Implication of 14‐3‐3ε and 14‐3‐3θ/τ in proteasome inhibition‐induced apoptosis of glioma cells. Issue 1 (28th November 2012)

• Record Type: Journal Article
• Authors: Yan, Ying; Xu, Ying; Gao, Yan‐Yan; Zong, Zhi‐Hong; Zhang, Qiang; Li, Chao; Wang, Hua‐Qin
• Is Part Of: Cancer science. Volume 104:Issue 1(2013:Jan.)
• Page Start: 55
• Page End: 61
• Publication Date: 2012-11-28
• Subjects: Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.12033
• Languages: English
• ISSNs: 1347-9032

Abstract

<abstract abstract-type="main" id="cas12033-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Proteasome inhibitors represent a novel class of anticancer agents that are used in the treatment of hematologic malignancies and various solid tumors. However, mechanisms underlying their anticancer actions were not fully understood. It has been reported that strong 14‐3‐3 protein expression is observed and associated with tumor genesis and progression of astrocytoma. In addition, global inhibition of 14‐3‐3 functions with a general 14‐3‐3 antagonist difopein induces apoptosis of human astrocytoma cells, validating 14‐3‐3 as a potential molecular target for anticancer therapeutic management. In the current study, for the first time we demonstrated that proteasome inhibitors downregulated 14‐3‐3ε and 14‐3‐3θ/τ in U87 and SF295 glioma cells. Overexpression of 14‐3‐3ε and 14‐3‐3θ/τ significantly suppressed apoptosis of human glioma cells induced by proteasome inhibitors. We also demonstrated that MG132 activated ASK1 and siASK1 compromised the MG132‐induced apoptosis of glioma cells. Furthermore, overexpression of 14‐3‐3ε and 14‐3‐3θ/τ markedly suppressed activation of ASK1. Collectively, the current study supported that proteasome inhibitors, at least in part, caused cytotoxicity of glioma cells via downregulation of 14‐3‐3ε and 14‐3‐3θ/τ and subsequent activation of ASK1. (<italic>Cancer Sci</italic> 2013; 104: 55–61)</p> </abstract>