Antonios-Periklis Panagiotopoulos
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Antonios-Periklis Panagiotopoulos has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Achilleas Mitrakas
Department of Radiotherapy/Oncology, University Hospital of Alexandroupolis, Democritus University of Thrace, 68100 Alexandroupolis, Greece
1 shared publication - Christina Nikolaidou
Laboratory of Pathology, Ippokrateio General Hospital of Thessaloniki, 54642 Thessaloniki, Greece
1 shared publication - Christina-Angelika Alexiadi
Laboratory of Histology-Embryology, Medical School, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece
1 shared publication - Gregory Trypsianis
Laboratory of Medical Statistics, School of Medicine, Democritus University of Thrace, 68100 Alexandroupolis, Greece
1 shared publication - Maria Lambropoulou
Laboratory of Histology-Embryology, Medical School, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece
1 shared publication - Olga Pagonopoulou
Laboratory of Neurophysiology, Medical School, Democritus University of Thrace, 68100 Alexandroupolis, Greece
1 shared publication
Latest Publications
- Open Access
- 5 August 2024
- Published by MDPI AG in Diagnostics
- Vol. 14 (15) , 1692
An Immunohistochemical Study of MAGE Proteins in Hepatocellular Carcinoma
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.
- 5 August 2024
- Published by MDPI AG in Diagnostics
- Vol. 14 (15) , 1692
Open AccessAn Immunohistochemical Study of MAGE Proteins in Hepatocellular Carcinoma
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.