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HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma

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 characteriz...

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Autores principales: Kren, Leos, Valkovsky, Ivo, Dolezel, Jan, Capak, Ivo, Pacik, Dalibor, Poprach, Alexandr, Lakomy, Radek, Redova, Martina, Fabian, Pavel, Krenova, Zdenka, Slaby, Ondrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408319/
https://www.ncbi.nlm.nih.gov/pubmed/22640987
http://dx.doi.org/10.1186/1746-1596-7-58
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author Kren, Leos
Valkovsky, Ivo
Dolezel, Jan
Capak, Ivo
Pacik, Dalibor
Poprach, Alexandr
Lakomy, Radek
Redova, Martina
Fabian, Pavel
Krenova, Zdenka
Slaby, Ondrej
author_facet Kren, Leos
Valkovsky, Ivo
Dolezel, Jan
Capak, Ivo
Pacik, Dalibor
Poprach, Alexandr
Lakomy, Radek
Redova, Martina
Fabian, Pavel
Krenova, Zdenka
Slaby, Ondrej
author_sort Kren, Leos
collection PubMed
description 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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spelling pubmed-34083192012-07-31 HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma Kren, Leos Valkovsky, Ivo Dolezel, Jan Capak, Ivo Pacik, Dalibor Poprach, Alexandr Lakomy, Radek Redova, Martina Fabian, Pavel Krenova, Zdenka Slaby, Ondrej Diagn Pathol Research 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 BioMed Central 2012-05-29 /pmc/articles/PMC3408319/ /pubmed/22640987 http://dx.doi.org/10.1186/1746-1596-7-58 Text en Copyright ©2012 Kren et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kren, Leos
Valkovsky, Ivo
Dolezel, Jan
Capak, Ivo
Pacik, Dalibor
Poprach, Alexandr
Lakomy, Radek
Redova, Martina
Fabian, Pavel
Krenova, Zdenka
Slaby, Ondrej
HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
title HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
title_full HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
title_fullStr HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
title_full_unstemmed HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
title_short HLA-G and HLA-E specific mRNAs connote opposite prognostic significance in renal cell carcinoma
title_sort hla-g and hla-e specific mrnas connote opposite prognostic significance in renal cell carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408319/
https://www.ncbi.nlm.nih.gov/pubmed/22640987
http://dx.doi.org/10.1186/1746-1596-7-58
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