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Mitochondrial VDAC1: function in cell life and death and a target for cancer therapy
1Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel. vardasb@bgu.ac.il
Abstract:
Found at the outer mitochondrial membrane, the voltage-dependent anion channel, VDAC, assumes a crucial position in the cell, serving as the main interface between mitochondrial and cellular metabolisms by mediating transport of ions and metabolites. VDAC thus functions as a gatekeeper, controlling cross-talk between mitochondria and the rest of the cell. Moreover, its location at the boundary between the mitochondria and the cytosol enables VDAC to interact with proteins that mediate and regulate the integration of mitochondrial functions with other cellular activities. Here, we review current knowledge related to the roles played by VDAC in the regulation of cell life and cell death, with relation to cancer. The current concepts of altered metabolism in cancer cells are presented with specific emphasis on mitochondrial, more specifically VDAC1-bound hexokinase (HK), facilitating and promoting the high glycolytic tumor phenotype. In this respect, the up-regulation of HK expression in tumor cells and its binding to VDAC provide both a metabolic benefit and apoptosis-suppressive capacity that offers the cell a growth advantage and increases its resistance to chemotherapy. VDAC has also been recognized as a key protein in mitochondria-mediated apoptosis since it is the proposed target for the pro- and antiapoptotic Bcl-2-family of proteins, as well as due to its function in the release of apoptotic proteins located in the inter-membranal space. These and other functions point to VDAC1 as being a rational target for the development of a new generation of therapeutics.
Insights
Voltage-dependent anion channel (VDAC) regulates cell metabolism and apoptosis. VDAC1, bound to hexokinase, promotes cancer cell growth and chemoresistance, making it a therapeutic target.
Area of Science:
- Mitochondrial biology
- Cancer cell metabolism
- Apoptosis regulation
Background:
- The voltage-dependent anion channel (VDAC) is a crucial protein located on the outer mitochondrial membrane.
- It acts as a gatekeeper, controlling the transport of ions and metabolites between mitochondria and the cytosol.
- VDAC mediates the integration of mitochondrial functions with other cellular activities.
Purpose of the Study:
- To review the roles of VDAC in regulating cell life and death, particularly in the context of cancer.
- To discuss the significance of VDAC1-bound hexokinase (HK) in promoting the Warburg effect in cancer cells.
- To highlight VDAC's involvement in mitochondria-mediated apoptosis and its potential as a therapeutic target.
Main Methods:
- Literature review of current knowledge on VDAC function in cancer.
- Analysis of VDAC's interaction with hexokinase and its impact on cellular metabolism.
- Examination of VDAC's role in apoptosis pathways, including interactions with Bcl-2 family proteins.
Main Results:
- VDAC is central to cellular metabolism and apoptosis.
- VDAC1-bound hexokinase facilitates the high glycolytic phenotype in cancer cells, conferring a growth advantage.
- Increased HK expression and VDAC binding enhance chemoresistance and apoptosis suppression.
- VDAC is a target for Bcl-2 family proteins and mediates the release of apoptotic factors.
Conclusions:
- VDAC plays a multifaceted role in cancer cell survival and proliferation.
- The VDAC1-HK interaction is critical for tumor metabolic reprogramming and resistance to apoptosis.
- VDAC1 represents a promising target for novel cancer therapeutics.
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