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Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity.

Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Research Abstract Details 

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  • Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Abstract Text:

    yang huYang Hu,yong yangYong Yang,qi-dong youQi-Dong You,wei liuWei Liu,hong-yan guHong-Yan Gu,li zhaoLi Zhao,kun zhangKun Zhang,wei wangWei Wang,xiao-tang wangXiao-Tang Wang,qing-long guoQing-Long Guo,

    We previously reported that wogonin, a flavonoid compound, was a potent apoptosis inducer of human hepatoma SMMC-7721 cells and murine sarcoma S180 cells. In the present study, the effect of oroxylin A, one wogonin structurally related flavonoid isolated from Scutellariae radix, on human hepatocellular carcinoma cell line HepG2 was examined and molecular mechanisms were also investigated. Oroxylin A inhibited HepG2 cell proliferation in a concentration- and time-dependent manner measured by MTT-assay. Treatment with an apoptosis-inducing concentration of oroxylin A caused typical morphological changes and apoptotic blebbing in HepG2 cells. DNA fragmentation assay was used to examine later apoptosis induced by oroxylin A. FACScan analysis revealed a dramatic increase in the number of apoptotic and G(2)/M phase arrest cells after oroxylin A treatment. The pro-apoptotic activity of oroxylin A was attributed to its ability to modulate the concerted expression of Bcl-2, Bax, and pro-caspase-3 proteins. The expression of Bcl-2 protein and pro-caspase-3 protein was dramatically decreased after treatment with oroxylin A. These results demonstrated that oroxylin A could effectively induce programmed cell death and suggested that it could be a promising antitumor drug.

    Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Publishing Authors By Initials

    y huY Hu,y yangY Yang,qd youQD You,w liuW Liu,hy guHY Gu,l zhaoL Zhao,k zhangK Zhang,w wangW Wang,xt wangXT Wang,ql guoQL Guo,

    For similar peptides: intracellular signaling peptides and proteins: apoptosis regulatory proteins: proto-oncogene proteins c-bcl-2: bcl-2-associated x protein research abstracts see: peptides: intracellular signaling peptides and proteins: apoptosis regulatory proteins: proto-oncogene proteins c-bcl-2: bcl-2-associated x protein research

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    Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Biochemical and biophysical research communication

    VOLUME: 351

    Page Numbers: 521-7

    Journal Abbreviation: Biochem. Biophys. Res. Commun.

    ISSN: 0006-291X

    DAY: 19

    MONTH: 10

    YEAR: 2006

    Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 372516

    Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Keywords Mesh Terms:

    KEYWORDS: bcl-2-Associated X Protein

    MESH TERMS: biosynthesis

    Chemical & Substance for Abstract: Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity. Information

    Substance Name: Caspase 3

    Registry Number: EC 3.4.22.-

    Grant and Affiliation Information for Oroxylin A induced apoptosis of human hepatocellular carcinoma cell line HepG2 was involved in its antitumor activity.

    AFFILIATION: Department of Physiology, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: S06GM-008205

    ACRONYM: GM

    MEDLINETA: Biochem Biophys Res Commun

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