Mapping MAGE-A4 expression in solid cancers for targeted therapies

Christin Habigt1, Sylvie Rottey2, Iben Spanggaard3

  • 1Roche Pharma Research and Early Development, Early Development Oncology, Roche Innovation Center Munich, Penzberg, Germany.

Frontiers in Oncology
|March 28, 2025
PubMed

Insights

Melanoma-associated antigen A4 (MAGE-A4) protein is expressed in 35% of solid tumors. High MAGE-A4 expression was found in adenoid cystic carcinoma, liposarcoma, and ovarian cancers, indicating potential therapeutic targets.

Area of Science:

  • Oncology
  • Immunology
  • Molecular Biology

Background:

  • Melanoma-associated antigen A4 (MAGE-A4) is a potential target for cancer immunotherapy.
  • Limited data exist on MAGE-A4 protein expression across diverse solid tumors.

Purpose of the Study:

  • To comprehensively assess MAGE-A4 protein expression in various solid cancers.
  • To identify cancer types with high MAGE-A4 prevalence for targeted anti-MAGE-A4 therapies.

Main Methods:

  • Immunohistochemistry (IHC) was used to analyze MAGE-A4 protein expression.
  • 200 patient samples with unresectable/metastatic solid cancers were examined.
  • The cohort was predominantly HLA-A*02:01 positive.

Main Results:

  • MAGE-A4 expression was detected in 35% of the overall cohort (69/200 patients).
  • Highest MAGE-A4 prevalence observed in adenoid cystic carcinoma (82%) and liposarcoma (67%).
  • Significant positivity also noted in ovarian serous/high-grade carcinoma (64%), squamous non-small cell lung cancer (64%), head and neck squamous cell carcinoma (60%), and esophageal cancer (54%).

Conclusions:

  • MAGE-A4 expression varies significantly across different cancer types.
  • Specific cancers show high MAGE-A4 prevalence, suggesting potential for stratified precision medicine approaches.
  • Further research into MAGE-A4's role in oncogenesis and treatment response is warranted.

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