Anti-Cancer Compounds Targeted to VDAC: Potential and Perspectives

Author(s): Simona Reina*, Vito De Pinto *.

Journal Name: Current Medicinal Chemistry

Volume 24 , Issue 40 , 2017

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Abstract:

Background: VDAC (Voltage-Dependent Anion selective Channel) is a small family of abundant pore-forming proteins located in the outer mitochondrial membrane. Their role range from the most intuitive, the formation of a hydrophilic conduit through the membrane thanks to its beta-barrel structure, to less understood functions that make them essential actors in the cross-talk between the bioenergetics metabolism and the cytosol components. Due to this localization, VDAC1, in particular, has been reported to be involved in apoptosis, Hexokinase and tubulin binding, and in the Warburg effect. For these reasons, an involvement of VDAC in cancer is considered consequential and a number of compounds have been proposed and used in experimental trials to demonstrate the efficacy of molecules affecting the functions of VDAC.

Objectives: In this work, we thus survey the literature describing drug compounds acting on the cancerous proliferation through VDAC. Three main categories have been assigned: molecules acting on the VDAC-Hexokinase binding, molecules directly inhibiting the VDAC conductance, molecules affecting the expression levels of the VDAC gene. The application of biological peptides for this purpose is also considered.

Conclusion: Since the knowledges about the functional properties of VDAC protein are still insufficient, VDAC as a pharmacological target in the fight against cancer is still a very open, but very promising, field.

Keywords: VDAC, Mitochondrial dysfunction, cancer, apoptosis, hexokinase, warburg effect, outer mitochondrial membrane.

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Article Details

VOLUME: 24
ISSUE: 40
Year: 2017
Page: [4447 - 4469]
Pages: 23
DOI: 10.2174/0929867324666170530074039
Price: $58

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