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Suppression of basal, PMA-and IFN-α-, but not IFN-γ-induced expression of HLA class I in v-myc-transformed U-937 monoblasts
- Source :
- International Journal of Cancer. 52:759-765
- Publication Year :
- 1992
- Publisher :
- Wiley, 1992.
-
Abstract
- Recent studies have suggested that certain oncogenes, in particular members of the myc family, may be involved in the down-regulation of HLA class-I antigen expression observed in many types of tumor. We report that constitutive expression of an OK10 v-myc gene in human monoblastic U-937 cells results in a reduced expression of HLA class-I cell-surface expression and decreased levels of HLA class-I protein and mRNA. All class-I alleles, with the possible exception of HLA A3, were affected, as shown by one-dimensional isoelectric focusing (ID-IEF). Basal expression of the beta 2m chain was also reduced, although to a lesser extent. In addition, we show that the PMA-, and at least partially the IFN-alpha-induced increase in HLA class-I antigen expression, was inhibited in U-937-myc cells both at the protein and the mRNA level. In contrast, the response to IFN-gamma was normal. Another important difference in the response to IFN-gamma and alpha was that, while IFN-gamma abrogated the v-myc block of PMA-induced differentiation of U-937 cells, as previously reported, IFN-alpha did not. Our data show that v-myc negatively affects the regulation of both basal and inducible HLA class-I antigen expression.
- Subjects :
- Cancer Research
medicine.medical_treatment
Genes, myc
Monoblast
Human leukocyte antigen
Biology
Monocytes
Interferon-gamma
HLA-A3
Antigen
Antigens, CD
Tumor Cells, Cultured
medicine
Humans
Interferon gamma
RNA, Messenger
Alleles
Regulation of gene expression
Messenger RNA
CD11 Antigens
Histocompatibility Antigens Class I
Interferon-alpha
Cell Transformation, Viral
Molecular biology
Cytokine
Gene Expression Regulation
Oncology
Immunology
Tetradecanoylphorbol Acetate
Cell Division
medicine.drug
Subjects
Details
- ISSN :
- 10970215 and 00207136
- Volume :
- 52
- Database :
- OpenAIRE
- Journal :
- International Journal of Cancer
- Accession number :
- edsair.doi.dedup.....5d93046a9d49110c94e351b81a09f4b5
- Full Text :
- https://doi.org/10.1002/ijc.2910520515