Heat Shock Protein 70 (Hsp70) Suppresses RIP1-Dependent Apoptotic and Necroptotic Cascades

• Published in: Molecular cancer research Vol. 16; no. 1; pp. 58 - 68
• Main Authors: Srinivasan, Sharan R, Cesa, Laura C, Li, Xiaokai, Julien, Olivier, Zhuang, Min, Shao, Hao, Chung, Jooho, Maillard, Ivan, Wells, James A, Duckett, Colin S, Gestwicki, Jason E
• Format: Journal Article
• Language: English
• Published: United States American Association for Cancer Research Inc 01.01.2018
• Subjects: Apoptosis; Apoptosis - physiology; Biomarkers; Breast cancer; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cancer; Cascades; Cell death; Cell Line, Tumor; Clients; Female; Heat shock proteins; HSP70 Heat-Shock Proteins - antagonists & inhibitors; HSP70 Heat-Shock Proteins - genetics; HSP70 Heat-Shock Proteins - metabolism; Hsp70 protein; Hsp90 protein; Humans; Inhibition; Inhibitors; Jurkat Cells; MCF-7 Cells; Necroptosis; Necrosis; Receptor-Interacting Protein Serine-Threonine Kinases - genetics; Receptor-Interacting Protein Serine-Threonine Kinases - metabolism; Regulators; Signal Transduction; Signaling; XIAP protein
• ISSN: 1541-7786; 1557-3125
• DOI: 10.1158/1541-7786.MCR-17-0408

Hsp70 is a molecular chaperone that binds to "client" proteins and protects them from protein degradation. Hsp70 is essential for the survival of many cancer cells, but it is not yet clear which of its clients are involved. Using structurally distinct chemical inhibitors, we found that many of the well-known clients of the related chaperone, Hsp90, are not strikingly responsive to Hsp70 inhibition. Rather, Hsp70 appeared to be important for the stability of the RIP1 (RIPK1) regulators: cIAP1/2 (BIRC1 and BIRC3), XIAP, and cFLIP (CFLAR). These results suggest that Hsp70 limits apoptosis and necroptosis pathways downstream of RIP1. Consistent with this model, MDA-MB-231 breast cancer cells treated with Hsp70 inhibitors underwent apoptosis, while cotreatment with z-VAD.fmk switched the cell death pathway to necroptosis. In addition, cell death in response to Hsp70 inhibitors was strongly suppressed by RIP1 knockdown or inhibitors. Thus, these data indicate that Hsp70 plays a previously unrecognized and important role in suppressing RIP1 activity. These findings clarify the role of Hsp70 in prosurvival signaling and suggest IAPs as potential new biomarkers for Hsp70 inhibition. .