Cargando…
The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases
Rationale: Patients with colorectal cancer die mainly due to liver metastases (CRC-LM). Although the tumor microenvironment (TME) plays an important role in tumor development and therapeutic response, our understanding of the individual TME components, especially cancer-associated fibroblasts (CAFs)...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691344/ https://www.ncbi.nlm.nih.gov/pubmed/36438498 http://dx.doi.org/10.7150/thno.72853 |
_version_ | 1784837020684648448 |
---|---|
author | Giguelay, Ambre Turtoi, Evgenia Khelaf, Lakhdar Tosato, Guillaume Dadi, Ikrame Chastel, Tommy Poul, Marie-Alix Pratlong, Marine Nicolescu, Stefan Severac, Dany Adenis, Antoine Sgarbura, Olivia Carrère, Sébastien Rouanet, Philippe Quenet, François Ychou, Marc Pourquier, Didier Colombo, Pierre-Emmanuel Turtoi, Andrei Colinge, Jacques |
author_facet | Giguelay, Ambre Turtoi, Evgenia Khelaf, Lakhdar Tosato, Guillaume Dadi, Ikrame Chastel, Tommy Poul, Marie-Alix Pratlong, Marine Nicolescu, Stefan Severac, Dany Adenis, Antoine Sgarbura, Olivia Carrère, Sébastien Rouanet, Philippe Quenet, François Ychou, Marc Pourquier, Didier Colombo, Pierre-Emmanuel Turtoi, Andrei Colinge, Jacques |
author_sort | Giguelay, Ambre |
collection | PubMed |
description | Rationale: Patients with colorectal cancer die mainly due to liver metastases (CRC-LM). Although the tumor microenvironment (TME) plays an important role in tumor development and therapeutic response, our understanding of the individual TME components, especially cancer-associated fibroblasts (CAFs), remains limited. Methods: We analyzed CRC-LM CAFs and cancer cells by single-cell transcriptomics and used bioinformatics for data analysis and integration with related available single-cell and bulk transcriptomic datasets. We validated key findings by RT-qPCR, western blotting, and immunofluorescence. Results: By single-cell transcriptomic analysis of 4,397 CAFs from six CRC-LM samples, we identified two main CAF populations, contractile CAFs and extracellular matrix (ECM)-remodeling/pro-angiogenic CAFs, and four subpopulations with distinct phenotypes. We found that ECM-remodeling/pro-angiogenic CAFs derive from portal resident fibroblasts. They associate with areas of strong desmoplastic reaction and Wnt signaling in low-proliferating tumor cells engulfed in a stiff extracellular matrix. By integrating public single-cell primary liver tumor data, we propose a model to explain how different liver malignancies recruit CAFs of different origins to this organ. Lastly, we found that LTBP2 plays an important role in modulating collagen biosynthesis, ECM organization, and adhesion pathways. We developed fully human antibodies against LTBP2 that depleted LTBP2+ CAFs in vitro. Conclusion: This study complements recent reports on CRC-LM CAF heterogeneity at the single-cell resolution. The number of sequenced CAFs was more than one order of magnitude larger compared to existing data. LTBP2 targeting by antibodies might create opportunities to deplete ECM-remodeling CAFs in CRC-LMs. This might be combined with other therapies, e.g., anti-angiogenic compounds as already done in CRC. Moreover, we showed that in intrahepatic cholangiocarcinoma, in which ECM-remodeling CAF proportion is similar to that of CRC-LM, several genes expressed by ECM-remodeling CAFs, such as LTBP2, were associated with survival. |
format | Online Article Text |
id | pubmed-9691344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-96913442022-11-25 The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases Giguelay, Ambre Turtoi, Evgenia Khelaf, Lakhdar Tosato, Guillaume Dadi, Ikrame Chastel, Tommy Poul, Marie-Alix Pratlong, Marine Nicolescu, Stefan Severac, Dany Adenis, Antoine Sgarbura, Olivia Carrère, Sébastien Rouanet, Philippe Quenet, François Ychou, Marc Pourquier, Didier Colombo, Pierre-Emmanuel Turtoi, Andrei Colinge, Jacques Theranostics Research Paper Rationale: Patients with colorectal cancer die mainly due to liver metastases (CRC-LM). Although the tumor microenvironment (TME) plays an important role in tumor development and therapeutic response, our understanding of the individual TME components, especially cancer-associated fibroblasts (CAFs), remains limited. Methods: We analyzed CRC-LM CAFs and cancer cells by single-cell transcriptomics and used bioinformatics for data analysis and integration with related available single-cell and bulk transcriptomic datasets. We validated key findings by RT-qPCR, western blotting, and immunofluorescence. Results: By single-cell transcriptomic analysis of 4,397 CAFs from six CRC-LM samples, we identified two main CAF populations, contractile CAFs and extracellular matrix (ECM)-remodeling/pro-angiogenic CAFs, and four subpopulations with distinct phenotypes. We found that ECM-remodeling/pro-angiogenic CAFs derive from portal resident fibroblasts. They associate with areas of strong desmoplastic reaction and Wnt signaling in low-proliferating tumor cells engulfed in a stiff extracellular matrix. By integrating public single-cell primary liver tumor data, we propose a model to explain how different liver malignancies recruit CAFs of different origins to this organ. Lastly, we found that LTBP2 plays an important role in modulating collagen biosynthesis, ECM organization, and adhesion pathways. We developed fully human antibodies against LTBP2 that depleted LTBP2+ CAFs in vitro. Conclusion: This study complements recent reports on CRC-LM CAF heterogeneity at the single-cell resolution. The number of sequenced CAFs was more than one order of magnitude larger compared to existing data. LTBP2 targeting by antibodies might create opportunities to deplete ECM-remodeling CAFs in CRC-LMs. This might be combined with other therapies, e.g., anti-angiogenic compounds as already done in CRC. Moreover, we showed that in intrahepatic cholangiocarcinoma, in which ECM-remodeling CAF proportion is similar to that of CRC-LM, several genes expressed by ECM-remodeling CAFs, such as LTBP2, were associated with survival. Ivyspring International Publisher 2022-10-31 /pmc/articles/PMC9691344/ /pubmed/36438498 http://dx.doi.org/10.7150/thno.72853 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Giguelay, Ambre Turtoi, Evgenia Khelaf, Lakhdar Tosato, Guillaume Dadi, Ikrame Chastel, Tommy Poul, Marie-Alix Pratlong, Marine Nicolescu, Stefan Severac, Dany Adenis, Antoine Sgarbura, Olivia Carrère, Sébastien Rouanet, Philippe Quenet, François Ychou, Marc Pourquier, Didier Colombo, Pierre-Emmanuel Turtoi, Andrei Colinge, Jacques The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
title | The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
title_full | The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
title_fullStr | The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
title_full_unstemmed | The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
title_short | The landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
title_sort | landscape of cancer-associated fibroblasts in colorectal cancer liver metastases |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691344/ https://www.ncbi.nlm.nih.gov/pubmed/36438498 http://dx.doi.org/10.7150/thno.72853 |
work_keys_str_mv | AT giguelayambre thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT turtoievgenia thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT khelaflakhdar thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT tosatoguillaume thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT dadiikrame thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT chasteltommy thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT poulmariealix thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT pratlongmarine thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT nicolescustefan thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT severacdany thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT adenisantoine thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT sgarburaolivia thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT carreresebastien thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT rouanetphilippe thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT quenetfrancois thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT ychoumarc thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT pourquierdidier thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT colombopierreemmanuel thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT turtoiandrei thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT colingejacques thelandscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT giguelayambre landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT turtoievgenia landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT khelaflakhdar landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT tosatoguillaume landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT dadiikrame landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT chasteltommy landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT poulmariealix landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT pratlongmarine landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT nicolescustefan landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT severacdany landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT adenisantoine landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT sgarburaolivia landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT carreresebastien landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT rouanetphilippe landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT quenetfrancois landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT ychoumarc landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT pourquierdidier landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT colombopierreemmanuel landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT turtoiandrei landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases AT colingejacques landscapeofcancerassociatedfibroblastsincolorectalcancerlivermetastases |