# Citrus limon Peel Extract Modulates Redox Enzymes and Induces Cytotoxicity in Human Gastric Cancer Cells

**Authors:** Rosarita Nasso, Rosario Rullo, Antonio D’Errico, Pierluigi Reveglia, Lucia Lecce, Annarita Poli, Paola Di Donato, Gaetano Corso, Emmanuele De Vendittis, Rosaria Arcone, Mariorosario Masullo

PMC · DOI: 10.3390/ijms27020598 · 2026-01-07

## TL;DR

Lemon peel extract shows potential as a natural treatment for gastric cancer by reducing cell viability and disrupting antioxidant enzymes.

## Contribution

The study demonstrates that Citrus limon peel extract induces cytotoxicity and modulates redox enzymes in gastric cancer cells.

## Key findings

- LPE significantly reduced cell viability and clonogenic potential in gastric cancer cells.
- LPE modulated redox homeostasis by altering ROS levels and decreasing SOD and CAT protein expression.
- LPE inhibited CAT activity in a dose-dependent manner with an IC50 of 0.008 mg/mL.

## Abstract

Gastric cancer remains a leading cause of cancer-related mortality worldwide. Citrus fruits are rich in polyphenols, exerting antioxidant and chemo-preventive activities, and lemon peel represents a valuable source of such bioactive compounds. Previous studies showed that Citrus limon peel extracts (LPE) inhibited the activity of some enzymes of the antioxidant system and reduced the interleukin-6-dependent invasiveness of gastric and colon cancer cells. In the present study, we have investigated the effects of LPE on the human gastric adenocarcinoma AGS and MKN-28 cells and on the activity of a crucial redox enzyme, catalase (CAT). Indeed, LPE significantly reduced the cell viability and clonogenic potential of the gastric cancer cells and induced morphological changes indicative of cytotoxicity. Moreover, LPE modulated the intracellular redox homeostasis by decreasing levels of the hydrogen peroxide-related reactive oxygen species (ROS) while increasing those of superoxide anions and decreasing levels of superoxide dismutases (SODs). Western blotting analysis revealed that LPE downregulated CAT, SOD-1, SOD-2, and monoamine oxidase A (MAO-A) protein expression level in both cell lines. Finally, the extract inhibited CAT activity in a dose-dependent manner (IC50 = 0.008 ± 0.003 mg/mL; Ki = 0.012 ± 0.002 mg/mL). These findings indicate that LPE exerts cytotoxic and redox-modulating effects through the inhibition of antioxidant enzymes and the alteration of ROS balance. Therefore, the agro-industrial by-product LPE could be considered as a promising natural source of polyphenolic compounds with potential applications in the prevention and therapy of gastric cancer.

## Linked entities

- **Proteins:** CAT (catalase), SOD1 (superoxide dismutase 1), SOD2 (superoxide dismutase 2), MAOA (monoamine oxidase A)
- **Chemicals:** hydrogen peroxide (PubChem CID 784)
- **Diseases:** gastric cancer (MONDO:0001056)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** SOD2 (superoxide dismutase 2) [NCBI Gene 6648] {aka GC1, GClnc1, IPO-B, IPOB, MNSOD, MVCD6}, CAT (catalase) [NCBI Gene 847], SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, MAOA (monoamine oxidase A) [NCBI Gene 4128] {aka BRNRS, MAO-A}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** Cytotoxicity (MESH:D064420), Gastric Cancer (MESH:D013274), cancer (MESH:D009369)
- **Chemicals:** hydrogen peroxide (MESH:D006861), ROS (MESH:D017382), polyphenols (MESH:D059808), Citrus limon Peel (-), superoxide anions (MESH:D013481)
- **Species:** Homo sapiens (human, species) [taxon 9606], Citrus x limon (lemon, species) [taxon 2708]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12841246/full.md

---
Source: https://tomesphere.com/paper/PMC12841246