Dehydrotrametenolic acid selectively inhibits the growth of H-ras transformed rat2 cells and induces apoptosis through caspase-3 pathway = Dehydrotrametenolic acid의 세포사멸 유도를 통한 항암효과

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dc.contributor.authorHyun-Mi Kang-
dc.contributor.authorSu-Kyung Lee-
dc.contributor.authorDae Seop Shin-
dc.contributor.authorMi-Young Lee-
dc.contributor.authorDong Cho Han-
dc.contributor.authorN I Baek-
dc.contributor.authorKwang Hee Son-
dc.contributor.authorByoung-Mog Kwon-
dc.date.accessioned2017-04-19T09:03:54Z-
dc.date.available2017-04-19T09:03:54Z-
dc.date.issued2006-
dc.identifier.issn0024-3205-
dc.identifier.uri10.1016/j.lfs.2005.05.066ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7231-
dc.description.abstractThe screening of natural products that preferentially inhibit growth of H-ras transformed rat2 cells vs. rat2 cells was performed to identify H-ras specific growth inhibitor. A lanostane-type triterpene acid, dehydrotrametenolic acid (3β-hydroxylanosta-7,9(11),24-trien-21-oic acid), was isolated from the sclerotium of Poria cocos (Polyporaceae). Dehydrotrametenolic acid selectively inhibited the growth of H-ras transformed cells with a GI 50 value of 40 μM. FACS analysis indicated that the compound exerted its anti-proliferation effects through cell cycle arrest at G2/M phase and accumulation of sub-G1 population. Dehydrotrametenolic acid-induced apoptosis was further confirmed with chromosomal DNA fragmentation, caspase-3 activation, and degradation of PARP and Lamin A/C degradation. The compound also regulated the expression of H-ras, Akt and Erk, which are the downstream proteins of H-ras signaling pathways. The results suggest that dehydrotrametenolic acid can be a potential anticancer agent against H-ras transformed tumor.-
dc.publisherElsevier-
dc.titleDehydrotrametenolic acid selectively inhibits the growth of H-ras transformed rat2 cells and induces apoptosis through caspase-3 pathway = Dehydrotrametenolic acid의 세포사멸 유도를 통한 항암효과-
dc.title.alternativeDehydrotrametenolic acid selectively inhibits the growth of H-ras transformed rat2 cells and induces apoptosis through caspase-3 pathway-
dc.typeArticle-
dc.citation.titleLife Sciences-
dc.citation.number6-
dc.citation.endPage613-
dc.citation.startPage607-
dc.citation.volume78-
dc.contributor.affiliatedAuthorHyun-Mi Kang-
dc.contributor.affiliatedAuthorSu-Kyung Lee-
dc.contributor.affiliatedAuthorDae Seop Shin-
dc.contributor.affiliatedAuthorMi-Young Lee-
dc.contributor.affiliatedAuthorDong Cho Han-
dc.contributor.affiliatedAuthorKwang Hee Son-
dc.contributor.affiliatedAuthorByoung-Mog Kwon-
dc.contributor.alternativeName강현미-
dc.contributor.alternativeName이수경-
dc.contributor.alternativeName신대섭-
dc.contributor.alternativeName이미영-
dc.contributor.alternativeName한동초-
dc.contributor.alternativeName백남인-
dc.contributor.alternativeName손광희-
dc.contributor.alternativeName권병목-
dc.identifier.bibliographicCitationLife Sciences, vol. 78, no. 6, pp. 607-613-
dc.identifier.doi10.1016/j.lfs.2005.05.066-
dc.subject.keywordApoptosis-
dc.subject.keywordCaspase-3-
dc.subject.keywordCell cycle arrest-
dc.subject.keywordDehydrotrametenolic acid-
dc.subject.keywordH-ras-
dc.subject.keywordPoria cocos Wolf-
dc.subject.localApoptosis-
dc.subject.localapoptosis-
dc.subject.localCaspase 3-
dc.subject.localCaspase-3-
dc.subject.localcaspase-3-
dc.subject.localCell cycle arrest-
dc.subject.localcell cycle arrest-
dc.subject.localDehydrotrametenolic acid-
dc.subject.localH-Ras-
dc.subject.localH-ras-
dc.subject.localPoria cocos Wolf-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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