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RASSF1A suppresses the activated K-Ras-induced oxidative DNA damage

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dc.contributor.authorPark, Seon Ho-
dc.contributor.authorKim, Jung Jin-
dc.contributor.authorChung, Jin Sil-
dc.contributor.authorLee, So Ra-
dc.contributor.authorLee, Gi Young-
dc.contributor.authorKim, Hyung Jung-
dc.contributor.authorDo Yoo, Young-
dc.date.accessioned2021-09-07T13:06:08Z-
dc.date.available2021-09-07T13:06:08Z-
dc.date.created2021-06-14-
dc.date.issued2011-04-29-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/112623-
dc.description.abstractThe mutant K-Ras elevates intracellular reactive oxygen species (ROS) levels and leads to oxidative DNA damage, resulting in malignant cell transformation. Ras association domain family 1 isoform A (RASSF1A) is known to play a role as a Ras effector. However, the suppressive effect of RASSF1A on K-RasV12-induced ROS increase and DNA damage has not been identified. Here, we show that RASSF1A blocks K-RasV12-triggered ROS production. RASSF1A expression also inhibits oxidative DNA damage and chromosomal damage. From the results obtained in this study, we suggest that RASSF1A regulates the cellular ROS levels enhanced by the Ras signaling pathway, and that it may function as a tumor suppressor by suppressing DNA damage caused by activated Ras. (C) 2011 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectCELL-CYCLE PROGRESSION-
dc.subjectTUMOR-SUPPRESSOR-
dc.subjectEPIGENETIC INACTIVATION-
dc.subjectROS PRODUCTION-
dc.subjectLUNG-
dc.subjectFIBROBLASTS-
dc.subjectSUPEROXIDE-
dc.subjectGENERATION-
dc.subjectPROTEIN-
dc.subjectROMO1-
dc.titleRASSF1A suppresses the activated K-Ras-induced oxidative DNA damage-
dc.typeArticle-
dc.contributor.affiliatedAuthorDo Yoo, Young-
dc.identifier.doi10.1016/j.bbrc.2011.03.139-
dc.identifier.scopusid2-s2.0-79955374780-
dc.identifier.wosid000290781000026-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.408, no.1, pp.149 - 153-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume408-
dc.citation.number1-
dc.citation.startPage149-
dc.citation.endPage153-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusCELL-CYCLE PROGRESSION-
dc.subject.keywordPlusTUMOR-SUPPRESSOR-
dc.subject.keywordPlusEPIGENETIC INACTIVATION-
dc.subject.keywordPlusROS PRODUCTION-
dc.subject.keywordPlusLUNG-
dc.subject.keywordPlusFIBROBLASTS-
dc.subject.keywordPlusSUPEROXIDE-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusROMO1-
dc.subject.keywordAuthorK-Ras-
dc.subject.keywordAuthorRASSF1A-
dc.subject.keywordAuthorROS-
dc.subject.keywordAuthorDNA damage-
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