# Therapeutic Potential of Resveratrol in Cancer and Neurodegenerative Disorders: A Current Review

**Authors:** Kenly Wuputra, Chia‐Che Ku, Ying‐Chu Lin, Yi‐Chun Tsai, Deng‐Chyang Wu, Yukio Mitsui, Maki Satou, Yuuki Tanaka, Shigeo Saito, Kazunari K. Yokoyama

PMC · DOI: 10.1002/biof.70080 · 2026-01-26

## TL;DR

Resveratrol shows promise in treating cancer and neurodegenerative diseases by targeting multiple biological pathways, but its effectiveness is limited by poor solubility and bioavailability.

## Contribution

This review highlights resveratrol's multi-target therapeutic potential and the need for improved delivery methods to enhance its clinical application.

## Key findings

- Resveratrol modulates pathways like TP53, NRF2, and NF-κB to induce cancer cell death.
- Poor bioavailability and stability of resveratrol require advanced delivery strategies like nanoencapsulation.
- Resveratrol's antioxidant effects involve ROS regulation and activation of SIRT1 and AMPK signaling.

## Abstract

Resveratrol (RSV; 3,5,4′‐trihydroxy‐trans‐stilbene) is a natural polyphenolic compound with notable antioxidant, anti‐inflammatory, and immunomodulatory properties. It has been investigated for therapeutic applications in cardiovascular disease, cancer, and neurodegenerative disorders. This review emphasizes the potential of RSV in oncology and neuroprotection, synthesizing evidence from systematic database searches and experimental studies. Despite promising biological activities, RSV is limited by poor stability, low aqueous solubility, rapid metabolism, and restricted bioavailability, necessitating improved delivery strategies such as nanoencapsulation, nanocrystals, prodrugs, and structural analogues. Mechanistically, RSV exerts anticancer and neuroprotective effects through modulation of p53, STAT3, NF‐κB, and mitochondrial‐mediated apoptosis. Its antioxidant actions involve regulation of reactive oxygen species (ROS), activation of NRF2, AMPK signaling, and SIRT1. RSV and related antioxidants act on multiple molecular pathways, including TP53, β‐catenin, STAT3, NF‐κB, NRF2–AMPK, PI3K/AKT, and SIRT1, to regulate inflammation and cell death. The balance between oxidative and antioxidative processes is critical for therapeutic efficacy. Notably, RSV‐induced ROS‐mediated cell death, particularly in the context of TP53 mutations, represents a promising target for future interventions. Overall, RSV demonstrates multi‐target potential for cancer and neurodegenerative disease therapy, though optimization of its pharmacological profile remains essential.

Resveratrol induces the expressions of TP53, NRF2, and JDP2 axis in cancer cells to control ROS balance in mitochondria. The antioxidation responses were induced through SRIT1/3, HDAC, STAT3, TGFβ, and so on, to trigger the inflammation, and NFkB response to lead to the cell death of cancers or neuro‐damaged cells.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], SIRT1 (sirtuin 1) [NCBI Gene 23411], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], JDP2 (Jun dimerization protein 2) [NCBI Gene 122953], HDAC9 (histone deacetylase 9) [NCBI Gene 9734], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040]
- **Chemicals:** Resveratrol (PubChem CID 5056)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}
- **Diseases:** Cancer (MESH:D009369), Neurodegenerative Disorders (MESH:D019636), inflammation (MESH:D007249), cardiovascular disease (MESH:D002318)
- **Chemicals:** 3,5,4'-trihydroxy-trans-stilbene (-), RSV (MESH:D000077185), ROS (MESH:D017382)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12835470/full.md

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Source: https://tomesphere.com/paper/PMC12835470