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Kaempferol and quercetin, components of Ginkgo biloba extract (EGb 761), induce caspase-3-dependent apoptosis in oral cavity cancer cells

Authors
 Ju Wan Kang  ;  Jeong Hong Kim  ;  Keejae Song  ;  Si Hong Kim  ;  Joo-Heon Yoon  ;  Kyung-Su Kim 
Citation
 PHYTOTHERAPY RESEARCH, Vol.24(suppl 1) : 77-82, 2010 
Journal Title
 PHYTOTHERAPY RESEARCH 
ISSN
 0951-418X 
Issue Date
2010
MeSH
Antineoplastic Agents, Phytogenic/pharmacology ; Apoptosis/drug effects* ; Caspase 3/metabolism* ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Ginkgo biloba/chemistry ; Humans ; Kaempferols/pharmacology* ; Mouth Neoplasms/metabolism* ; Plant Extracts/pharmacology* ; Quercetin/pharmacology*
Keywords
Ginkgo biloba extract ; oral cavity cancer ; apoptosis ; caspase-3
Abstract
EGb 761, extracted from Ginkgo biloba leaves, has been proven to induce caspase-3-dependent apoptosis in oral cavity cancer cells. Since EGb 761 is a composition of various components, it is important to identify which components are responsible for its anticancer effects to reduce the total dosage and to avoid toxicity. Therefore, the study aimed to determine the effective compounds of EGb 761 that induce apoptosis in oral cavity cancer cells and to identify whether caspase-3 was involved in apoptosis of oral cancer cells by EGb 761 components. The results of cell proliferation assays on oral cavity cancer cells showed that kaempferol and quercetin significantly inhibited cellular proliferation at a concentration of 40 microM. Flow cytometry showed that the antiproliferative effects of each component were due to increased apoptosis. Kaempferol and quercetin induced apoptosis in various oral cancer cell lines (SCC-1483, SCC-25 and SCC-QLL1) and showed cleavage of poly (ADP-ribose) polymerase (PARP). Caspase-3 activity assay revealed that induction of apoptosis by kaempferol and quercetin was caspase-3-dependent. In conclusion, the results suggest that kaempferol and quercetin, two components of EGb 761, effectively induce caspase-3-dependent apoptosis of oral cavity cancer cells and can be considered as possible anti-oral cavity cancer agents.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/ptr.2913/abstract
DOI
10.1002/ptr.2913
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
Yonsei Authors
Kang, Ju Wan(강주완)
Kim, Kyung Su(김경수) ORCID logo https://orcid.org/0000-0003-1460-0640
Yoon, Joo Heon(윤주헌)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/101395
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