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  4. Alisol B acetate, a triterpene from Alismatis rhizoma, induces Bax nuclear translocation and apoptosis in human hormone-resistant prostate cancer PC-3 cells
 
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Alisol B acetate, a triterpene from Alismatis rhizoma, induces Bax nuclear translocation and apoptosis in human hormone-resistant prostate cancer PC-3 cells

Journal
Cancer Letters
Journal Volume
231
Journal Issue
2
Pages
270-278
Date Issued
2006
Author(s)
Huang Y.-T.
Huang D.-M.
SHIH-CHIEH CHUEH  
Teng C.-M.
JIH-HWA GUH  
DOI
10.1016/j.canlet.2005.02.011
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-29844445293&doi=10.1016%2fj.canlet.2005.02.011&partnerID=40&md5=3023739dd2a286e9b22c79fbbf499206
https://scholars.lib.ntu.edu.tw/handle/123456789/575519
Abstract
The anti-tumor potential of components from Chinese herbal medicines has been greatly concerned. Alisol B acetate, a triterpene from Alismatis rhizoma, induced apoptotic cell death in human hormone-resistant prostate cancer PC-3 cells in a time- and concentration-dependent manner. A good correlation between loss of mitochondrial membrane potential and apoptotic cell death was apparent indicating the participation of mitochondria-related mechanism. Alisol B acetate induced Bax up-regulation and nuclear translocation; it also induced the activation of initiator caspase-8 and caspase-9, and executor caspase-3, suggesting the involvement of both extrinsic and intrinsic apoptosis pathways. Taken together, it is suggested that alisol B acetate induces apoptosis in PC-3 cells via a mitochondria-mediated mechanism with activation of caspase-8, -9 and -3. Furthermore, the Bax activation and translocation from the cytosol to nucleus might be a crucial response to the apoptotic effect. ? 2005 Elsevier Ireland Ltd. All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
alisol b acetate; caspase 3; caspase 8; caspase 9; herbaceous agent; protein Bax; protein bcl 2; triterpene derivative; unclassified drug; Alisma; Alismatis rhizoma; apoptosis; article; cancer cell; cell death; concentration response; controlled study; enzyme activation; hormone resistance; human; human cell; IC 50; membrane potential; mitochondrial membrane; priority journal; prostate cancer; protein expression; upregulation; Alismataceae; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Apoptosis; bcl-2-Associated X Protein; Blotting, Western; Caspases; Cell Nucleus; Cholestenones; Curcumin; Drug Resistance, Neoplasm; Flow Cytometry; Humans; Male; Membrane Potentials; Mitochondria; Neoplasms, Hormone-Dependent; Nitric Oxide Synthase; Paclitaxel; Prostatic Neoplasms; Protein Transport; Proto-Oncogene Proteins c-bcl-2; Triterpenes; Tumor Cells, Cultured; Alisma
Type
journal article

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