4.7 Review

Apoptotic proteins with non-apoptotic activity: expression and function in cancer

Journal

APOPTOSIS
Volume 28, Issue 5-6, Pages 730-753

Publisher

SPRINGER
DOI: 10.1007/s10495-023-01835-3

Keywords

Apoptosis; Cancer; Metabolism; Mitochondria; SMAC; Diablo; VDAC1

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Apoptosis is a regulated cell death process that maintains tissue integrity. It involves two major pathways: the extrinsic pathway, activated by external signals, and the intrinsic pathway, activated by DNA damage or stress. However, apoptotic proteins also have non-death-related functions, particularly in non-cancer cells. This review highlights the unconventional roles of apoptotic proteins, focusing on VDAC1 and SMAC/Diablo, mitochondrial proteins that are overexpressed in cancer cells.
Apoptosis is a process of programmed cell death in which a cell commits suicide while maintaining the integrity and architecture of the tissue as a whole. Apoptosis involves activation of one of two major pathways: the extrinsic pathway, where extracellular pro-apoptotic signals, transduced through plasma membrane death receptors, activate a caspase cascade leading to apoptosis. The second, the intrinsic apoptotic pathway, where damaged DNA, oxidative stress, or chemicals, induce the release of pro-apoptotic proteins from the mitochondria, leading to the activation of caspase-dependent and independent apoptosis. However, it has recently become apparent that proteins involved in apoptosis also exhibit non-cell death-related physiological functions that are related to the cell cycle, differentiation, metabolism, inflammation or immunity. Such non-conventional activities were predominantly reported in non-cancer cells although, recently, such a dual function for pro-apoptotic proteins has also been reported in cancers where they are overexpressed. Interestingly, some apoptotic proteins translocate to the nucleus in order to perform a non-apoptotic function. In this review, we summarize the unconventional roles of the apoptotic proteins from a functional perspective, while focusing on two mitochondrial proteins: VDAC1 and SMAC/Diablo. Despite having pro-apoptotic functions, these proteins are overexpressed in cancers and this apparent paradox and the associated pathophysiological implications will be discussed. We will also present possible mechanisms underlying the switch from apoptotic to non-apoptotic activities although a deeper investigation into the process awaits further study.

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