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Metastatic phenotype in CWR22 prostate cancer xenograft following castration
BACKGROUND: CWR22 is a human xenograft model of primary prostate cancer (PCa) that is often utilized to study castration recurrent (CR) PCa. CWR22 recapitulates clinical response to androgen deprivation therapy (ADT), in that tumors regress in response to castration, but can recur after a period of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745026/ https://www.ncbi.nlm.nih.gov/pubmed/26642837 http://dx.doi.org/10.1002/pros.23127 |
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author | Seedhouse, Steven J. Affronti, Hayley C. Karasik, Ellen Gillard, Bryan M. Azabdaftari, Gissou Smiraglia, Dominic J. Foster, Barbara A. |
author_facet | Seedhouse, Steven J. Affronti, Hayley C. Karasik, Ellen Gillard, Bryan M. Azabdaftari, Gissou Smiraglia, Dominic J. Foster, Barbara A. |
author_sort | Seedhouse, Steven J. |
collection | PubMed |
description | BACKGROUND: CWR22 is a human xenograft model of primary prostate cancer (PCa) that is often utilized to study castration recurrent (CR) PCa. CWR22 recapitulates clinical response to androgen deprivation therapy (ADT), in that tumors regress in response to castration, but can recur after a period of time. METHODS: Two cohorts of mice, totaling 117 mice were implanted with CWR22, allowed to develop tumors, castrated by pellet removal and followed for a period of 32 and 50 weeks. Mice presenting with tumors >2.0 cm(3) at the primary site, moribund appearance, or palpable masses other than the primary tumor were sacrificed prior to the endpoint of the study. Tumor tissue, serum, and abnormal lesions were collected upon necropsy and analyzed by IHC, H&E, and PCR for presence of metastatic lesions arising from CWR22. RESULTS: Herein, we report that CWR22 progresses after castration from a primary, hormonal therapy‐naïve tumor to metastatic disease in 20% of castrated nude mice. Histological examination of CWR22 primary tumors revealed distinct pathologies that correlated with metastatic outcome after castration. CONCLUSION: This is the first report and characterization of spontaneous metastasis in the CWR22 model, thus, CWR22 is a bona‐fide model of clinical PCa representing the full progression from androgen‐sensitive, primary PCa to metastatic CR‐PCa. Prostate 76:359–368, 2016. © 2015 The Authors. The Prostate published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-4745026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47450262016-02-18 Metastatic phenotype in CWR22 prostate cancer xenograft following castration Seedhouse, Steven J. Affronti, Hayley C. Karasik, Ellen Gillard, Bryan M. Azabdaftari, Gissou Smiraglia, Dominic J. Foster, Barbara A. Prostate Original Articles BACKGROUND: CWR22 is a human xenograft model of primary prostate cancer (PCa) that is often utilized to study castration recurrent (CR) PCa. CWR22 recapitulates clinical response to androgen deprivation therapy (ADT), in that tumors regress in response to castration, but can recur after a period of time. METHODS: Two cohorts of mice, totaling 117 mice were implanted with CWR22, allowed to develop tumors, castrated by pellet removal and followed for a period of 32 and 50 weeks. Mice presenting with tumors >2.0 cm(3) at the primary site, moribund appearance, or palpable masses other than the primary tumor were sacrificed prior to the endpoint of the study. Tumor tissue, serum, and abnormal lesions were collected upon necropsy and analyzed by IHC, H&E, and PCR for presence of metastatic lesions arising from CWR22. RESULTS: Herein, we report that CWR22 progresses after castration from a primary, hormonal therapy‐naïve tumor to metastatic disease in 20% of castrated nude mice. Histological examination of CWR22 primary tumors revealed distinct pathologies that correlated with metastatic outcome after castration. CONCLUSION: This is the first report and characterization of spontaneous metastasis in the CWR22 model, thus, CWR22 is a bona‐fide model of clinical PCa representing the full progression from androgen‐sensitive, primary PCa to metastatic CR‐PCa. Prostate 76:359–368, 2016. © 2015 The Authors. The Prostate published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-12-08 2016-03 /pmc/articles/PMC4745026/ /pubmed/26642837 http://dx.doi.org/10.1002/pros.23127 Text en © 2015 The Authors. The Prostate published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Seedhouse, Steven J. Affronti, Hayley C. Karasik, Ellen Gillard, Bryan M. Azabdaftari, Gissou Smiraglia, Dominic J. Foster, Barbara A. Metastatic phenotype in CWR22 prostate cancer xenograft following castration |
title | Metastatic phenotype in CWR22 prostate cancer xenograft following castration |
title_full | Metastatic phenotype in CWR22 prostate cancer xenograft following castration |
title_fullStr | Metastatic phenotype in CWR22 prostate cancer xenograft following castration |
title_full_unstemmed | Metastatic phenotype in CWR22 prostate cancer xenograft following castration |
title_short | Metastatic phenotype in CWR22 prostate cancer xenograft following castration |
title_sort | metastatic phenotype in cwr22 prostate cancer xenograft following castration |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745026/ https://www.ncbi.nlm.nih.gov/pubmed/26642837 http://dx.doi.org/10.1002/pros.23127 |
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