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  4. Supercritical carbon dioxide extract of Physalis peruviana induced cell cycle arrest and apoptosis in human lung cancer H661 cells
 
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Supercritical carbon dioxide extract of Physalis peruviana induced cell cycle arrest and apoptosis in human lung cancer H661 cells

Journal
Food and Chemical Toxicology
Journal Volume
47
Journal Volume
47
Journal Issue
6
Journal Issue
6
Pages
1132-1138
Start Page
1132
End Page
1138
ISSN
02786915
Date Issued
2009-06
Author(s)
Wu, Shu-Jing
Chang, Shun-Pang
Lin, Doung-Liang
Wang, Shyh-Shyan
Hou, Fwu-Feuu
LEAN-TEIK HUANG  
DOI
10.1016/j.fct.2009.01.044
URI
https://www.scopus.com/pages/publications/67349115692?inward
http://scholars.lib.ntu.edu.tw/handle/123456789/348404
Abstract
Physalis peruviana L. (PP) is a popular folk medicine used for treating cancer, leukemia, hepatitis, rheumatism and other diseases. In this study, our objectives were to examine the total flavonoid and phenol content of different PP extracts (aqueous: HWEPP; ethanolic: EEPP; supercritical carbon dioxide: SCEPP-0, SCEPP-4 and SCEPP-5) and their antiproliferative effects in human lung cancer H661 cells. Among all the extracts tested, results showed that SCEPP-5 possessed the highest total flavonoid (226.19 ± 4.15 mg/g) and phenol (100.82 ± 6.25 mg/g) contents. SCEPP-5 also demonstrated the most potent inhibitory effect on H661 cell proliferation. Using DNA ladder and flow cytometry analysis, SCEPP-5 effectively induced H661 cell apoptosis as demonstrated by the accumulation of Sub-G1 peak and fragmentation of DNA. SCEPP-5 not only induced cell cycle arrest at S phase, it also up-regulated the expression of pro-apoptotic protein (Bax) and down-regulated the inhibitor of apoptosis protein (IAP). Furthermore, the apoptotic induction in H661 cells was found to associate with an elevated p53 protein expression, cytochrome c release, caspase-3 activation and PARP cleavage. Taken together, these results conclude that SCEPP-5 induced cell cycle arrest at S phase, and its apoptotic induction could be mediated through the p53-dependent pathway and modification of Bax and XIAP proteins expression. The results have also provided important pharmacological backgrounds for the potential use of PP supercritical fluid extract as products for cancer prevention.
Subjects
Apoptosis
Cell cycle arrest
Physalis peruviana
Supercritical carbon dioxide extraction
SDGs

[SDGs]SDG3

Other Subjects
alcohol; carbon dioxide; caspase 3; cytochrome c; DNA; flavonoid; hot water; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase; phenol; Physalis peruviana extract; plant extract; protein Bax; protein p53; unclassified drug; X linked inhibitor of apoptosis; antineoplastic activity; apoptosis; article; cancer cell culture; cancer prevention; cell cycle arrest; cell cycle S phase; concentration response; controlled study; DNA fragmentation; down regulation; drug cytotoxicity; drug effect; drug synthesis; enzyme activation; flow cytometry; human; human cell; lung cancer; Physalis; physalis peruviana; protein cleavage; protein expression; protein secretion; supercritical fluid; supercritical fluid extraction; upregulation; Antineoplastic Agents, Phytogenic; Apoptosis; Blotting, Western; Carbon Dioxide; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Chromatography, Supercritical Fluid; DNA Fragmentation; Flavonoids; Gene Expression Regulation; Humans; Indicators and Reagents; Lung Neoplasms; Phenols; Physalis; Plant Extracts; Physalis peruviana
Type
journal article

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