# Resveratrol Mimics Exercise-Induced Metabolic Stress to Suppress CIP2A and Epithelial–Mesenchymal Transition in 3D Renal Carcinoma Spheroids

**Authors:** Bang Sub Lee, Jong-Shik Kim, Wi-Young So

PMC · DOI: 10.3390/biomedicines14030599 · Biomedicines · 2026-03-08

## TL;DR

This study shows that resveratrol, when applied over six days, reduces cancer-related proteins in 3D kidney cancer models, mimicking the effects of metabolic stress.

## Contribution

The study introduces a novel 6-day resveratrol treatment regimen in 3D renal carcinoma spheroids to suppress CIP2A and mesenchymal markers.

## Key findings

- Resveratrol reduced 2D cell viability and induced stress-associated morphological changes.
- Resveratrol decreased CIP2A protein levels and mesenchymal markers in 3D spheroids.
- The treatment mimicked metabolic stress responses in kidney cancer cells.

## Abstract

Background/Objectives: We evaluated a 6-day repeated resveratrol exposure regimen in a three-dimensional (3D) culture model of human renal cell carcinoma (Caki-1) spheroids to examine phenotypic responses and changes in CIP2A abundance and epithelial–mesenchymal transition (EMT)-associated marker expression. Methods: Over 6 days, we assessed morphology and 2D cell viability and quantified CIP2A, fibronectin, and α-SMA by immunoblotting and immunofluorescence. Results: Resveratrol reduced 2D viability and increased cytoplasmic vacuoles, consistent with a stress-associated morphological response. In 3D spheroids, resveratrol treatment was associated with reduced CIP2A protein levels and decreased fibronectin and α-SMA, consistent with attenuation of a mesenchymal marker profile. Conclusions: These proof-of-concept data link 6-day resveratrol exposure to CIP2A reduction and decreased mesenchymal marker expression in a human 3D RCC spheroid system; however, PP2A activity and downstream signaling, AMPK/SIRT1 activation, and EMT-relevant functional assays were not assessed, and validation across additional RCC models will be required.

## Linked entities

- **Genes:** CIP2A (cellular inhibitor of PP2A) [NCBI Gene 57650], fn1.S (fibronectin 1 S homeolog) [NCBI Gene 397744], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58]
- **Proteins:** CIP2A (cellular inhibitor of PP2A), fn1.S (fibronectin 1 S homeolog), ACTA1 (actin alpha 1, skeletal muscle), PTPA (protein phosphatase 2 phosphatase activator)
- **Chemicals:** resveratrol (PubChem CID 5056)
- **Diseases:** renal cell carcinoma (MONDO:0005086)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CIP2A (cellular inhibitor of PP2A) [NCBI Gene 57650] {aka KIAA1524, NOCIVA, p90}, PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562] {aka AMPK, AMPK alpha 1, AMPKa1}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, PTPA (protein phosphatase 2 phosphatase activator) [NCBI Gene 5524] {aka PARK25, PP2A, PPP2R4, PR53}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}
- **Diseases:** RCC (MESH:D002292)
- **Chemicals:** Resveratrol (MESH:D000077185)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024014/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024014/full.md

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Source: https://tomesphere.com/paper/PMC13024014