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dc.contributor.author이영열-
dc.date.accessioned2016-06-07T08:38:05Z-
dc.date.available2016-06-07T08:38:05Z-
dc.date.issued2015-01-
dc.identifier.citationCANCER SCIENCE, v. 106, NO 1, Page. 94-101en_US
dc.identifier.issn1349-7006-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/21551-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1111/cas.12562/full-
dc.description.abstractMetastasis is a challenging clinical problem and the primary cause of death in breast cancer patients. However, there is no therapeutic agent against metastasis of breast cancer cells. Here we report that phloroglucinol, a natural phlorotannin component of brown algae suppresses metastatic ability of breast cancer cells. Treatment with phloroglucinol effectively inhibited mesenchymal phenotypes of basal type breast cancer cells through downregulation of SLUG without causing a cytotoxic effect. Importantly, phloroglucinol decreased SLUG through inhibition of PI3K/AKT and RAS/RAF-1/ERK signaling. In agreement with in vitro data, phloroglucinol was also effective against in vivo metastasis of breast cancer cells, drastically suppressing their metastatic ability to lungs, and extending the survival time of mice. Collectively, our findings demonstrate a novel anticancer activity of phloroglucinol against metastasis of breast cancer cells, implicating its clinical relevance.en_US
dc.description.sponsorshipThis work was supported by the National Research Foundation (NRF) and Ministry of Science, ICT and Future Planning, Korean government, through its National Nuclear Technology Program (NRF-2012M2B2B1055639); and Converging Research Center Program Grant (2013K000283).-
dc.language.isoenen_US
dc.publisherWILEY-BLACKWELLen_US
dc.subjectbasal type breast cancer cellsen_US
dc.subjectcancer metastasisen_US
dc.subjectepithelial-mesenchymal transitionen_US
dc.subjectphloroglucinolen_US
dc.subjectSLUGen_US
dc.titlePhloroglucinol suppresses metastatic ability of breast cancer cells by inhibition of epithelial-mesenchymal cell transitionen_US
dc.typeArticleen_US
dc.relation.no1-
dc.relation.volume106-
dc.identifier.doi10.1111/cas.12562-
dc.relation.page94-101-
dc.relation.journalCANCER SCIENCE-
dc.contributor.googleauthorKim, Rae‐Kwon-
dc.contributor.googleauthorSuh, Yongjoon-
dc.contributor.googleauthorYoo, Ki‐Chun-
dc.contributor.googleauthorCui, Yan‐Hong-
dc.contributor.googleauthorHwang, Eunji-
dc.contributor.googleauthorKim, Hyun‐Jin-
dc.contributor.googleauthorKang, Ju‐Seop-
dc.contributor.googleauthorKim, Min‐Jung-
dc.contributor.googleauthorLee, Young Yiul-
dc.contributor.googleauthorLee, Su‐Jae-
dc.relation.code2015001495-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidleeyy-


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