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Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients

BACKGROUND: A novel gammaretrovirus named xenotropic murine leukemia virus-related virus (XMRV) has been recently identified and found to have a prevalence of 40% in prostate tumor samples from American patients carrying a homozygous R462Q mutation in the RNaseL gene. This mutation impairs the funct...

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Autores principales: Hohn, Oliver, Krause, Hans, Barbarotto, Pia, Niederstadt, Lars, Beimforde, Nadine, Denner, Joachim, Miller, Kurt, Kurth, Reinhard, Bannert, Norbert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770519/
https://www.ncbi.nlm.nih.gov/pubmed/19835577
http://dx.doi.org/10.1186/1742-4690-6-92
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author Hohn, Oliver
Krause, Hans
Barbarotto, Pia
Niederstadt, Lars
Beimforde, Nadine
Denner, Joachim
Miller, Kurt
Kurth, Reinhard
Bannert, Norbert
author_facet Hohn, Oliver
Krause, Hans
Barbarotto, Pia
Niederstadt, Lars
Beimforde, Nadine
Denner, Joachim
Miller, Kurt
Kurth, Reinhard
Bannert, Norbert
author_sort Hohn, Oliver
collection PubMed
description BACKGROUND: A novel gammaretrovirus named xenotropic murine leukemia virus-related virus (XMRV) has been recently identified and found to have a prevalence of 40% in prostate tumor samples from American patients carrying a homozygous R462Q mutation in the RNaseL gene. This mutation impairs the function of the innate antiviral type I interferon pathway and is a known susceptibility factor for prostate cancer. Here, we attempt to measure the prevalence of XMRV in prostate cancer cases in Germany and determine whether an analogous association with the R462Q polymorphism exists. RESULTS: 589 prostate tumor samples were genotyped by real-time PCR with regard to the RNaseL mutation. DNA and RNA samples from these patients were screened for the presence of XMRV-specific gag sequences using a highly sensitive nested PCR and RT-PCR approach. Furthermore, 146 sera samples from prostate tumor patients were tested for XMRV Gag and Env antibodies using a newly developed ELISA assay. In agreement with earlier data, 12.9% (76 samples) were shown to be of the QQ genotype. However, XMRV specific sequences were detected at neither the DNA nor the RNA level. Consistent with this result, none of the sera analyzed from prostate cancer patients contained XMRV-specific antibodies. CONCLUSION: Our results indicate a much lower prevalence (or even complete absence) of XMRV in prostate tumor patients in Germany. One possible reason for this could be a geographically restricted incidence of XMRV infections.
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spelling pubmed-27705192009-10-30 Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients Hohn, Oliver Krause, Hans Barbarotto, Pia Niederstadt, Lars Beimforde, Nadine Denner, Joachim Miller, Kurt Kurth, Reinhard Bannert, Norbert Retrovirology Research BACKGROUND: A novel gammaretrovirus named xenotropic murine leukemia virus-related virus (XMRV) has been recently identified and found to have a prevalence of 40% in prostate tumor samples from American patients carrying a homozygous R462Q mutation in the RNaseL gene. This mutation impairs the function of the innate antiviral type I interferon pathway and is a known susceptibility factor for prostate cancer. Here, we attempt to measure the prevalence of XMRV in prostate cancer cases in Germany and determine whether an analogous association with the R462Q polymorphism exists. RESULTS: 589 prostate tumor samples were genotyped by real-time PCR with regard to the RNaseL mutation. DNA and RNA samples from these patients were screened for the presence of XMRV-specific gag sequences using a highly sensitive nested PCR and RT-PCR approach. Furthermore, 146 sera samples from prostate tumor patients were tested for XMRV Gag and Env antibodies using a newly developed ELISA assay. In agreement with earlier data, 12.9% (76 samples) were shown to be of the QQ genotype. However, XMRV specific sequences were detected at neither the DNA nor the RNA level. Consistent with this result, none of the sera analyzed from prostate cancer patients contained XMRV-specific antibodies. CONCLUSION: Our results indicate a much lower prevalence (or even complete absence) of XMRV in prostate tumor patients in Germany. One possible reason for this could be a geographically restricted incidence of XMRV infections. BioMed Central 2009-10-16 /pmc/articles/PMC2770519/ /pubmed/19835577 http://dx.doi.org/10.1186/1742-4690-6-92 Text en Copyright © 2009 Hohn 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
Hohn, Oliver
Krause, Hans
Barbarotto, Pia
Niederstadt, Lars
Beimforde, Nadine
Denner, Joachim
Miller, Kurt
Kurth, Reinhard
Bannert, Norbert
Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients
title Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients
title_full Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients
title_fullStr Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients
title_full_unstemmed Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients
title_short Lack of evidence for xenotropic murine leukemia virus-related virus(XMRV) in German prostate cancer patients
title_sort lack of evidence for xenotropic murine leukemia virus-related virus(xmrv) in german prostate cancer patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770519/
https://www.ncbi.nlm.nih.gov/pubmed/19835577
http://dx.doi.org/10.1186/1742-4690-6-92
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