# Male Breast Cancer: Epidemiology, Diagnosis, Molecular Mechanisms, Therapeutics, and Future Prospective

**Authors:** Ashok Kumar Sah, Ranjay Kumar Choudhary, Velilyaeva Alie Sabrievna, Karomatov Inomdzhon Dzhuraevich, Anass M. Abbas, Manar G. Shalabi, Nadeem Ahmad Siddique, Raji Rubayyi Alshammari, Navjyot Trivedi, Rabab H. Elshaikh

PMC · DOI: 10.32604/or.2025.068238 · Oncology Research · 2025-12-30

## TL;DR

Male breast cancer is rare but increasing, with unique risk factors and challenges in diagnosis and treatment, requiring tailored approaches for better outcomes.

## Contribution

The paper provides a comprehensive overview of MBC, highlighting molecular mechanisms and emerging therapies specific to men.

## Key findings

- MBC is often diagnosed late due to lack of screening and presents with ER-positive and HER2-negative features.
- Risk factors include BRCA1/2 mutations, hormonal imbalances, and lifestyle factors like obesity and alcohol use.
- Emerging therapies like CDK4/6 and PARP inhibitors, along with AI and precision medicine, offer new treatment prospects.

## Abstract

Male breast cancer (MBC) is rare, representing 0.5%–1% of all breast cancers, but its incidence is increasing due to improved diagnostics and awareness. MBC typically presents in older men, is human epidermal growth factor receptor 2 (HER2)-negative and estrogen receptor (ER)-positive, and lacks routine screening, leading to delayed diagnosis and advanced disease. Major risk factors include hormonal imbalance, radiation exposure, obesity, alcohol use, and Breast Cancer Gene 1 and 2 (BRCA1/2) mutations. Clinically, it may resemble gynecomastia but usually appears as a unilateral, painless mass or nipple discharge. Advances in imaging and liquid biopsy have enhanced early detection. Molecular mechanisms involve hormonal signaling, HER2/epidermal growth factor receptor (EGFR) pathways, tumor suppressor gene alterations, and epigenetic changes. While standard treatments mirror those for female breast cancer, emerging options such as cyclin-dependent kinase 4 and 6 (CDK4/6), and poly(ADP-ribose) polymerase (PARP) inhibitors, immunotherapy, and precision medicine are reshaping management. Incorporating artificial intelligence, molecular profiling, and male-specific clinical trials is essential to improve outcomes and bridge current diagnostic and therapeutic gaps.

## Linked entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672], BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675]
- **Proteins:** ERBB2 (erb-b2 receptor tyrosine kinase 2), EREG (epiregulin), EGFR (epidermal growth factor receptor)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142] {aka ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** obesity (MESH:D009765), MBC (MESH:D018567), tumor (MESH:D009369), gynecomastia (MESH:D006177), breast cancers (MESH:D001943)
- **Chemicals:** alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12774558/full.md

## References

152 references — full list in the complete paper: https://tomesphere.com/paper/PMC12774558/full.md

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Source: https://tomesphere.com/paper/PMC12774558