Cited 7 times in
RASSF1A suppresses the activated K-Ras-induced oxidative DNA damage.
DC Field | Value | Language |
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dc.contributor.author | 김형중 | - |
dc.date.accessioned | 2014-12-20T16:36:50Z | - |
dc.date.available | 2014-12-20T16:36:50Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/93047 | - |
dc.description.abstract | The 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.statementOfResponsibility | open | - |
dc.format.extent | 149~153 | - |
dc.relation.isPartOf | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Cell Line, Tumor | - |
dc.subject.MESH | DNA Damage* | - |
dc.subject.MESH | Genes, ras* | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | NIH 3T3 Cells | - |
dc.subject.MESH | Reactive Oxygen Species/antagonists & inhibitors | - |
dc.subject.MESH | Reactive Oxygen Species/metabolism* | - |
dc.subject.MESH | Tumor Suppressor Proteins/genetics | - |
dc.subject.MESH | Tumor Suppressor Proteins/metabolism* | - |
dc.title | RASSF1A suppresses the activated K-Ras-induced oxidative DNA damage. | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학) | - |
dc.contributor.googleauthor | Seon Ho Park | - |
dc.contributor.googleauthor | Jung Jin Kim | - |
dc.contributor.googleauthor | Jin Sil Chung | - |
dc.contributor.googleauthor | So Ra Lee | - |
dc.contributor.googleauthor | Gi Young Lee | - |
dc.contributor.googleauthor | Hyung Jung Kim | - |
dc.contributor.googleauthor | Young Do Yoo | - |
dc.identifier.doi | 10.1016/j.bbrc.2011.03.139 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A01158 | - |
dc.relation.journalcode | J00281 | - |
dc.identifier.eissn | 1090-2104 | - |
dc.identifier.pmid | 21473856 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0006291X11005626 | - |
dc.subject.keyword | K-Ras | - |
dc.subject.keyword | RASSF1A | - |
dc.subject.keyword | ROS | - |
dc.subject.keyword | DNA damage | - |
dc.contributor.alternativeName | Kim, Hyung Jung | - |
dc.contributor.affiliatedAuthor | Kim, Hyung Jung | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 408 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 149 | - |
dc.citation.endPage | 153 | - |
dc.identifier.bibliographicCitation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.408(1) : 149-153, 2011 | - |
dc.identifier.rimsid | 27994 | - |
dc.type.rims | ART | - |
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