An Immunohistochemical Study of MAGE Proteins in Hepatocellular Carcinoma.

HCC MAGE family MAGE-C1 MAGE-C2 hepatocellular carcinoma

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
05 Aug 2024
Historique:
received: 12 06 2024
revised: 22 07 2024
accepted: 26 07 2024
medline: 10 8 2024
pubmed: 10 8 2024
entrez: 10 8 2024
Statut: epublish

Résumé

Hepatocellular carcinoma (HCC) is one the most common primary malignancies with high mortality and morbidity. The melanoma-associated antigen (MAGE) gene family includes several genes that are highly expressed in numerous human cancers, making many of them part of the cancer-testis antigen (CTA) family. MAGE-C1 is expressed in various malignancies but is absent in normal cells, except for the male germ line. Its presence is associated with a worse prognosis, increased tumor aggressiveness, and lymph node invasion. Similarly, MAGE-C2 is linked to the development of various malignant tumors. Despite these associations, the roles and mechanisms of MAGE-C1/MAGE-C2 in HCC remain unclear. This study aimed to evaluate the expression of MAGE-C1 and MAGE-C2 in HCC and correlate it with clinicohistological characteristics. Our findings indicated that MAGE-C1 expression is associated with a higher number of nodules, elevated AFP levels, HBV or HCV positivity, older age, male sex, and lymph node invasion. MAGE-C2 expression was correlated with these characteristics and the presence of cirrhosis. These results align with the limited literature, which suggests a correlation between MAGE expression and older age and HBV infection. Consequently, our study suggests that MAGE-C1 and MAGE-C2 are promising novel biomarkers for prognosis and potential therapeutic targets in HCC.

Identifiants

pubmed: 39125568
pii: diagnostics14151692
doi: 10.3390/diagnostics14151692
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Stylianos Tologkos (S)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Vasiliki Papadatou (V)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Achilleas G Mitrakas (AG)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Olga Pagonopoulou (O)

Laboratory of Neurophysiology, Medical School, Democritus University of Thrace, 68132 Alexandroupolis, Greece.

Grigorios Tripsianis (G)

Laboratory of Medical Statistics, Medical School, Democritus University of Thrace, 68132 Alexandroupolis, Greece.

Triantafyllos Alexiadis (T)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Christina-Angelika Alexiadi (CA)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Antonios-Periklis Panagiotopoulos (AP)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Christina Nikolaidou (C)

Laboratory of Pathology, Ippokrateio General Hospital of Thessaloniki, 54642 Thessaloniki, Greece.

Maria Lambropoulou (M)

Laboratory of Histology-Embryology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece.

Classifications MeSH