Evidence map›Paper›PMID 41566414›Full record

ArticleBMC gastroenterology2026

Melanoma antigen genes A1 and A3 as predictors of treatment response and survival in HCV-associated hepatocellular carcinoma: a prospective study.

Hoda Elgamal, Dina Elhammady, Salwa M Abo El-Khair, Adel El-Badrawy, Amr Samir, Khaled Farid, Hatem El Alfy

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Article in BMC gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Hoda ElgamalTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Dina ElhammadyTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Salwa M Abo El-KhairMedical Biochemistry and Molecular Biology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Adel El-BadrawyDiagnostic and Interventional Radiology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Amr SamirTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt. dramrsamir@mans.edu.eg.
Khaled FaridTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Hatem El AlfyTropical Medicine Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHepatocellular carcinoma (HCC) accounts for approximately 90% of all primary liver cancers resulting in approximately 830,000 deaths in 2020, making HCC the sixth most common cancer globally. Several members of the Melanoma Antigen Gene (MAGE) family, such as MAGE-A1 and A3 genes of the MAGE I-A subfamily, are abnormally expressed in a variety of cancers including melanomas, colorectal cancer, non-small cell lung cancer, gliomas, HCC, prostate, and breast cancers. In addition, they have been linked to tumor stemness and, therefore, may predict therapeutic response and prognosis. AIM OF THE STUDY: To investigate the expression pattern of MAGE-A1 and A3 genes in HCC patients and to evaluate their prognostic value. SUBJECTS AND

methodsThis prospective four-year case-control study was conducted from 2020 to 2024 on 95 subjects classified into three groups. Group (A): Fifty patients with HCC developed on top of hepatitis C virus (HCV) - induced liver cirrhosis, Group (B): 30 patients with post-HCV liver cirrhosis and Group (C): 15 healthy control subjects. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to evaluate the expression of MAGE-A1 and A3 genes in peripheral blood sample after peripheral blood mononuclear cells (PBMCs) isolation. Patients were followed up over 2 years duration for assessment of treatment response.

resultsAt cutoff levels 11.54 and 11.39 MAGE-A1 and MAGE-A3, respectively, could distinguish HCC from liver cirrhosis with area under the curve (AUC) of 0.781 and 0.966, respectively (P ≤ 0.001). Regarding treatment response, MAGE-A1 and A3 showed significantly higher expression in patients with progressive disease (16.16 and 17.79, respectively) compared to complete response patients (9.21 and 13.25, respectively). Finally, when assessing overall survival (OS) in HCC patients multivariate analysis showed that independent factors for shorter OS were increased MAGE-A1 (HR: 9.407, P: 0.048), high MAGE-A3 (HR: 9.199, P: 0.042) and elevation of both alpha fetoprotein (AFP) and MAGE-A3 (HR: 10.681, P: 0.039).

conclusionMAGE-A1 and A3 genes can be used as diagnostic and prognostic markers in HCC patients predicting therapeutic response and overall survival.

Indexed as

Antigens, NeoplasmCarcinoma, HepatocellularLiver NeoplasmsMelanoma-Specific AntigensNeoplasm ProteinsAdultAgedBiomarkers, TumorCase-Control StudiesFemaleHumansLiver CirrhosisMaleMiddle AgedPrognosisProspective StudiesAntigens, NeoplasmBiomarkers, TumorMAGEA1 protein, humanMAGEA3 protein, humanMelanoma-Specific AntigensNeoplasm ProteinsHCCMAGE genes

Identifiers

PMID41566414
PMCPMC12836994

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