Resveratrol's Pro-Apoptotic Effects in Cancer Are Mediated Through the Interaction and Oligomerization of the

Tal Raviv1, Anna Shteinfer-Kuzmine2, Meital M Moyal2

  • 1Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.

Insights

Resveratrol induces cancer cell death by increasing the expression and oligomerization of voltage-dependent anion channel 1 (VDAC1). This natural compound shows promise as a targeted cancer therapy.

Area of Science:

  • Mitochondrial Biology
  • Molecular Pharmacology
  • Cancer Therapeutics

Background:

  • Resveratrol, a natural phenolic compound, exhibits diverse pharmacological effects including antioxidant, anti-inflammatory, and anti-cancer properties.
  • The dual role of resveratrol in promoting cell survival and inducing cell death remains incompletely understood.
  • Voltage-dependent anion channel 1 (VDAC1) is a key mitochondrial protein involved in regulating cell survival and apoptosis.

Purpose of the Study:

  • To identify novel molecular targets of resveratrol.
  • To elucidate the mechanism by which resveratrol induces cancer cell death.
  • To investigate the role of VDAC1 in resveratrol's pro-apoptotic effects.

Main Methods:

  • Assessed resveratrol's effects on VDAC1 expression, oligomerization, and interaction with hexokinase I.
  • Measured intracellular calcium (Ca2+) levels and reactive oxygen species (ROS) production.
  • Utilized VDAC1-specific siRNA to evaluate the necessity of VDAC1 in resveratrol-induced apoptosis.
  • Employed microscale thermophoresis to analyze the direct interaction between resveratrol, its analog TSG, and purified VDAC1.

Main Results:

  • Resveratrol increased VDAC1 expression and promoted its oligomerization, leading to apoptotic cell death.
  • Resveratrol elevated intracellular Ca2+ and ROS levels, and induced hexokinase I detachment from VDAC1.
  • Silencing VDAC1 expression significantly reduced resveratrol-induced cell death, confirming VDAC1's essential role.
  • Resveratrol and its analog TSG bound to VDAC1, but only resveratrol induced VDAC1 overexpression and apoptosis.

Conclusions:

  • Resveratrol-induced apoptosis is critically dependent on increased VDAC1 expression and subsequent oligomerization.
  • Resveratrol acts as a pro-apoptotic agent through VDAC1 modulation, in addition to its protective roles.
  • Resveratrol represents a promising, naturally derived therapeutic agent for cancer treatment with potential for reduced side effects.

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