# Metformin Sensitizes PTEN-deficient Prostate Cancer to PARP Inhibitors by Rebuilding NADP+ Homeostasis

**Authors:** Xiaodong Hao, Zheng Chao, Hao Peng, Xiangdong Guo, Shuo Zheng, Chunyu Zhang, Hao Ding, Yanan Wang, Zirui Xi, Yuan Gao, Guanyu Qu, Yao Zhu, Zhiqiang Chen, Peixiang Lan, Le Li, Zhihua Wang

PMC · DOI: 10.7150/ijbs.121033 · International Journal of Biological Sciences · 2026-01-08

## TL;DR

Metformin can make PTEN-deficient prostate cancer more responsive to PARP inhibitors by restoring NADP+ balance and improving treatment outcomes.

## Contribution

The study reveals a novel metabolic mechanism of PARP inhibitor resistance and proposes metformin as a potential intervention.

## Key findings

- Lactate accumulation activates NHE1/PKC/NOX1 to sustain NADP+ levels, contributing to PARP inhibitor resistance.
- Metformin increases NADP+ levels, enhancing PARP inhibitor efficacy through allosteric effects on PARP structures.
- A machine learning model was developed and validated to predict PARP inhibitor response in PTEN-deficient prostate cancer.

## Abstract

Purpose: DNA repair and DNA damage responses in cancer cells are regulated by metabolic reprogramming, which is increasingly recognized as a key factor contributing to PARP inhibitor (PARPi) treatment failure. This study aims to explore the metabolic mechanisms underlying PARPi resistance in PTEN-deficient prostate cancer and identify clinically viable metabolic interventions to overcome therapy failure.

Experimental Design: A multicenter retrospective cohort was analyzed to evaluate the efficacy of combined metformin-PARPi therapy. Mechanistic studies utilized molecular assays to elucidate PARPi resistance and its critical determinants. Machine learning models predicting PARPi response were developed using clinical datasets and interpreted via SHAP analysis.

Results: In PTEN-deficient cancer cells, lactate accumulation activated the NHE1/PKC/NOX1 axis, sustaining elevated NADP+ levels. NADP+ competitively inhibited the formation of PARPi-PARP-DNA complexes, leading to PARPi resistance. However, metformin administration significantly elevated NADP+ levels, inducing allosteric effects on PARP structures and enhancing PARPi efficacy. Based on these findings, we developed and validated a predictive machine learning model for PARPi response, which was interpreted using SHAP and deployed on a web platform.

Conclusions: Metformin modulates NADP+ levels to influence PARPi sensitivity in PTEN-deficient prostate cancer. Additionally, we developed a machine learning model to provide clinicians with personalized predictions for PARPi response.

## Linked entities

- **Genes:** PTEN (phosphatase and tensin homolog) [NCBI Gene 5728]
- **Proteins:** PARP1 (poly(ADP-ribose) polymerase 1), SLC9A1 (solute carrier family 9 member A1), PRRT2 (proline rich transmembrane protein 2), NOX1 (NADPH oxidase 1)
- **Chemicals:** metformin (PubChem CID 4091), NADP+ (PubChem CID 5885)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, NOX1 (NADPH oxidase 1) [NCBI Gene 27035] {aka GP91-2, MOX1, NOH-1, NOH-1L, NOH1}, SLC9A1 (solute carrier family 9 member A1) [NCBI Gene 6548] {aka APNH, LIKNS, NHE-1, NHE1, PPP1R143}, PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142] {aka ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}
- **Diseases:** cancer (MESH:D009369), Prostate Cancer (MESH:D011471)
- **Chemicals:** Metformin (MESH:D008687), lactate (MESH:D019344), NADP+ (MESH:D009249)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12837654/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12837654/full.md

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Source: https://tomesphere.com/paper/PMC12837654