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DOI: 10.1055/s-2007-993739
© Georg Thieme Verlag KG Stuttgart · New York
Secoaggregatalactone-A from Lindera aggregata Induces Apoptosis in Human Hepatoma Hep G2 Cells
Publication History
Received: May 26, 2007
Revised: October 5, 2007
Accepted: October 15, 2007
Publication Date:
12 November 2007 (online)
Abstract
A new secobutanolide, secoaggregatalactone A (1) was isolated from the leaves of Lindera aggregata. Results obtained from the cytotoxicity assay revealed that secoaggregatalactone A exhibited a noticeable cytotoxicity (EC50 = 6.61 μg/mL; 22.1 μM) against the human hepatoma cell line (Hep G2 cell line). According to morphological observations, flow cytometric analysis, and DNA fragmentation analysis, it was proven that the cytotoxicity of secoaggregatalactone A on human cells was due to apoptosis. Moreover, based on the results from the protein expression assay and confocal laser scanning microscope observations, it is assumed that secoaggregatalactone A induced apoptosis through the mitochondria pathway by way of cleavage of Bit to release cytochrome C and activate caspases-9 and -3, and then degradation of PARP.
Key words
Secoaggregatalactone A - apoptosis - cytotoxicity - Lindera aggregata - Lauraceae - mitochondrial pathway
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- Supporting Information .
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Dr. Sheng-Yang Wang
Department of Forestry
National Chung-Hsing University
250 Kuo-Kuang Road
Taichung 402
Taiwan
R.O.C.
Phone: +886-4-2284-0345 ext. 138
Fax: +886-4-2287-3628.
Email: taiwanfir@dragon.nchu.edu.tw
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