantly decreased $ER{\alpha}$ expression. Knockdown of $ER{\alpha}$ in MCF-7 cells by an $ER{\alpha}$-specific siRNA decreased the IGF-l induced cell growth inhibitory effects of luteolin. $ER{\alpha}$ is thus a possible target of luteolin. These findings indicate that the inhibitory effect of luteolin on the growth of MCF-7 cells is via inhibiting IGF-l mediated PI3K-Akt pathway dependent of $ER{\alpha}$ expression.

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