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

DC Field Value Language
dc.contributor.author김형중-
dc.date.accessioned2014-12-20T16:36:50Z-
dc.date.available2014-12-20T16:36:50Z-
dc.date.issued2011-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/93047-
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.-
dc.description.statementOfResponsibilityopen-
dc.format.extent149~153-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHDNA Damage*-
dc.subject.MESHGenes, ras*-
dc.subject.MESHHumans-
dc.subject.MESHMice-
dc.subject.MESHNIH 3T3 Cells-
dc.subject.MESHReactive Oxygen Species/antagonists & inhibitors-
dc.subject.MESHReactive Oxygen Species/metabolism*-
dc.subject.MESHTumor Suppressor Proteins/genetics-
dc.subject.MESHTumor Suppressor Proteins/metabolism*-
dc.titleRASSF1A suppresses the activated K-Ras-induced oxidative DNA damage.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorSeon Ho Park-
dc.contributor.googleauthorJung Jin Kim-
dc.contributor.googleauthorJin Sil Chung-
dc.contributor.googleauthorSo Ra Lee-
dc.contributor.googleauthorGi Young Lee-
dc.contributor.googleauthorHyung Jung Kim-
dc.contributor.googleauthorYoung Do Yoo-
dc.identifier.doi10.1016/j.bbrc.2011.03.139-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01158-
dc.relation.journalcodeJ00281-
dc.identifier.eissn1090-2104-
dc.identifier.pmid21473856-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0006291X11005626-
dc.subject.keywordK-Ras-
dc.subject.keywordRASSF1A-
dc.subject.keywordROS-
dc.subject.keywordDNA damage-
dc.contributor.alternativeNameKim, Hyung Jung-
dc.contributor.affiliatedAuthorKim, Hyung Jung-
dc.rights.accessRightsnot free-
dc.citation.volume408-
dc.citation.number1-
dc.citation.startPage149-
dc.citation.endPage153-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.408(1) : 149-153, 2011-
dc.identifier.rimsid27994-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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