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CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding

In order to identify potential markers of renal cancer, the plasma membrane protein content of renal cell carcinoma (RCC)-derived cell lines was annotated using a proteomics process. One unusual protein identified at high levels in A498 and 786-O cells was CD70 (TNFSF7), a type II transmembrane rece...

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Autores principales: Adam, P J, Terrett, J A, Steers, G, Stockwin, L, Loader, J A, Fletcher, G C, Lu, L-S, Leach, B I, Mason, S, Stamps, A C, Boyd, R S, Pezzella, F, Gatter, K C, Harris, A L
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360640/
https://www.ncbi.nlm.nih.gov/pubmed/16892042
http://dx.doi.org/10.1038/sj.bjc.6603222
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author Adam, P J
Terrett, J A
Steers, G
Stockwin, L
Loader, J A
Fletcher, G C
Lu, L-S
Leach, B I
Mason, S
Stamps, A C
Boyd, R S
Pezzella, F
Gatter, K C
Harris, A L
author_facet Adam, P J
Terrett, J A
Steers, G
Stockwin, L
Loader, J A
Fletcher, G C
Lu, L-S
Leach, B I
Mason, S
Stamps, A C
Boyd, R S
Pezzella, F
Gatter, K C
Harris, A L
author_sort Adam, P J
collection PubMed
description In order to identify potential markers of renal cancer, the plasma membrane protein content of renal cell carcinoma (RCC)-derived cell lines was annotated using a proteomics process. One unusual protein identified at high levels in A498 and 786-O cells was CD70 (TNFSF7), a type II transmembrane receptor normally expressed on a subset of B, T and NK cells, where it plays a costimulatory role in immune cell activation. Immunohistochemical analysis of CD70 expression in multiple carcinoma types demonstrated strong CD70 staining in RCC tissues. Metastatic tissues from eight of 11 patients with clear cell RCC were positive for CD70 expression. Immunocytochemical analysis demonstrated that binding of an anti-CD70 antibody to CD70 endogenously expressed on the surface of A498 and 786-O cell lines resulted in the rapid internalisation of the antibody–receptor complex. Coincubation of the internalising anti-CD70 antibody with a saporin-conjugated secondary antibody before addition to A498 cells resulted in 50% cell killing. These data indicate that CD70 represents a potential target antigen for toxin-conjugated therapeutic antibody treatment of RCC.
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spelling pubmed-23606402009-09-10 CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding Adam, P J Terrett, J A Steers, G Stockwin, L Loader, J A Fletcher, G C Lu, L-S Leach, B I Mason, S Stamps, A C Boyd, R S Pezzella, F Gatter, K C Harris, A L Br J Cancer Molecular Diagnostics In order to identify potential markers of renal cancer, the plasma membrane protein content of renal cell carcinoma (RCC)-derived cell lines was annotated using a proteomics process. One unusual protein identified at high levels in A498 and 786-O cells was CD70 (TNFSF7), a type II transmembrane receptor normally expressed on a subset of B, T and NK cells, where it plays a costimulatory role in immune cell activation. Immunohistochemical analysis of CD70 expression in multiple carcinoma types demonstrated strong CD70 staining in RCC tissues. Metastatic tissues from eight of 11 patients with clear cell RCC were positive for CD70 expression. Immunocytochemical analysis demonstrated that binding of an anti-CD70 antibody to CD70 endogenously expressed on the surface of A498 and 786-O cell lines resulted in the rapid internalisation of the antibody–receptor complex. Coincubation of the internalising anti-CD70 antibody with a saporin-conjugated secondary antibody before addition to A498 cells resulted in 50% cell killing. These data indicate that CD70 represents a potential target antigen for toxin-conjugated therapeutic antibody treatment of RCC. Nature Publishing Group 2006-08-07 2006-08-01 /pmc/articles/PMC2360640/ /pubmed/16892042 http://dx.doi.org/10.1038/sj.bjc.6603222 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Adam, P J
Terrett, J A
Steers, G
Stockwin, L
Loader, J A
Fletcher, G C
Lu, L-S
Leach, B I
Mason, S
Stamps, A C
Boyd, R S
Pezzella, F
Gatter, K C
Harris, A L
CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
title CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
title_full CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
title_fullStr CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
title_full_unstemmed CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
title_short CD70 (TNFSF7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
title_sort cd70 (tnfsf7) is expressed at high prevalence in renal cell carcinomas and is rapidly internalised on antibody binding
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360640/
https://www.ncbi.nlm.nih.gov/pubmed/16892042
http://dx.doi.org/10.1038/sj.bjc.6603222
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