Dysregulation of apoptotic signaling in cancer: molecular mechanisms and therapeutic opportunities

J Plati, O Bucur, R Khosravi‐Far - Journal of cellular …, 2008 - Wiley Online Library
Journal of cellular biochemistry, 2008Wiley Online Library
Apoptosis is a tightly regulated cell suicide program that plays an essential role in the
maintenance of tissue homeostasis by eliminating unnecessary or harmful cells. Defects in
this native defense mechanism promote malignant transformation and frequently confer
chemoresistance to transformed cells. Indeed, the evasion of apoptosis has been
recognized as a hallmark of cancer. Given that multiple mechanisms function at many levels
to orchestrate the regulation of apoptosis, a multitude of opportunities for apoptotic …
Abstract
Apoptosis is a tightly regulated cell suicide program that plays an essential role in the maintenance of tissue homeostasis by eliminating unnecessary or harmful cells. Defects in this native defense mechanism promote malignant transformation and frequently confer chemoresistance to transformed cells. Indeed, the evasion of apoptosis has been recognized as a hallmark of cancer. Given that multiple mechanisms function at many levels to orchestrate the regulation of apoptosis, a multitude of opportunities for apoptotic dysregulation are present within the intricate signaling network of cell. Several of the molecular mechanisms by which cancer cells are protected from apoptosis have been elucidated. These advances have facilitated the development of novel apoptosis‐inducing agents that have demonstrated single‐agent activity against various types of cancers cells and/or sensitized resistant cancer cells to conventional cytotoxic therapies. Herein, we will highlight several of the central modes of apoptotic dysregulation found in cancer. We will also discuss several therapeutic strategies that aim to reestablish the apoptotic response, and thereby eradicate cancer cells, including those that demonstrate resistance to traditional therapies. J. Cell. Biochem. 104: 1124–1149, 2008. © 2008 Wiley‐Liss, Inc.
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