# Synergistic Effects of 2-Deoxyglucose and Diclofenac Sodium on Breast Cancer Cells: A Comparative Evaluation of MDA-231 and MCF7 Cells

**Authors:** Geofrey Ouma Maloba, Tom Were, Erick Barasa, Nasreldeen Mohamed, Arshi Arshi, Ferenc Gallyas

PMC · DOI: 10.3390/ijms26104894 · International Journal of Molecular Sciences · 2025-05-20

## TL;DR

This study shows that combining 2-deoxyglucose and diclofenac sodium can effectively fight breast cancer cells by boosting cell death and reducing their growth.

## Contribution

The study reveals a novel synergistic effect of combining 2-deoxyglucose and diclofenac sodium in breast cancer treatment.

## Key findings

- Combination treatment limits proliferation and enhances cell death in breast cancer cells.
- The drug combination inhibits cell migration and colony formation.
- Cytotoxic effects are similar in MDA-231 and MCF7 cell lines.

## Abstract

Resistance of breast cancers to chemotherapy remains a global challenge to date. Drug combination studies between anti-cancer agents are increasingly becoming therapeutic strategies, geared towards alleviating breast cancers. Previously, 2-deoxyglucose has been shown to target and interrupt glycolysis. Available evidence also suggests that diclofenac, which was originally designed as a pain reliever, could inhibit the proliferation of breast cancer cells. However, the reverse Warburg effect and other metabolic reprogramming mechanisms in breast cancers limit the pharmacological application of both 2-deoxyglucose and diclofenac as mono-therapeutic agents. The present study explores the additive anti-cancer effects of 2-deoxyglucose and diclofenac sodium on breast cancer cells. In this study, MDA-231 and MCF7 cells were treated with 2-deoxyglucose and diclofenac sodium in single and combination doses before being evaluated for viability, cell growth, reactive oxygen species, apoptotic and necrotic phases, and migration abilities. Additionally, immunoblotting of pro-apoptotic proteins, Caspase-3 and Caspase-9, and a hypoxia-inducible factor-1 alpha, was also performed. The results showed that combination treatments of the cells with the drugs exhibited additive anti-cancer effects by limiting proliferation, enhancing cytotoxic reactive oxygen species generation, enhancing apoptosis and necrosis, limiting colony formation and expansion of cells, and inhibiting cell migration. The degrees of cytotoxicity of combined treatments were almost similar in both cell lines, although with minimal differences. Put together, these results reveal the novel synergistic effects of 2-deoxyglucose and diclofenac sodium on breast cancer cells, hence potentially elevating their pharmacological profile in the overall breast cancer therapy.

## Linked entities

- **Proteins:** Casp3 (caspase 3), Casp9 (caspase 9)
- **Chemicals:** 2-deoxyglucose (PubChem CID 108223), diclofenac sodium (PubChem CID 5018304)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, CASP9 (caspase 9) [NCBI Gene 842] {aka APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56}
- **Diseases:** cytotoxic (MESH:D064420), cancer (MESH:D009369), pain (MESH:D010146), necrosis (MESH:D009336), Breast Cancer (MESH:D001943)
- **Chemicals:** Diclofenac Sodium (MESH:D004008), 2-Deoxyglucose (MESH:D003847), reactive oxygen species (MESH:D017382)
- **Cell lines:** MCF7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031), MDA-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12112485/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12112485/full.md

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Source: https://tomesphere.com/paper/PMC12112485