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Int J Cancer ; 128(8): 1989-95, 2011 Apr 15.
Article in English | MEDLINE | ID: mdl-20549705

ABSTRACT

The p14(ARF) is a key tumor suppressor induced mainly by oncogenic stimuli. Although p14(ARF) does not seem to respond to DNA damage, there are very few data regarding its role in other forms of stress, such as heat shock (HS) and oxidative stress (OS). Here, we report that suppression of p14(ARF) increased resistance to cell death when cells were treated with H(2) O(2) or subjected to HS. In this setting, protection from cell death was mediated by elevated levels and activity of ß-catenin, as downregulation of ß-catenin alleviated the protective role of p14(ARF) silencing. Moreover, Hsp70 was shown to regulate ß-catenin protein levels by interacting with p14(ARF) , suggesting that Hsp70, p14(ARF) and ß-catenin form a regulatory network. This novel pathway triggers cell death signals when cells are exposed to HS and OS.


Subject(s)
Apoptosis , HSP72 Heat-Shock Proteins/metabolism , Heat-Shock Response , Oxidative Stress , Tumor Suppressor Protein p14ARF/metabolism , beta Catenin/metabolism , Blotting, Western , Cell Proliferation , Flow Cytometry , Gene Expression Regulation, Neoplastic , HSP72 Heat-Shock Proteins/genetics , Humans , Immunoprecipitation , Luciferases/metabolism , Neoplasms/genetics , Neoplasms/metabolism , Neoplasms/pathology , RNA, Messenger/genetics , RNA, Small Interfering/genetics , Reverse Transcriptase Polymerase Chain Reaction , Tumor Cells, Cultured , Tumor Suppressor Protein p14ARF/antagonists & inhibitors , Tumor Suppressor Protein p14ARF/genetics , Up-Regulation , beta Catenin/genetics
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