Cargando…
The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model
OBJECTIVE: The objective of this study was to examine the impact of dehydrated human amnion/chorion membrane (dHACM) allografts on prostate and bladder cancer growth in the setting of residual disease and positive surgical margins. MATERIALS AND METHODS: A commercially available version of dHACM was...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444417/ https://www.ncbi.nlm.nih.gov/pubmed/30956688 http://dx.doi.org/10.1177/1756287219837771 |
_version_ | 1783408027876982784 |
---|---|
author | Alvim, Ricardo G. Hughes, Christopher Somma, Alexander Nagar, Karan K. Wong, Nathan C. La Rosa, Stephen Monette, Sebastien Kim, Kwanghee Coleman, Jonathan A. |
author_facet | Alvim, Ricardo G. Hughes, Christopher Somma, Alexander Nagar, Karan K. Wong, Nathan C. La Rosa, Stephen Monette, Sebastien Kim, Kwanghee Coleman, Jonathan A. |
author_sort | Alvim, Ricardo G. |
collection | PubMed |
description | OBJECTIVE: The objective of this study was to examine the impact of dehydrated human amnion/chorion membrane (dHACM) allografts on prostate and bladder cancer growth in the setting of residual disease and positive surgical margins. MATERIALS AND METHODS: A commercially available version of dHACM was used. Cytokines were identified and quantified, followed by comparative analysis of cell growth in two different human cell lines: prostate cancer (LNCaP) and bladder cancer (UM-UC-3), in vitro and in vivo. Tumor growth between the two groups, membrane versus no membrane implant, was compared and immunohistochemistry studies were conducted to quantify CD-31, Ki-67, and vimentin. A Student’s unpaired t-test was used to determine statistical significance. RESULTS: The UM-UC-3 and LNCaP cells grew quicker in medium plus 10% serum and dHACM extract than in the other media (p = 0.03). A total of 28 distinct cytokines were found in the extract, 11 of which had relatively high concentrations and are associated with prostate and bladder cancer tumor progression. In vivo LNCaP model, after 10 weeks, the median tumor volume in the membrane group was almost threefold larger than the partial resection alone (p = 0.01). Two weeks after resection, in the UM-UC-3 model, the membrane group reached fourfold larger than the partial resection without membrane group (p < 0.01). In both groups, the expression of CD-31 and Ki-67 markers were similar and showed no statistical significance (p > 0.05). It was only in the LNCaP tumors that vimentin expression was significantly higher in the group without membrane compared with the membrane group (p = 0.008). CONCLUSION: The use of dHACM after partial tumor resection is related to faster tumor relapse and growth in prostate and urothelial cancer in vivo models, showing a potential risk of rapid local recurrence in patients at high risk of positive margins. |
format | Online Article Text |
id | pubmed-6444417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-64444172019-04-05 The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model Alvim, Ricardo G. Hughes, Christopher Somma, Alexander Nagar, Karan K. Wong, Nathan C. La Rosa, Stephen Monette, Sebastien Kim, Kwanghee Coleman, Jonathan A. Ther Adv Urol Original Research OBJECTIVE: The objective of this study was to examine the impact of dehydrated human amnion/chorion membrane (dHACM) allografts on prostate and bladder cancer growth in the setting of residual disease and positive surgical margins. MATERIALS AND METHODS: A commercially available version of dHACM was used. Cytokines were identified and quantified, followed by comparative analysis of cell growth in two different human cell lines: prostate cancer (LNCaP) and bladder cancer (UM-UC-3), in vitro and in vivo. Tumor growth between the two groups, membrane versus no membrane implant, was compared and immunohistochemistry studies were conducted to quantify CD-31, Ki-67, and vimentin. A Student’s unpaired t-test was used to determine statistical significance. RESULTS: The UM-UC-3 and LNCaP cells grew quicker in medium plus 10% serum and dHACM extract than in the other media (p = 0.03). A total of 28 distinct cytokines were found in the extract, 11 of which had relatively high concentrations and are associated with prostate and bladder cancer tumor progression. In vivo LNCaP model, after 10 weeks, the median tumor volume in the membrane group was almost threefold larger than the partial resection alone (p = 0.01). Two weeks after resection, in the UM-UC-3 model, the membrane group reached fourfold larger than the partial resection without membrane group (p < 0.01). In both groups, the expression of CD-31 and Ki-67 markers were similar and showed no statistical significance (p > 0.05). It was only in the LNCaP tumors that vimentin expression was significantly higher in the group without membrane compared with the membrane group (p = 0.008). CONCLUSION: The use of dHACM after partial tumor resection is related to faster tumor relapse and growth in prostate and urothelial cancer in vivo models, showing a potential risk of rapid local recurrence in patients at high risk of positive margins. SAGE Publications 2019-03-29 /pmc/articles/PMC6444417/ /pubmed/30956688 http://dx.doi.org/10.1177/1756287219837771 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Alvim, Ricardo G. Hughes, Christopher Somma, Alexander Nagar, Karan K. Wong, Nathan C. La Rosa, Stephen Monette, Sebastien Kim, Kwanghee Coleman, Jonathan A. The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
title | The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
title_full | The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
title_fullStr | The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
title_full_unstemmed | The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
title_short | The potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
title_sort | potential risk of tumor progression after use of dehydrated human amnion/chorion membrane allograft in a positive margin resection model |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444417/ https://www.ncbi.nlm.nih.gov/pubmed/30956688 http://dx.doi.org/10.1177/1756287219837771 |
work_keys_str_mv | AT alvimricardog thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT hugheschristopher thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT sommaalexander thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT nagarkarank thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT wongnathanc thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT larosastephen thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT monettesebastien thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT kimkwanghee thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT colemanjonathana thepotentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT alvimricardog potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT hugheschristopher potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT sommaalexander potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT nagarkarank potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT wongnathanc potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT larosastephen potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT monettesebastien potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT kimkwanghee potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel AT colemanjonathana potentialriskoftumorprogressionafteruseofdehydratedhumanamnionchorionmembraneallograftinapositivemarginresectionmodel |