Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Giesen, Eva, Jilaveanu, Lucia B., Parisi, Fabio, Kluger, Yuval, Camp, Robert L., Kluger, Harriet M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170640/
https://www.ncbi.nlm.nih.gov/pubmed/24970819
_version_ 1782335841035616256
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
work_keys_str_mv AT gieseneva nyeso1asapotentialimmunotherapeutictargetinrenalcellcarcinoma
AT jilaveanuluciab nyeso1asapotentialimmunotherapeutictargetinrenalcellcarcinoma
AT parisifabio nyeso1asapotentialimmunotherapeutictargetinrenalcellcarcinoma
AT klugeryuval nyeso1asapotentialimmunotherapeutictargetinrenalcellcarcinoma
AT camprobertl nyeso1asapotentialimmunotherapeutictargetinrenalcellcarcinoma
AT klugerharrietm nyeso1asapotentialimmunotherapeutictargetinrenalcellcarcinoma