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Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays
BACKGROUND: Adenocarcinoma is the most common type of non-small cell lung cancer and is frequently observed in non-smoking patients. Adenocarcinoma in-situ (formerly referred to as bronchioloalveolar carcinoma) is a subset of lung adenocarcinoma characterized by growth along alveolar septae without...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995318/ https://www.ncbi.nlm.nih.gov/pubmed/24642139 http://dx.doi.org/10.1186/1756-0500-7-160 |
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author | Linnerth-Petrik, Nicolle M Walsh, Scott R Bogner, Paul N Morrison, Carl Wootton, Sarah K |
author_facet | Linnerth-Petrik, Nicolle M Walsh, Scott R Bogner, Paul N Morrison, Carl Wootton, Sarah K |
author_sort | Linnerth-Petrik, Nicolle M |
collection | PubMed |
description | BACKGROUND: Adenocarcinoma is the most common type of non-small cell lung cancer and is frequently observed in non-smoking patients. Adenocarcinoma in-situ (formerly referred to as bronchioloalveolar carcinoma) is a subset of lung adenocarcinoma characterized by growth along alveolar septae without evidence of stromal, vascular, or pleural invasion, that disproportionately affects never-smokers, women, and Asians. Adenocarcinoma in-situ is morphologically and histologically similar to a contagious lung neoplasm of sheep called ovine pulmonary adenocarcinoma (OPA). OPA is caused by infection with the exogenous betaretrovirus, jaagsiekte sheep retrovirus (JSRV), whose envelope protein (Env) is a potent oncogene. Several studies have reported that a proportion of human lung adenocarcinomas are immunopositive for an antigen related to the Gag protein of JSRV, however other groups have been unable to verify these observations by PCR. METHODS: Here we examine human lung cancer tissue arrays (TA) for evidence of JSRV Env protein and DNA by immunohistochemical staining and PCR, respectively. RESULTS: Our results reveal that a subset of human lung cancers express an antigen that reacts with a JSRV Env-specific monoclonal antibody in immunohistochemistry and that exogenous JSRV-like env and gag sequences can be amplified from TA tumor samples, albeit inefficiently. CONCLUSIONS: While a causative role has not been established, these data suggest that a JSRV-like virus might infect humans. With next generation sequencing approaches, a JSRV-like virus in human lung cancers may be identified which could have profound implications for prevention, diagnosis and therapy. |
format | Online Article Text |
id | pubmed-3995318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39953182014-04-23 Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays Linnerth-Petrik, Nicolle M Walsh, Scott R Bogner, Paul N Morrison, Carl Wootton, Sarah K BMC Res Notes Research Article BACKGROUND: Adenocarcinoma is the most common type of non-small cell lung cancer and is frequently observed in non-smoking patients. Adenocarcinoma in-situ (formerly referred to as bronchioloalveolar carcinoma) is a subset of lung adenocarcinoma characterized by growth along alveolar septae without evidence of stromal, vascular, or pleural invasion, that disproportionately affects never-smokers, women, and Asians. Adenocarcinoma in-situ is morphologically and histologically similar to a contagious lung neoplasm of sheep called ovine pulmonary adenocarcinoma (OPA). OPA is caused by infection with the exogenous betaretrovirus, jaagsiekte sheep retrovirus (JSRV), whose envelope protein (Env) is a potent oncogene. Several studies have reported that a proportion of human lung adenocarcinomas are immunopositive for an antigen related to the Gag protein of JSRV, however other groups have been unable to verify these observations by PCR. METHODS: Here we examine human lung cancer tissue arrays (TA) for evidence of JSRV Env protein and DNA by immunohistochemical staining and PCR, respectively. RESULTS: Our results reveal that a subset of human lung cancers express an antigen that reacts with a JSRV Env-specific monoclonal antibody in immunohistochemistry and that exogenous JSRV-like env and gag sequences can be amplified from TA tumor samples, albeit inefficiently. CONCLUSIONS: While a causative role has not been established, these data suggest that a JSRV-like virus might infect humans. With next generation sequencing approaches, a JSRV-like virus in human lung cancers may be identified which could have profound implications for prevention, diagnosis and therapy. BioMed Central 2014-03-19 /pmc/articles/PMC3995318/ /pubmed/24642139 http://dx.doi.org/10.1186/1756-0500-7-160 Text en Copyright © 2014 Linnerth-Petrik 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 credited. |
spellingShingle | Research Article Linnerth-Petrik, Nicolle M Walsh, Scott R Bogner, Paul N Morrison, Carl Wootton, Sarah K Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
title | Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
title_full | Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
title_fullStr | Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
title_full_unstemmed | Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
title_short | Jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
title_sort | jaagsiekte sheep retrovirus detected in human lung cancer tissue arrays |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995318/ https://www.ncbi.nlm.nih.gov/pubmed/24642139 http://dx.doi.org/10.1186/1756-0500-7-160 |
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