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RUNX3 confers sensitivity to pheophorbide a-photodynamic therapy in human oral squamous cell carcinoma cell lines

DC FieldValueLanguage
dc.contributor.author김진-
dc.contributor.author배정윤-
dc.contributor.author배정윤-
dc.date.accessioned2016-02-04T10:59:07Z-
dc.date.available2016-02-04T10:59:07Z-
dc.date.issued2015-
dc.identifier.issn0268-8921-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/139412-
dc.description.abstractPhotodynamic therapy (PDT) with photosensitizer is one of the promising modalities for cancer treatment. For clinical use of PDT, screening process should be preceded to enhance sensitivity to PDT. Thus, we investigated a molecular biomarker to determine the sensitivity to pheophorbide a (Pa)-PDT in immortalized human oral keratinocytes (IHOK) and oral squamous cell carcinoma (OSCC) cell lines. Two IHOK and several OSCC cell lines were used. After Pa-PDT, cell viability was reduced by more than 50%, and reactive oxygen species were generated in IHOK and OSCC cell lines. Additionally, apoptosis occurred in PDT-treated cells. IHOK(S) and IHOK(P), the two IHOK cell lines derived from the same source, showed a difference in cytotoxicity after Pa-PDT. To explain this difference in cytotoxicity, we looked at the expression of Wnt signaling-related genes in these two cell lines, for the morphology of IHOK(S) which was spindle like and elongated and distinct from IHOK(P) and the parent cell. Among the relevant genes, runt-related transcription factor 3 (RUNX3), an apoptosis-related gene, was selected as a potential marker that confers sensitivity to PDT. We found that the cytotoxicity by Pa-PDT was proportional to RUNX3 expression in OSCC cell lines. Additionally, knockdown of RUNX3 expression reduced cytotoxicity by Pa-PDT, suggesting that RUNX3 might be a biomarker to determine sensitivity to Pa-PDT. This was the first study to find a new target molecule that enhances Pa-PDT effects in IHOK and OSCC cell lines. Hence, the development of a PDT-dependent biomarker could provide a novel approach to improve the effects of PDT on oral precancerous and cancerous lesions.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfLASERS IN MEDICAL SCIENCE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHApoptosis/drug effects-
dc.subject.MESHCarcinoma, Squamous Cell/metabolism-
dc.subject.MESHCarcinoma, Squamous Cell/therapy*-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHChlorophyll/analogs & derivatives*-
dc.subject.MESHChlorophyll/chemistry-
dc.subject.MESHCore Binding Factor Alpha 3 Subunit/physiology*-
dc.subject.MESHGene Expression Regulation, Neoplastic-
dc.subject.MESHHumans-
dc.subject.MESHKeratinocytes/metabolism-
dc.subject.MESHMouth Neoplasms/metabolism-
dc.subject.MESHMouth Neoplasms/therapy*-
dc.subject.MESHPhotochemotherapy/methods*-
dc.subject.MESHPhotosensitizing Agents/therapeutic use-
dc.subject.MESHReactive Oxygen Species/metabolism-
dc.subject.MESHSignal Transduction-
dc.subject.MESHWnt Proteins/metabolism-
dc.titleRUNX3 confers sensitivity to pheophorbide a-photodynamic therapy in human oral squamous cell carcinoma cell lines-
dc.typeArticle-
dc.contributor.collegeResearcher Institutes (부설 연구소)-
dc.contributor.departmentOral Cancer Research Institute (구강종양연구소)-
dc.contributor.googleauthorSook Moon-
dc.contributor.googleauthorJung Yoon Bae-
dc.contributor.googleauthorHwa-Kyung Son-
dc.contributor.googleauthorDoo Young Lee-
dc.contributor.googleauthorGyeongju Park-
dc.contributor.googleauthorHyun You-
dc.contributor.googleauthorHyojin Ko-
dc.contributor.googleauthorYong-Chul Kim-
dc.contributor.googleauthorJin Kim-
dc.identifier.doi10.1007/s10103-013-1350-1-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01009-
dc.relation.journalcodeJ02158-
dc.identifier.eissn1435-604X-
dc.identifier.pmid23700080-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs10103-013-1350-1-
dc.subject.keywordPhotodynamic therapy-
dc.subject.keywordPheophorbide a-
dc.subject.keywordOral squamous cell carcinoma-
dc.subject.keywordImmortalized human oral keratinocytes-
dc.subject.keywordRUNX3-
dc.contributor.alternativeNameKim, Jin-
dc.contributor.alternativeNameBae, Jung Yoon-
dc.contributor.affiliatedAuthorKim, Jin-
dc.rights.accessRightsnot free-
dc.citation.volume30-
dc.citation.number2-
dc.citation.startPage499-
dc.citation.endPage507-
dc.identifier.bibliographicCitationLASERS IN MEDICAL SCIENCE, Vol.30(2) : 499-507, 2015-
Appears in Collections:
5. Research Institutes (연구소) > Oral Cancer Research Institute (구강종양연구소) > 1. Journal Papers
2. College of Dentistry (치과대학) > Dept. of Oral Pathology (구강병리학교실) > 1. Journal Papers

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