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Cited 21 times in

BMP-2 promotes oral squamous carcinoma cell invasion by inducing CCL5 release

DC Field Value Language
dc.contributor.author김경남-
dc.contributor.author김광만-
dc.contributor.author김진-
dc.date.accessioned2015-01-06T17:37:26Z-
dc.date.available2015-01-06T17:37:26Z-
dc.date.issued2014-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/100325-
dc.description.abstractBone morphogenetic protein-2 (BMP-2)-containing bone grafts are useful regenerative materials for oral and maxillofacial surgery; however, several in vitro and in vivo studies previously reported cancer progression-related adverse effects caused by BMP-2. In this study, by quantifying the rhBMP-2 content released from bone grafts, the rhBMP-2 concentration that did not show cytotoxicity in each cell line was determined and applied to the in vitro monoculture or coculture model in the invasion assay. Our results showed that 1 ng/ml rhBMP-2, while not affecting cancer cell viability, significantly increased the invasion ability of the cancer cells cocultured with fibroblasts. Cocultured medium with rhBMP-2 also contained increased levels of matrix metalloproteinases. rhBMP-2-treated cocultured fibroblasts did not show a prominent difference in mRNA expression profile. Some cytokines, however, were detected in the conditioned medium by a human cytokine antibody array. Among them, the cancer invasion-related factor CCL5 was quantified by ELISA. Interestingly, CCL5 neutralizing antibodies significantly reduced the invasion of oral cancer cells. In conclusion, our results suggest that 1 ng/ml rhBMP-2 may induce invasion of oral squamous cell carcinoma (OSCC) cells by CCL5 release in coculture models. Therefore, we propose that a careful clinical examination before the use of rhBMP-2-containing biomaterials is indispensable for using rhBMP-2 treatment to prevent cancer progression.-
dc.description.statementOfResponsibilityopen-
dc.format.extent108170-
dc.relation.isPartOfPLOS ONE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHBone Morphogenetic Protein 2/genetics-
dc.subject.MESHBone Morphogenetic Protein 2/metabolism*-
dc.subject.MESHBone Morphogenetic Protein 2/pharmacology-
dc.subject.MESHBone and Bones/metabolism-
dc.subject.MESHCarcinoma, Squamous Cell/genetics-
dc.subject.MESHCarcinoma, Squamous Cell/metabolism*-
dc.subject.MESHCarcinoma, Squamous Cell/pathology*-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Survival/drug effects-
dc.subject.MESHChemokine CCL5/biosynthesis*-
dc.subject.MESHFibroblasts/drug effects-
dc.subject.MESHFibroblasts/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHMatrix Metalloproteinases/metabolism-
dc.subject.MESHMouth Neoplasms/genetics-
dc.subject.MESHMouth Neoplasms/metabolism*-
dc.subject.MESHMouth Neoplasms/pathology*-
dc.subject.MESHNeoplasm Invasiveness-
dc.subject.MESHRecombinant Proteins/pharmacology-
dc.titleBMP-2 promotes oral squamous carcinoma cell invasion by inducing CCL5 release-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Pathology (구강병리학)-
dc.contributor.googleauthorMi-joo Kim-
dc.contributor.googleauthorKwang-mahn Kim-
dc.contributor.googleauthorJin Kim-
dc.contributor.googleauthorKyoung-nam Kim-
dc.identifier.doi10.1371/journal.pone.0108170-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00292-
dc.contributor.localIdA00312-
dc.contributor.localIdA01009-
dc.relation.journalcodeJ02540-
dc.identifier.eissn1932-6203-
dc.identifier.pmid25271422-
dc.contributor.alternativeNameKim, Kyoung Nam-
dc.contributor.alternativeNameKim, Kwang Mahn-
dc.contributor.alternativeNameKim, Jin-
dc.contributor.affiliatedAuthorKim, Kyoung Nam-
dc.contributor.affiliatedAuthorKim, Kwang Mahn-
dc.contributor.affiliatedAuthorKim, Jin-
dc.citation.volume9-
dc.citation.number10-
dc.citation.startPagee108170-
dc.identifier.bibliographicCitationPLOS ONE, Vol.9(10) : e108170, 2014-
dc.identifier.rimsid57590-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Dental Biomaterials and Bioengineering (치과생체재료공학교실) > 1. Journal Papers
2. College of Dentistry (치과대학) > Dept. of Oral Pathology (구강병리학교실) > 1. Journal Papers

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