Regulation of XIAP Translation and Induction by MDM2 following Irradiation

• Type of Material: Article
• Authors: Lubing Gu, Emory University; Ningxi Zhu, Emory University; Hongying Zhang, Emory University; Donald L. Durden, Emory University; Yue Feng, Emory University; Muxiang Zhou, Emory University
• Language: English
• Date: 2009-05-05
• Publisher: Elsevier (Cell Press): 12 month embargo
• Publication Version: Author Accepted Manuscript (After Peer Review)
• Copyright Statement: © 2009 Elsevier Inc.
• License: Creative Commons Attribution-NonCommerical-NoDerivs 3.0 Unported
• Final Published Version (URL): http://dx.doi.org/10.1016/j.ccr.2009.03.002
• Title of Journal or Parent Work: Cancer Cell
• ISSN: 1535-6108
• Volume: 15
• Issue: 5
• Start Page: 363
• End Page: 375
• Grant/Funding Information: This work was supported by grants from NIH (R01 CA123490), The Leukemia and Lymphoma Society (6033-08), and CURE.
• Research Categories: Health Sciences, Oncology; Biology, Cell; Health Sciences, Pharmacology

Abstract

Increases in protein levels of XIAP in cancer cells have been associated with resistance to apoptosis induced by cellular stress. Herein we demonstrate that the upregulation of XIAP protein levels is regulated by MDM2 at the translational level. MDM2 was found to physically interact with the IRES of the XIAP 5′-UTR, and to positively regulate XIAP IRES activity. This XIAP IRES-dependent translation was significantly increased in MDM2-transfected cells where MDM2 accumulated in the cytoplasm. Cellular stress and DNA damage triggered by irradiation induced the dephosphorylation and cytoplasmic localization of MDM2, which also led to an increase in IRES-dependent XIAP translation. Upregulation of XIAP in MDM2-overexpressing cancer cells in response to irradiation resulted in resistance of these cells to radiation-induced apoptosis.Significance Overexpression of the MDM2 oncoprotein, which is often found in cancer cells, is associated with resistance to chemo-radiation therapy and poor prognosis of cancer patients. MDM2 is well characterized as an inhibitor of the tumor suppressor p53, and overexpression of MDM2 contributes to a growth advantage for cancer cells. However, the mechanism by which overexpression of MDM2 confers resistance to DNA damage induced by irradiation and chemotherapy are not fully elucidated. We report here that MDM2 was able to bind to XIAP mRNA and positively regulate the IRES-dependent XIAP translation during cellular stress triggered by irradiation. These results identify a p53-independent function for MDM2 in mediating XIAP translation, which is critical in effecting cancer cell response to chemo-radiation therapy.