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자료유형
학술저널
저자정보
Lee, Kyung-Ae (Department of Biochemistry, College of Medicine, Soonchunhyang University) Lee, Sang-Han (Department of Biochemistry, College of Medicine, Soonchunhyang University) Lee, Yong-Jin (Soonchunhyung Environmental Health Center for Asbestos-Related Disease, College of Medicine, Soonchunhyang University Cheonan Hospital) Baeg, Seung-Mi (Department of Biochemistry, College of Medicine, Soonchunhyang University) Shim, Jung-Hyun (Department of Biochemistry, College of Medicine, Soonchunhyang University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제20권 제3호
발행연도
2012.1
수록면
273 - 279 (7page)

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Hesperidin, a flavanone present in citrus fruits, has been studied as potential therapeutic agents that have anti-tumor activity and apoptotic effects in several cancers, but there is no report about the apoptotic effect of hesperidin in human malignant pleural mesothelioma through the specificity protein 1 (Sp1) protein. We investigated whether hesperidin inhibited cell growth and regulated Sp1 target proteins by suppressing the levels of Sp1 protein in MSTO-211H cells. The $IC_{50}$ value of hesperidin was determined to be 152.3 ${\mu}M$ in MSTO-211H cells for 48 h. Our results suggested that hesperidin (0-160 ${\mu}M$) decreased cell viability, and induced apoptotic cell death. Hesperidin increased Sub-$G_1$ population in MSTO-211H cells. Hesperidin significantly suppressed mRNA/protein level of Sp1 and modulated the expression level of the Sp1 regulatory protein such as p27, p21, cyclin D1, Mcl-1, and survivin in mesothelioma cells. Also, hesperidin induced apoptotic signaling including: cleavages of Bid, caspase-3, and PARP, upregulation of Bax, and down-regulation of Bcl-$_{xl}$ in mesothelioma cells. These results show that hesperidin suppressed mesothelioma cell growth through inhibition of Sp1. In this study, we demonstrated that Sp1 acts as a novel molecular target of hesperidin in human malignant pleural mesothelioma.

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