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Protein expression pattern in response to ionizing radiation in MCF-7 human breast cancer cells

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dc.contributor.authorJung, Samil-
dc.contributor.authorLee, Soonduck-
dc.contributor.authorLee, Jayhee-
dc.contributor.authorLi, Chengping-
dc.contributor.authorOhk, Ji-Yeon-
dc.contributor.authorJeong, Hyeon-Kyung-
dc.contributor.authorLee, Seungkyu-
dc.contributor.authorKim, Sangwoo-
dc.contributor.authorChoi, Yunyeong-
dc.contributor.authorKim, Sunghak-
dc.contributor.authorLee, Heungwoo-
dc.contributor.authorLee, Myeong-Sok-
dc.date.available2021-02-22T12:47:24Z-
dc.date.issued2012-01-
dc.identifier.issn1792-1074-
dc.identifier.issn1792-1082-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/12002-
dc.description.abstractBreast cancer is one of the most common types of cancer in women and is highly treatable by radiotherapy. However, repeated exposure to radiation results in tumor cell resistance. Understanding the molecular mechanisms involved in the response of tumors to gamma-irradiation is important for improving radiotherapy. For this reason, we aimed to identify radiation-responsive genes at the protein level. In the present study, we observed differentially expressed proteins using 2D-PAGE and MALDI-TOF-MS for the global analysis of protein expression patterns in response to ionizing radiation (IR). When the expression patterns of proteins were compared to a control gel, numerous spots were found that differed greatly. Among them, 11 spots were found to be significantly different. One set of proteins (GH2, RGS17, BAK1, CCNH, TSG6, RAD51B, IGFBP1 and CASP14) was upregulated and another set of proteins (C1QRF, PLSCR2 and p34(SEI-1)) was downregulated after exposure to gamma-rays. These proteins are known to be related to cell cycle control, apoptosis, DNA repair, cell proliferation and other signaling pathways.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherSPANDIDOS PUBL LTD-
dc.titleProtein expression pattern in response to ionizing radiation in MCF-7 human breast cancer cells-
dc.typeArticle-
dc.publisher.location그리이스-
dc.identifier.doi10.3892/ol.2011.444-
dc.identifier.scopusid2-s2.0-84855249727-
dc.identifier.wosid000298124700027-
dc.identifier.bibliographicCitationONCOLOGY LETTERS, v.3, no.1, pp 147 - 154-
dc.citation.titleONCOLOGY LETTERS-
dc.citation.volume3-
dc.citation.number1-
dc.citation.startPage147-
dc.citation.endPage154-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusBCL-2 HOMOLOG BAK-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusBINDING-PROTEINS-
dc.subject.keywordPlusCYCLE REGULATION-
dc.subject.keywordPlusLUNG-CANCER-
dc.subject.keywordPlusHEPATITIS-B-
dc.subject.keywordPlusP53-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordAuthorbreast cancer-
dc.subject.keywordAuthorionizing radiation-
dc.subject.keywordAuthor2D-PAGE-
dc.identifier.urlhttps://www.spandidos-publications.com/10.3892/ol.2011.444-
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