Bcl-2 regulation of the inositol 1,4,5-trisphosphate receptor and calcium signaling in normal and malignant lymphocytes: Potential new target for cancer treatment |
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Authors: | Edward F. Greenberg Andrew R. Lavik Clark W. Distelhorst |
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Affiliation: | 1. Division of Hematology/Oncology, Case Western Reserve University School of Medicine, Case Comprehensive Cancer Center, University Hospitals Case Medical Center, USA;2. MetroHealth Medical Center, USA |
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Abstract: | The anti-apoptotic protein Bcl-2 is a versatile regulator of cell survival. Its interactions with its own pro-apoptotic family members are widely recognized for their role in promoting the survival of cancer cells. These interactions are thus being targeted for cancer treatment. Less widely recognized is the interaction of Bcl-2 with the inositol 1,4,5-trisphosphate receptor (InsP3R), an InsP3-gated Ca2 + channel located on the endoplasmic reticulum. The nature of this interaction, the mechanism by which it controls Ca2 + release from the ER, its role in T-cell development and survival, and the possibility of targeting it as a novel cancer treatment strategy are summarized in this review. This article is part of a Special Issue entitled: Calcium signaling in health and disease. Guest Editors: Geert Bultynck, Jacques Haiech, Claus W. Heizmann, Joachim Krebs, and Marc Moreau. |
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Keywords: | Bcl-2, B-cell leukemia/lymphoma-2 BH, Bcl-2 homology CaN, calcineurin ER, endoplasmic reticulum IDP, inositol 1,4,5-trisphosphate receptor-derived peptide InsP3, inositol 1,4,5-trisphosphate InsP3R, inositol 1,4,5-trisphosphate receptor SERCA, Sarcoplasmic/Endoplasmic Reticulum-associated Ca2 +-ATPase TCR, T-cell receptor |
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