Obovatol inhibits colorectal cancer growth by inhibiting tumor cell proliferation and inducing apoptosis = 오보바톨의 항암효과

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dc.contributor.authorSu Kyung Lee-
dc.contributor.authorHye Nan Kim-
dc.contributor.authorYeong-Rim Kang-
dc.contributor.authorChang Woo Lee-
dc.contributor.authorHwan Mook Kim-
dc.contributor.authorDong Cho Han-
dc.contributor.authorJ Shin-
dc.contributor.authorK Bae-
dc.contributor.authorByoung-Mog Kwon-
dc.date.accessioned2017-04-19T09:11:41Z-
dc.date.available2017-04-19T09:11:41Z-
dc.date.issued2008-
dc.identifier.issn0968-0896-
dc.identifier.uri10.1016/j.bmc.2008.08.033ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8587-
dc.description.abstractNeolignans such as obovatol, honokiol, and magnolol have been previously reported to show various biological activities including anti-inflammation and antitumor effects. This is the first demonstration on the in vivo antitumor effect of obovatol on human colorectal carcinoma SW620 cells. Nude mice were implanted with SW620 cells and fed with vehicle or 5 mg/kg/d dose of obovatol for 20 days. Obovatol inhibited tumor growth that accounted for 50% decrease in tumor volume and 44.6% decrease in tumor weight at the end of the experiment without any adverse health effect. In nude mice bearing SW620-incubated tumor, obovatol exhibited more potent antitumor activity than honolkiol. In addition, DNA flow cytometric analysis shows that obovatol progresses to apoptosis as detected by flow cytometry after double staining with annexin V and propidium iodide. Thus, we suggest that obovatol is a potent inducer of cell apoptosis in SW620 cells, and a potent antitumor agent.-
dc.publisherElsevier-
dc.titleObovatol inhibits colorectal cancer growth by inhibiting tumor cell proliferation and inducing apoptosis = 오보바톨의 항암효과-
dc.title.alternativeObovatol inhibits colorectal cancer growth by inhibiting tumor cell proliferation and inducing apoptosis-
dc.typeArticle-
dc.citation.titleBioorganic & Medicinal Chemistry-
dc.citation.number17-
dc.citation.endPage8402-
dc.citation.startPage8397-
dc.citation.volume16-
dc.contributor.affiliatedAuthorSu Kyung Lee-
dc.contributor.affiliatedAuthorHye Nan Kim-
dc.contributor.affiliatedAuthorYeong-Rim Kang-
dc.contributor.affiliatedAuthorChang Woo Lee-
dc.contributor.affiliatedAuthorHwan Mook Kim-
dc.contributor.affiliatedAuthorDong Cho Han-
dc.contributor.affiliatedAuthorByoung-Mog Kwon-
dc.contributor.alternativeName이수경-
dc.contributor.alternativeName김혜난-
dc.contributor.alternativeName강영림-
dc.contributor.alternativeName이창우-
dc.contributor.alternativeName김환묵-
dc.contributor.alternativeName한동초-
dc.contributor.alternativeName신종헌-
dc.contributor.alternativeName배기환-
dc.contributor.alternativeName권병목-
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry, vol. 16, no. 17, pp. 8397-8402-
dc.identifier.doi10.1016/j.bmc.2008.08.033-
dc.subject.keywordAntitumor-
dc.subject.keywordApoptosis-
dc.subject.keywordHonokiol-
dc.subject.keywordMagnolia obovata Thunb-
dc.subject.keywordObovatol-
dc.subject.localAnti-tumor-
dc.subject.localantitumor-
dc.subject.localAntitumor-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localhonokiol-
dc.subject.localHonokiol-
dc.subject.localMagnolia obovata THUNB-
dc.subject.localMagnolia obovata Thunb-
dc.subject.localobovatol-
dc.subject.localObovatol-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
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