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

Authors
 Seon Ho Park  ;  Jung Jin Kim  ;  Jin Sil Chung  ;  So Ra Lee  ;  Gi Young Lee  ;  Hyung Jung Kim  ;  Young Do Yoo 
Citation
 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol.408(1) : 149-153, 2011 
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN
 0006-291X 
Issue Date
2011
MeSH
Animals ; Cell Line, Tumor ; DNA Damage* ; Genes, ras* ; Humans ; Mice ; NIH 3T3 Cells ; Reactive Oxygen Species/antagonists & inhibitors ; Reactive Oxygen Species/metabolism* ; Tumor Suppressor Proteins/genetics ; Tumor Suppressor Proteins/metabolism*
Keywords
K-Ras ; RASSF1A ; ROS ; DNA damage
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.
Full Text
http://www.sciencedirect.com/science/article/pii/S0006291X11005626
DOI
10.1016/j.bbrc.2011.03.139
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Hyung Jung(김형중) ORCID logo https://orcid.org/0000-0003-2498-0683
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/93047
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