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GRIM-19: A Double-edged Sword that Regulates Anti-Tumor and Innate Immune Responses

Authors: Shreeram C. Nallar, Sudhakar Kalakonda, Peng Sun and Dhan V. Kalvakolanu
Publication Date: 17 Mar 2008
Translational Oncogenomics 2008:3 67-79

Shreeram C. Nallar1, Sudhakar Kalakonda1, Peng Sun2 and Dhan V. Kalvakolanu1,2

1Department of Microbiology and Immunology, Marlene and Stewart Greenebaum Cancer Center, 2Molecular and Cellular Cancer Biology, Graduate Program in Life Sciences, University of Maryland School of Medicine, Baltimore, MD 21201.

Abstract

Gene associated with retinoid-interferon-β-induced mortality (GRIM)—19, was originally identifi ed as a critical regulatory protein necessary for Interferon-β-Retinoic acid-induced cell death. Overexpression of GRIM-19 activates cell death and its suppression or inactivation promotes cell growth. GRIM-19 targets multiple proteins/pathways for exerting growth control and cell death. However, GRIM-19 is also required for normal cellular processes. In addition, viruses ‘hijack’ GRIM-19 for their survival. Intracellular bacterial infections and bacterial products have been reported to induce the expression of GRIM-19. In this review, we will discuss the current status of GRIM-19 in growth control and innate immune response.