HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
Language English Country Great Britain, England Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22640987
PubMed Central
PMC3408319
DOI
10.1186/1746-1596-7-58
PII: 1746-1596-7-58
Knihovny.cz E-resources
- MeSH
- HLA-E Antigens MeSH
- Adult MeSH
- HLA-G Antigens biosynthesis genetics MeSH
- Immunohistochemistry MeSH
- Kaplan-Meier Estimate MeSH
- Carcinoma, Renal Cell immunology metabolism mortality MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger analysis MeSH
- Histocompatibility Antigens Class I biosynthesis genetics MeSH
- Biomarkers, Tumor analysis MeSH
- Kidney Neoplasms immunology metabolism mortality MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Disease-Free Survival MeSH
- Prognosis MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- HLA-G Antigens MeSH
- RNA, Messenger MeSH
- Histocompatibility Antigens Class I MeSH
- Biomarkers, Tumor MeSH
BACKGROUND: Renal cell carcinoma (RCC) is characterized by its resistance to radiotherapy and/or chemotherapy. On the other hand, it is an immunogenic tumor - it is able to stimulate antitumor responses. A prognostic significance of HLA-G expression by neoplastic cells in RCC is not well characterized; significance HLA-E expression in RCC is not characterized at all. METHODS: In our study, we evaluated the expression of HLA-G and HLA-E specific mRNA transcripts produced by neoplastic cells in 38 cases of RCC and in 10 samples of normal kidney parenchyma. The results were statistically correlated with various clinico-pathological parameters. RESULTS: We confirmed that HLA-G is downregulated in normal kidney tissue; if it is up-regulated in RCC, then it is connected to worse prognosis. On the other hand, HLA-E mRNA transcripts were present in both normal kidney tissue and RCC and their increasing concentrations counterintuitively carried better prognosis, more favorable pT stage and lower nuclear Fuhrmann's grade. CONCLUSION: Considering the fact that there is known aberrant activation of HLA-G and HLA-E expression by interferons, identification of HLA-G and HLA-E status could contribute to better selection of RCC patients who could possibly benefit from more tailored neoadjuvant biological/immunological therapy. Thus, these molecules could represent useful prognostic biomarkers in RCC, and the expression of both these molecules in RCC deserves further study. THE VIRTUAL: Slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/7383071387016614.
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