Cargando…
The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro
Cancer associated fibroblasts (CAFs) are central elements of the microenvironment that control tumor development. In breast cancer, CAFs can originate from adipose progenitors (APs). We, and others, have shown that the primary cilium, an antenna-shaped organelle, controls several aspects of APs’ bio...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601294/ https://www.ncbi.nlm.nih.gov/pubmed/33049976 http://dx.doi.org/10.3390/cells9102251 |
_version_ | 1783603376991240192 |
---|---|
author | Peraldi, Pascal Ladoux, Annie Giorgetti-Peraldi, Sophie Dani, Christian |
author_facet | Peraldi, Pascal Ladoux, Annie Giorgetti-Peraldi, Sophie Dani, Christian |
author_sort | Peraldi, Pascal |
collection | PubMed |
description | Cancer associated fibroblasts (CAFs) are central elements of the microenvironment that control tumor development. In breast cancer, CAFs can originate from adipose progenitors (APs). We, and others, have shown that the primary cilium, an antenna-shaped organelle, controls several aspects of APs’ biology. We studied the conversion of human APs into CAFs by breast cancer cell lines (BCCs). Deletion of the cilium of APs by a pharmacological inhibitor, or by siRNA, allow us to demonstrate that the cilium is necessary for the differentiation of APs into CAFs. BCCs increase production of TGF-β1 by APs, which is a known inducer of CAFs. Pharmacological inhibition of TGF-β1 signaling in APs prevents their conversion into CAFs. Since we previously showed that deletion of the APs’ cilium inhibits TGF-β1 signaling, we propose that BCCs induce TGF-β1 production in Aps, which binds to the primary cilium of Aps and leads to their differentiation into CAFs. Inhibition of APs conversion into CAFs induces a loss in some of the biological effects of CAFs since deletion of the cilium of APs decreases their effect on the migration of BCCs. This is the first observation of a function of the cilium of APs in their conversion into CAFs, and its consequences on BCCs. |
format | Online Article Text |
id | pubmed-7601294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76012942020-11-01 The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro Peraldi, Pascal Ladoux, Annie Giorgetti-Peraldi, Sophie Dani, Christian Cells Article Cancer associated fibroblasts (CAFs) are central elements of the microenvironment that control tumor development. In breast cancer, CAFs can originate from adipose progenitors (APs). We, and others, have shown that the primary cilium, an antenna-shaped organelle, controls several aspects of APs’ biology. We studied the conversion of human APs into CAFs by breast cancer cell lines (BCCs). Deletion of the cilium of APs by a pharmacological inhibitor, or by siRNA, allow us to demonstrate that the cilium is necessary for the differentiation of APs into CAFs. BCCs increase production of TGF-β1 by APs, which is a known inducer of CAFs. Pharmacological inhibition of TGF-β1 signaling in APs prevents their conversion into CAFs. Since we previously showed that deletion of the APs’ cilium inhibits TGF-β1 signaling, we propose that BCCs induce TGF-β1 production in Aps, which binds to the primary cilium of Aps and leads to their differentiation into CAFs. Inhibition of APs conversion into CAFs induces a loss in some of the biological effects of CAFs since deletion of the cilium of APs decreases their effect on the migration of BCCs. This is the first observation of a function of the cilium of APs in their conversion into CAFs, and its consequences on BCCs. MDPI 2020-10-08 /pmc/articles/PMC7601294/ /pubmed/33049976 http://dx.doi.org/10.3390/cells9102251 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Peraldi, Pascal Ladoux, Annie Giorgetti-Peraldi, Sophie Dani, Christian The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro |
title | The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro |
title_full | The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro |
title_fullStr | The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro |
title_full_unstemmed | The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro |
title_short | The Primary Cilium of Adipose Progenitors Is Necessary for Their Differentiation into Cancer-Associated Fibroblasts that Promote Migration of Breast Cancer Cells In Vitro |
title_sort | primary cilium of adipose progenitors is necessary for their differentiation into cancer-associated fibroblasts that promote migration of breast cancer cells in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601294/ https://www.ncbi.nlm.nih.gov/pubmed/33049976 http://dx.doi.org/10.3390/cells9102251 |
work_keys_str_mv | AT peraldipascal theprimaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT ladouxannie theprimaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT giorgettiperaldisophie theprimaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT danichristian theprimaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT peraldipascal primaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT ladouxannie primaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT giorgettiperaldisophie primaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro AT danichristian primaryciliumofadiposeprogenitorsisnecessaryfortheirdifferentiationintocancerassociatedfibroblaststhatpromotemigrationofbreastcancercellsinvitro |