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Hydrogen peroxide inhibits non-small cell lung cancer cell anoikis through the inhibition of caveolin-1 degradation
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Metadata
Document Title
Hydrogen peroxide inhibits non-small cell lung cancer cell anoikis through the inhibition of caveolin-1 degradation
Author
Rungtabnapa P, Nimmannit U, Halim H, Rojanasakul Y, Chanvorachote P
Name from Authors Collection
Affiliations
Chulalongkorn University; Chulalongkorn University; National Science & Technology Development Agency - Thailand; National Nanotechnology Center (NANOTEC); West Virginia University
Type
Article
Source Title
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
ISSN
0363-6143
Year
2011
Volume
300
Issue
2
Page
C235-C245
Open Access
Green Published
Publisher
AMER PHYSIOLOGICAL SOC
DOI
10.1152/ajpcell.00249.2010
Format
Abstract
Rungtabnapa P, Nimmannit U, Halim H, Rojanasakul Y, Chanvorachote P. Hydrogen peroxide inhibits non-small cell lung cancer cell anoikis through the inhibition of caveolin-1 degradation. Am J Physiol Cell Physiol 300: C235-C245, 2011. First published December 9, 2010; doi:10.1152/ajpcell.00249.2010.-Anoikis or detachment-induced apoptosis plays an essential role in the regulation of cancer cell metastasis. Caveolin-1 (Cav-1) is a key protein involved in tumor metastasis, but its role in anoikis and its regulation during cell detachment are unclear. We report here that Cav-1 plays a key role as a negative regulator of anoikis through a reactive oxygen species (ROS)-dependent mechanism in human lung carcinoma H460 cells. During cell detachment, Cav-1 is downregulated, whereas ROS generation is upregulated. Hydrogen peroxide and hydroxyl radical are two key ROS produced by cells during detachment. Treatment of the cells with hydrogen peroxide scavengers, catalase and N-acetylcysteine, promoted Cav-1 downregulation and anoikis during cell detachment, indicating that produced hydrogen peroxide plays a primary role in preventing anoikis by stabilizing Cav-1 protein. Catalase and N-acetylcysteine promoted ubiquitination and proteasomal degradation of Cav-1, which is a major pathway of its downregulation during cell anoikis. Furthermore, addition of hydrogen peroxide exogenously to the cells inhibited Cav-1 downregulation by preventing the formation of Cav-1-ubiquitin complex, supporting the inhibitory role of endogenous hydrogen peroxide in Cav-1 degradation during cell detachment. Together, these results indicate a novel role of hydrogen peroxide as an endogenous suppressor of cell anoikis through its stabilizing effect on Cav-1.
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Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Funding Sponsor
National Institutes of Health [R01-HL076340]; Thailand Research Fund [MG5080134]; Chulalongkorn University [F-31-GS-ES13]; NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL076340] Funding Source: NIH RePORTER
License
N/A
Rights
N/A
Publication Source
WOS