# Investigating the Mechanisms of Combined Therapy for MCF-7 Breast Cancer Cells Using Arsenic Trioxide and Resveratrol through Network Pharmacology

**Authors:** Hongye Hu, Yanzhi Wu, Jingwei Hong, Huiying Wang, Xiaohua Zhang, Guanli Huang, Xiaofang Zhu

PMC · DOI: 10.1007/s43657-025-00218-9 · Phenomics · 2025-12-19

## TL;DR

This study explores how combining arsenic trioxide and resveratrol can more effectively treat breast cancer by reducing key cancer-related proteins.

## Contribution

The study reveals the combined therapeutic mechanism of arsenic trioxide and resveratrol in breast cancer treatment.

## Key findings

- The combination of ATO and resveratrol more effectively inhibits ESR1, TP53, and AKT1 in MCF-7 cells than either agent alone.
- The combination promotes cell apoptosis by suppressing these key proteins.
- ATO and resveratrol together may offer a promising strategy for breast cancer treatment.

## Abstract

Breast cancer (BC) remains the predominant form of cancer among women. Arsenic trioxide (ATO), an element in traditional Chinese medicine, has shown potential for treating BC, particularly when combined with resveratrol. However, the exact mechanisms of their combined action are not fully understood. This study aims to clarify their combined mechanisms through network pharmacology and experimental validation. In vitro experiments confirmed that compared with either agent alone, the combination of ATO and resveratrol more effectively inhibited the production of estrogen receptor 1 (ESR1), tumor protein P53 (TP53), and v-AKT murine thymoma viral oncogene homolog 1 (AKT1) in MCF-7 cells. Our findings indicate that the combination of ATO and resveratrol significantly promotes cell apoptosis by suppressing ESR1, TP53, and AKT1. Thus, ATO and resveratrol together may offer a promising strategy for BC treatment.

## Linked entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099], TP53 (tumor protein p53) [NCBI Gene 7157], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207]
- **Chemicals:** arsenic trioxide (PubChem CID 14888), resveratrol (PubChem CID 5056)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}
- **Diseases:** TP53 (MESH:D009369), BC (MESH:D001943)
- **Chemicals:** ATO (MESH:D000077237), Resveratrol (MESH:D000077185)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12886575