Proteomic Analysis Reveals a Role for Bcl2-associated Athanogene 3 and Major Vault Protein in Resistance to Apoptosis in Senescent Cells by Regulating ERK1/2 Activation

• DOI: 10.1074/mcp.m114.037697
• Publication Date: 2014-07-06T00:18:38Z
• Authors: Martina P. Pasillas; Sarah Shields; Rebecca Reilly; Jan Strnadel; Christian Behl; Robin Park; John R. Yates; Richard Klemke; Steven L. Gonias; Judith A. Coppinger
• Keywords: Proteomics; 0301 basic medicine; Biochemistry & Molecular Biology; 610; Apoptosis; Breast Neoplasms; Cell Line; 03 medical and health sciences; Antibiotics; Cell Line, Tumor; Breast Cancer; Humans; Cellular Senescence; Cancer; Adaptor Proteins, Signal Transducing; Vault Ribonucleoprotein Particles; Mitogen-Activated Protein Kinase 1; Tumor; Antibiotics, Antineoplastic; Mitogen-Activated Protein Kinase 3; Biomedical and Clinical Sciences; Signal Transducing; Adaptor Proteins; Biological Sciences; Antineoplastic; Doxorubicin; Biochemistry and Cell Biology; Apoptosis Regulatory Proteins; Signal Transduction

Senescence is a prominent solid tumor response to therapy in which cells avoid apoptosis and instead enter into prolonged cell cycle arrest. We applied a quantitative proteomics screen to identify signals that lead to therapy-induced senescence and discovered that Bcl2-associated athanogene 3 (Bag3) is up-regulated after adriamycin treatment in MCF7 cells. Bag3 is a member of the BAG family of co-chaperones that interacts with Hsp70. Bag3 also regulates major cell-signaling pathways. Mass spectrometry analysis of the Bag3 Complex revealed a novel interaction between Bag3 and Major Vault Protein (MVP). Silencing of Bag3 or MVP shifts the cellular response to adriamycin to favor apoptosis. We demonstrate that Bag3 and MVP contribute to apoptosis resistance in therapy-induced senescence by increasing the level of activation of extracellular signal-regulated kinase1/2 (ERK1/2). Silencing of either Bag3 or MVP decreased ERK1/2 activation and promoted apoptosis in adriamycin-treated cells. An increase in nuclear accumulation of MVP is observed during therapy-induced senescence and the shift in MVP subcellular localization is Bag3-dependent. We propose a model in which Bag3 binds to MVP and facilitates MVP accumulation in the nucleus, which sustains ERK1/2 activation. We confirmed that silencing of Bag3 or MVP shifts the response toward apoptosis and regulates ERK1/2 activation in a panel of diverse breast cancer cell lines. This study highlights Bag3-MVP as an important complex that regulates a potent prosurvival signaling pathway and contributes to chemotherapy resistance in breast cancer.