Cross-Species Upregulation of MAGED2 in Liver Cancer Suggests a Role in Obesity-Driven Tumor Progression
Melanoma-associated antigens (MAGEs) are cancer-testis antigens (CTAs) aberrantly expressed in multiple cancer types, including hepatocellular carcinoma (HCC), and associated with aggressive phenotypes. Although MAGE proteins are widely studied as cancer immunotherapy targets, their roles in HCC and the regulation of their expression during liver pathogenesis in mouse models, including dietary effects, remain poorly understood. We analyzed <i>Mage</i> gene expression in liver tissues from 78 C3H/HeJ mice with chronic diet-induced obesity. While type I <i>MAGE</i> genes are frequently expressed in human HCC, we found no evidence of their expression in mouse liver tumors, suggesting species-specific regulation. In contrast, type II <i>Maged2</i>, previously reported to be upregulated in human HCC, was significantly increased in mouse liver tumors. Analysis of human HCC samples from The Cancer Genome Atlas (TCGA) database confirmed <i>MAGED2</i> upregulation and its association with patient prognosis. Together, these findings identify <i>MAGED2</i> as a conserved marker of liver cancer in both humans and mice and emphasize the importance of cross-species comparative approaches for selecting appropriate models and accurately interpreting results, particularly for CTAs, which often evolved recently and in a species-specific manner.
Authors
- Klementina Fon Tacer
- Farzana Yeasmin Popy
- Jorge Diaz-Riaño
- Denis Štepihar
- Yusuff Olayiwola
- Kaja Blagotinšek Cokan
- Benjamin Barr
- Tara Bayat
- Stephanie Myers
- Rebecca R. Florke Gee
- Damjana Rozman
- Lauren Gollahon
- Juan Sebastian Solano Gutierrez
Institutions
- Texas Tech University (US)
- University of Ljubljana (SI)
- Universidad de Los Andes (CO)
- Augusta University (US)
- BIA Separations (Slovenia) (SI)
- Labena (Slovenia) (SI)
- Amarillo College (US)
Publication Details
- Journal
- Current Issues in Molecular Biology
- Published
- 2026-01-27
- DOI
- https://doi.org/10.3390/cimb48020139
- Primary Topic
- Immunotherapy and Immune Responses
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Texas Tech University
- Directorate for Biological Sciences