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Anticancer Molecular Mechanisms of Resveratrol

Open access
Varoni, Elena M., Lo Faro, Alfredo Fabrizio, Sharifi-Rad, Javad, Iriti, Marcello·2016·Frontiers in Nutrition

Abstract

Resveratrol is a pleiotropic phytochemical belonging to the stilbene family. Though it is only significantly present in grape products, a huge amount of preclinical studies investigated its anticancer properties in a plethora of cellular and animal models. Molecular mechanisms of resveratrol involved signaling pathways related to extracellular growth factors and receptor tyrosine kinases; formation of multiprotein complexes and cell metabolism; cell proliferation and genome instability; cytoplasmic tyrosine kinase signaling (cytokine, integrin, and developmental pathways); signal transduction by the transforming growth factor-β super-family; apoptosis and inflammation; and immune surveillance and hormone signaling. Resveratrol also showed a promising role to counteract multidrug resistance: in adjuvant therapy, associated with 5-fluoruracyl and cisplatin, resveratrol had additive and/or synergistic effects increasing the chemosensitization of cancer cells. Resveratrol, by acting on diverse mechanisms simultaneously, has been emphasized as a promising, multi-target, anticancer agent, relevant in both cancer prevention and treatment.

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Metadata

Authors
Varoni, E. M., Lo Faro, A. F., Sharifi-Rad, J., & Iriti, M.
Venue
Frontiers in Nutrition
Published
2016-04-12
Volume
3
Pages
8-8
ISSN
2296-861X (ISSN-L)
OpenAlex
W2337558949
Cited by
401
References
0
FWCI
23.87
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Anticancer Molecular Mechanisms of Resveratrol. https://app.cochat.ai/papers/10.3389/fnut.2016.00008
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Varoni, E. M., Lo Faro, A. F., Sharifi-Rad, J., & Iriti, M. (2016). Anticancer Molecular Mechanisms of Resveratrol. Frontiers in Nutrition. https://doi.org/10.3389/fnut.2016.00008

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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