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Updated: May 10, 2026

MAME Models for 4D Live-cell Imaging of Tumor: Microenvironment Interactions that Impact Malignant Progression
Published on: February 17, 2012
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.
Abstract:
Melanoma-associated antigen A4 (MAGE-A4) is a promising target for anticancer therapy. However, limited contemporary data are available on the details of MAGE-A4 protein expression in different cancer types. In this study, the protein expression of MAGE-A4 is comprehensively studied in patients with unresectable and/or metastatic solid cancers to identify indications of the highest unmet medical need for anti-MAGE-A4 therapy. FFPE tumor sections from 200 patients, predominantly HLA-A*02:01 positive (n = 193), were examined using immunohistochemistry (IHC) to detect MAGE-A4 expression. The patient cohort comprised various cancer types to pinpoint differences in the prevalence and intensity of MAGE-A4 positivity. MAGE-A4 expression was observed in 35% (69 patients) of the overall cohort. Certain cancer types exhibited notably higher frequencies of MAGE-A4 positivity. Specifically, adenoid cystic carcinoma demonstrated the highest prevalence at 82%, followed by liposarcoma at 67%. Ovarian serous/high-grade carcinoma showed a 64% positivity rate, identical to that observed in squamous non-small cell lung cancer (NSCLC). Head and neck squamous cell carcinoma (HNSCC) presented a 60% prevalence, while esophageal cancer had a 54% prevalence of MAGE-A4 expression. These data highlight the variability of MAGE-A4 expression across different cancer types and underscore its relevance as a potential target of novel precision medicines. The significant presence of MAGE-A4 in specific cancers suggests potential for stratified therapeutic approaches and warrants further investigation into its role in oncogenesis and treatment response.
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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