# Metformin—A Type 2 Diabetes Mellitus Drug—And Ovarian Cancer: Anticancer Mechanisms and Therapeutic Implications

**Authors:** Emma Sielski, Al-Noumani Shuhd, Ella Bower, Kate Cunningham, Grace Beidel, Alissa Luchianova, Maria Cecilia Courreges, Fabian Benencia

PMC · DOI: 10.3390/biom16030413 · Biomolecules · 2026-03-11

## TL;DR

This paper reviews how metformin, a diabetes drug, may help treat ovarian cancer by affecting cancer cell growth and the tumor environment.

## Contribution

The paper provides a comprehensive review of metformin's anticancer mechanisms and therapeutic potential in ovarian cancer.

## Key findings

- Metformin activates the AMPK pathway to inhibit cancer cell growth and survival.
- Metformin can modulate the tumor microenvironment by affecting macrophages and T cells.
- Preclinical and clinical studies suggest metformin may be a promising therapeutic agent for ovarian cancer.

## Abstract

Ovarian cancer is a devastating disease that is often diagnosed in the late stages. The typical therapeutic approach includes surgery plus cytotoxic drugs such as carboplatin and paclitaxel. In recent years, the advent of poly ADP-ribose polymerase (PARP) inhibitors such as olaparib has offered additional treatment opportunities for patients with BRCA mutations or homologous recombination deficiencies. Nevertheless, resistance to therapy usually occurs, leading to poor overall survival. Therefore, novel treatments are needed for this disease. One of the obstacles to successful treatment is the highly immunosuppressive nature of the ovarian cancer microenvironment. Recent strategies for the treatment of ovarian cancer and other types of cancer involve targeting the metabolism of cancer cells and other cells of the tumor microenvironment. One drug that has been investigated both in preclinical studies and clinical trials as an antitumor agent is metformin. This drug, typically used for the treatment of type-2 diabetes for its capability to lower blood glucose, can directly affect cancer cell growth and survival by activating the AMPK (adenosine monophosphate-activated protein kinase) pathway. Furthermore, it can affect the phenotype of other cells of the tumor microenvironment such as macrophages and T cells. In this review, we summarize the main characteristics of ovarian cancer and describe preclinical studies and clinical trials involving metformin as a therapeutic agent for this disease.

## Linked entities

- **Proteins:** PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1)
- **Chemicals:** metformin (PubChem CID 4091), carboplatin (PubChem CID 426756), paclitaxel (PubChem CID 36314), olaparib (PubChem CID 23725625)
- **Diseases:** type-2 diabetes (MONDO:0005148), ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** PRKAA2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 5563] {aka AMPK, AMPK2, AMPKa2, PRKAA}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}
- **Diseases:** Ovarian Cancer (MESH:D010051), homologous recombination deficiencies (MESH:C535296), cancer (MESH:D009369), Type 2 Diabetes Mellitus (MESH:D003924)
- **Chemicals:** carboplatin (MESH:D016190), Metformin (MESH:D008687), blood glucose (MESH:D001786), olaparib (MESH:C531550), paclitaxel (MESH:D017239)
- **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/PMC13023975/full.md

## References

238 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023975/full.md

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Source: https://tomesphere.com/paper/PMC13023975