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High frequency of expression of MAGE genes in human hepatocellular carcinoma
- Source :
- Liver International. 19:110-114
- Publication Year :
- 1999
- Publisher :
- Wiley, 1999.
-
Abstract
- Aims/background Activation of human MAGE genes leads to the expression of a set of tumor rejection antigens, which are recognized by cytotoxic T lymphocytes. The antigens may become the targets of immunotherapy. The expression of MAGE genes was originally found in, but is not restricted, to melanomas. The aim of this study was to investigate the expression of MAGE genes in human hepatocellular carcinomas. Methods The expression of MAGE-1, -2, -3, -4 genes in tumorous and corresponding non-tumorous liver tissue was studied using a reverse-transcription polymerase chain reaction. Results In the 50 hepatocellular carcinomas studied, MAGE-1, -2, -3, -4 mRNA expression was detected in 23 (46%), 17 (34%), 21 (42%) and 8 (16%), respectively. Seventy-four percent of the hepatocellular carcinomas expressed at least one of the MAGE genes. MAGE mRNAs were not detected in the corresponding non-tumor liver tissues. MAGE gene expression was not significantly correlated with clinicopathological factors. Conclusions The MAGE genes are expressed in a high percentage of hepatocellular carcinomas; the MAGE gene products are potential targets for tumor-specific immunotherapy.
- Subjects :
- Adult
Male
endocrine system
Carcinoma, Hepatocellular
medicine.medical_treatment
Gene Expression
Biology
law.invention
Antigen
Antigens, Neoplasm
law
Gene expression
Biomarkers, Tumor
medicine
Humans
Cytotoxic T cell
neoplasms
Gene
Polymerase chain reaction
Aged
Hepatology
Liver Neoplasms
Immunotherapy
Middle Aged
medicine.disease
Neoplasm Proteins
Hepatocellular carcinoma
Immunology
Cancer research
Female
Melanoma-Specific Antigens
Subjects
Details
- ISSN :
- 14783231 and 14783223
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Liver International
- Accession number :
- edsair.doi.dedup.....3a6cd417c3d3a101c7622a168255f232
- Full Text :
- https://doi.org/10.1111/j.1478-3231.1999.tb00019.x