Cargando…
Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression
BACKGROUND: Hyaluronic acid is a prognostic factor in ovarian cancers. It is also a component of Hyaluronic Acid-Carboxymethyl Cellulose (HA-CMC) barrier, an anti-adhesion membrane widely used during abdominal surgeries in particular for ovarian carcinosis. 70% of patients who undergo ovarian surger...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996858/ https://www.ncbi.nlm.nih.gov/pubmed/24739440 http://dx.doi.org/10.1186/1757-2215-7-40 |
_version_ | 1782313106605604864 |
---|---|
author | Picaud, Laetitia Thibault, Benoît Mery, Eliane Ouali, Monia Martinez, Alejandra Delord, Jean-Pierre Couderc, Bettina Ferron, Gwenael |
author_facet | Picaud, Laetitia Thibault, Benoît Mery, Eliane Ouali, Monia Martinez, Alejandra Delord, Jean-Pierre Couderc, Bettina Ferron, Gwenael |
author_sort | Picaud, Laetitia |
collection | PubMed |
description | BACKGROUND: Hyaluronic acid is a prognostic factor in ovarian cancers. It is also a component of Hyaluronic Acid-Carboxymethyl Cellulose (HA-CMC) barrier, an anti-adhesion membrane widely used during abdominal surgeries in particular for ovarian carcinosis. 70% of patients who undergo ovarian surgery will relapse due to the persistence of cancer cells. This study’s objective was to determine the oncological risk from use of this material, in the presence of residual disease, despite the benefit gained by it decreasing post-surgical adhesions in order to provide an unambiguous assessment of its appropriateness for use in ovarian surgical management. METHODS: We assessed the effects of HA-CMC barrier on the in vitro proliferation of human ovarian tumor cell lines (OVCAR-3, IGROV-1 and SKOV-3). We next evaluated, in vivo in nude mice, the capacity of this biomaterial to regulate the tumor progression of subcutaneous and intraperitoneal models of ovarian tumor xenografts. RESULTS: We showed that HA-CMC barrier does not increase in vitro proliferation of ovarian cancer cell lines compared to control. In vivo, HA-CMC barrier presence with subcutaneous xenografts induced neither an increase in tumor volume nor cell proliferation (Ki67 and mitotic index). With the exception of an increased murine carcinosis score in peritoneum, the presence of HA-CMC barrier with intraperitoneal xenografts modified neither macro nor microscopic tumor growth. Finally, protein analysis of survival (Akt), proliferation (ERK) and adhesion (FAK) pathways highlighted no activation on the xenografts imputable to HA-CMC barrier. CONCLUSIONS: For the most part, our results support the lack of tumor progression activation due to HA-CMC barrier. We conclude that the benefits gained from using HA-CMC barrier membrane during ovarian cancer surgeries seem to outweigh the potential oncological risks. |
format | Online Article Text |
id | pubmed-3996858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39968582014-05-07 Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression Picaud, Laetitia Thibault, Benoît Mery, Eliane Ouali, Monia Martinez, Alejandra Delord, Jean-Pierre Couderc, Bettina Ferron, Gwenael J Ovarian Res Research BACKGROUND: Hyaluronic acid is a prognostic factor in ovarian cancers. It is also a component of Hyaluronic Acid-Carboxymethyl Cellulose (HA-CMC) barrier, an anti-adhesion membrane widely used during abdominal surgeries in particular for ovarian carcinosis. 70% of patients who undergo ovarian surgery will relapse due to the persistence of cancer cells. This study’s objective was to determine the oncological risk from use of this material, in the presence of residual disease, despite the benefit gained by it decreasing post-surgical adhesions in order to provide an unambiguous assessment of its appropriateness for use in ovarian surgical management. METHODS: We assessed the effects of HA-CMC barrier on the in vitro proliferation of human ovarian tumor cell lines (OVCAR-3, IGROV-1 and SKOV-3). We next evaluated, in vivo in nude mice, the capacity of this biomaterial to regulate the tumor progression of subcutaneous and intraperitoneal models of ovarian tumor xenografts. RESULTS: We showed that HA-CMC barrier does not increase in vitro proliferation of ovarian cancer cell lines compared to control. In vivo, HA-CMC barrier presence with subcutaneous xenografts induced neither an increase in tumor volume nor cell proliferation (Ki67 and mitotic index). With the exception of an increased murine carcinosis score in peritoneum, the presence of HA-CMC barrier with intraperitoneal xenografts modified neither macro nor microscopic tumor growth. Finally, protein analysis of survival (Akt), proliferation (ERK) and adhesion (FAK) pathways highlighted no activation on the xenografts imputable to HA-CMC barrier. CONCLUSIONS: For the most part, our results support the lack of tumor progression activation due to HA-CMC barrier. We conclude that the benefits gained from using HA-CMC barrier membrane during ovarian cancer surgeries seem to outweigh the potential oncological risks. BioMed Central 2014-04-16 /pmc/articles/PMC3996858/ /pubmed/24739440 http://dx.doi.org/10.1186/1757-2215-7-40 Text en Copyright © 2014 Picaud et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Picaud, Laetitia Thibault, Benoît Mery, Eliane Ouali, Monia Martinez, Alejandra Delord, Jean-Pierre Couderc, Bettina Ferron, Gwenael Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
title | Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
title_full | Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
title_fullStr | Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
title_full_unstemmed | Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
title_short | Evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
title_sort | evaluation of the effects of hyaluronic acid-carboxymethyl cellulose barrier on ovarian tumor progression |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996858/ https://www.ncbi.nlm.nih.gov/pubmed/24739440 http://dx.doi.org/10.1186/1757-2215-7-40 |
work_keys_str_mv | AT picaudlaetitia evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT thibaultbenoit evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT meryeliane evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT oualimonia evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT martinezalejandra evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT delordjeanpierre evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT coudercbettina evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression AT ferrongwenael evaluationoftheeffectsofhyaluronicacidcarboxymethylcellulosebarrieronovariantumorprogression |