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NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma
Background: Novel immune therapies targeting tumor specific antigens are being developed. Our purpose was to determine expression of the cancer testes antigen NY-ESO-1 in renal cell carcinoma (RCC), as NY-ESO-1 targeting approaches, particularly adoptive cell therapy, have not been evaluated in this...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170640/ https://www.ncbi.nlm.nih.gov/pubmed/24970819 |
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author | Giesen, Eva Jilaveanu, Lucia B. Parisi, Fabio Kluger, Yuval Camp, Robert L. Kluger, Harriet M. |
author_facet | Giesen, Eva Jilaveanu, Lucia B. Parisi, Fabio Kluger, Yuval Camp, Robert L. Kluger, Harriet M. |
author_sort | Giesen, Eva |
collection | PubMed |
description | Background: Novel immune therapies targeting tumor specific antigens are being developed. Our purpose was to determine expression of the cancer testes antigen NY-ESO-1 in renal cell carcinoma (RCC), as NY-ESO-1 targeting approaches, particularly adoptive cell therapy, have not been evaluated in this disease. Methods: We employed tissue microarrays containing >300 unique RCC cases and adjacent benign renal tissue to determine NY-ESO-1 expression using a quantitative immunofluorescence method. In addition, we studied NY-ESO-1 expression in 35 matched primary and metastatic RCC specimens to assess concordance between different tumor sites. Results: NY-ESO-1 was highly expressed in a subset of RCCs. Expression in primary RCC specimens was significantly higher than adjacent normal renal tissue (P<0.0001) and higher in clear cell carcinomas than papillary RCC (P<0.0001). Expression levels in metastatic specimens were higher than in matched primary samples (P=0.0018), and the correlation between the two sites was modest (χ(2)=3.5, p=0.06). Conclusions: Aberrant NY-ESO-1 expression seen in clear cell RCC suggests that NY-ESO-1 targeting approaches should be studied in this disease. Expression is higher in metastatic sites, and discordance between primary and metastatic sites in some patients suggests that patient selection for these therapies should be based on expression in metastatic rather than nephrectomy specimens. |
format | Online Article Text |
id | pubmed-4170640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41706402014-09-22 NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma Giesen, Eva Jilaveanu, Lucia B. Parisi, Fabio Kluger, Yuval Camp, Robert L. Kluger, Harriet M. Oncotarget Clinical Research Paper Background: Novel immune therapies targeting tumor specific antigens are being developed. Our purpose was to determine expression of the cancer testes antigen NY-ESO-1 in renal cell carcinoma (RCC), as NY-ESO-1 targeting approaches, particularly adoptive cell therapy, have not been evaluated in this disease. Methods: We employed tissue microarrays containing >300 unique RCC cases and adjacent benign renal tissue to determine NY-ESO-1 expression using a quantitative immunofluorescence method. In addition, we studied NY-ESO-1 expression in 35 matched primary and metastatic RCC specimens to assess concordance between different tumor sites. Results: NY-ESO-1 was highly expressed in a subset of RCCs. Expression in primary RCC specimens was significantly higher than adjacent normal renal tissue (P<0.0001) and higher in clear cell carcinomas than papillary RCC (P<0.0001). Expression levels in metastatic specimens were higher than in matched primary samples (P=0.0018), and the correlation between the two sites was modest (χ(2)=3.5, p=0.06). Conclusions: Aberrant NY-ESO-1 expression seen in clear cell RCC suggests that NY-ESO-1 targeting approaches should be studied in this disease. Expression is higher in metastatic sites, and discordance between primary and metastatic sites in some patients suggests that patient selection for these therapies should be based on expression in metastatic rather than nephrectomy specimens. Impact Journals LLC 2014-06-13 /pmc/articles/PMC4170640/ /pubmed/24970819 Text en Copyright: © 2014 Giesen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Giesen, Eva Jilaveanu, Lucia B. Parisi, Fabio Kluger, Yuval Camp, Robert L. Kluger, Harriet M. NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma |
title | NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma |
title_full | NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma |
title_fullStr | NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma |
title_full_unstemmed | NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma |
title_short | NY-ESO-1 as a potential immunotherapeutic target in renal cell carcinoma |
title_sort | ny-eso-1 as a potential immunotherapeutic target in renal cell carcinoma |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170640/ https://www.ncbi.nlm.nih.gov/pubmed/24970819 |
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