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.
Abstract:
Resveratrol is a naturally occurring phenolic compound found in various foods such as red wine, chocolate, peanuts, and blueberries. Both in-vitro and in-vivo studies have shown that it has a broad spectrum of pharmacological effects such as providing cellular protection and promoting longevity. These effects include antioxidant, anti-inflammatory, neuroprotective, and anti-viral properties, as well as improvements in cardio-metabolic health and anti-aging benefits. Additionally, resveratrol has demonstrated the ability to induce cell death and inhibit tumor growth across different types and stages of cancer. However, the dual effects of resveratrol-acting to support cell survival in some contexts, while inducing cell death in others-is still not fully understood. In this study, we identify a novel target for resveratrol: the voltage-dependent anion channel 1 (VDAC1), a multi-functional outer mitochondrial membrane protein that plays a key role in regulating both cell survival and death. Our findings show that resveratrol increased VDAC1 expression levels and promoted its oligomerization, leading to apoptotic cell death. Additionally, resveratrol elevated intracellular Ca2+ levels and enhanced the production of reactive oxygen species (ROS). Resveratrol also induced the detachment of hexokinase I from VDAC1, a key enzyme in metabolism, and regulating apoptosis. When VDAC1 expression was silenced using specific siRNA, resveratrol-induced cell death was significantly reduced, indicating that VDAC1 is essential for its pro-apoptotic effects. Additionally, both resveratrol and its analog, trans-2,3,5,4'-tetrahydroxystilbene-2-O-glucoside (TSG), directly interacted with purified VDAC1, as revealed by microscale thermophoresis, with similar binding affinities. However, unlike resveratrol, TSG did not induce VDAC1 overexpression or apoptosis. These results demonstrate that resveratrol-induced apoptosis is linked to increased VDAC1 expression and its oligomerization. This positions resveratrol not only as a protective agent, but also as a pro-apoptotic compound. Consequently, resveratrol offers a promising therapeutic approach for cancer, with potentially fewer side effects compared to conventional treatments, due to its natural origins in plants and food products.
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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