Cargando…

The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells

Hepatic stellate cells (HSC) play a major role in initiating the liver fibrogenic (wounding) response of the liver and can also orchestrate a pro-metastatic microenvironment in the liver in response to invading cancer cells. Here we explored the role of the hepatic stellate cells in colon carcinoma...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernandez, Maria Celia, Rayes, Roni, Ham, Boram, Wang, Ni, Bourdeau, France, Milette, Simon, lllemann, Martin, Bird, Nigel, Majeed, Ali, Xu, Jun, Kisselova, Tatiana, Brodt, Pnina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581028/
https://www.ncbi.nlm.nih.gov/pubmed/28881729
http://dx.doi.org/10.18632/oncotarget.12595
_version_ 1783260982004416512
author Fernandez, Maria Celia
Rayes, Roni
Ham, Boram
Wang, Ni
Bourdeau, France
Milette, Simon
lllemann, Martin
Bird, Nigel
Majeed, Ali
Xu, Jun
Kisselova, Tatiana
Brodt, Pnina
author_facet Fernandez, Maria Celia
Rayes, Roni
Ham, Boram
Wang, Ni
Bourdeau, France
Milette, Simon
lllemann, Martin
Bird, Nigel
Majeed, Ali
Xu, Jun
Kisselova, Tatiana
Brodt, Pnina
author_sort Fernandez, Maria Celia
collection PubMed
description Hepatic stellate cells (HSC) play a major role in initiating the liver fibrogenic (wounding) response of the liver and can also orchestrate a pro-metastatic microenvironment in the liver in response to invading cancer cells. Here we explored the role of the hepatic stellate cells in colon carcinoma liver metastasis with emphasis on the contribution of the insulin-like growth factor (IGF) axis to their activation and function. To this end, we used mice with a Tamoxifen inducible liver IGF-I deficiency. We found that in mice with a sustained IGF-I deficiency, recruitment and activation of HSC into tumor-infiltrated areas of the liver were markedly diminished, resulting in decreased collagen deposition and reduced tumor expansion. In addition, IGF-I could rescue HSC from apoptosis induced by pro-inflammatory factors such as TNF-α known to be upregulated in the early stages of liver metastasis. Moreover, in surgical specimens, activated IGF-IR was observed on HSC-like stromal cells surrounding colorectal carcinoma liver metastases. Finally, IGF-targeting in vivo using an IGF-Trap caused a significant reduction in HSC activation in response to metastatic colon cancer cells. Therefore, our data identify IGF as a survival factor for HSC and thereby, a promoter of the pro-metastatic microenvironment in the liver. IGF-targeting could therefore provide a strategy for curtailing the pro-metastatic host response of the liver during the early stages of liver metastasis.
format Online
Article
Text
id pubmed-5581028
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-55810282017-09-06 The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells Fernandez, Maria Celia Rayes, Roni Ham, Boram Wang, Ni Bourdeau, France Milette, Simon lllemann, Martin Bird, Nigel Majeed, Ali Xu, Jun Kisselova, Tatiana Brodt, Pnina Oncotarget Research Paper Hepatic stellate cells (HSC) play a major role in initiating the liver fibrogenic (wounding) response of the liver and can also orchestrate a pro-metastatic microenvironment in the liver in response to invading cancer cells. Here we explored the role of the hepatic stellate cells in colon carcinoma liver metastasis with emphasis on the contribution of the insulin-like growth factor (IGF) axis to their activation and function. To this end, we used mice with a Tamoxifen inducible liver IGF-I deficiency. We found that in mice with a sustained IGF-I deficiency, recruitment and activation of HSC into tumor-infiltrated areas of the liver were markedly diminished, resulting in decreased collagen deposition and reduced tumor expansion. In addition, IGF-I could rescue HSC from apoptosis induced by pro-inflammatory factors such as TNF-α known to be upregulated in the early stages of liver metastasis. Moreover, in surgical specimens, activated IGF-IR was observed on HSC-like stromal cells surrounding colorectal carcinoma liver metastases. Finally, IGF-targeting in vivo using an IGF-Trap caused a significant reduction in HSC activation in response to metastatic colon cancer cells. Therefore, our data identify IGF as a survival factor for HSC and thereby, a promoter of the pro-metastatic microenvironment in the liver. IGF-targeting could therefore provide a strategy for curtailing the pro-metastatic host response of the liver during the early stages of liver metastasis. Impact Journals LLC 2016-10-12 /pmc/articles/PMC5581028/ /pubmed/28881729 http://dx.doi.org/10.18632/oncotarget.12595 Text en Copyright: © 2017 Fernandez et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Fernandez, Maria Celia
Rayes, Roni
Ham, Boram
Wang, Ni
Bourdeau, France
Milette, Simon
lllemann, Martin
Bird, Nigel
Majeed, Ali
Xu, Jun
Kisselova, Tatiana
Brodt, Pnina
The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
title The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
title_full The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
title_fullStr The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
title_full_unstemmed The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
title_short The type I insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
title_sort type i insulin-like growth factor regulates the liver stromal response to metastatic colon carcinoma cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581028/
https://www.ncbi.nlm.nih.gov/pubmed/28881729
http://dx.doi.org/10.18632/oncotarget.12595
work_keys_str_mv AT fernandezmariacelia thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT rayesroni thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT hamboram thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT wangni thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT bourdeaufrance thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT milettesimon thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT lllemannmartin thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT birdnigel thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT majeedali thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT xujun thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT kisselovatatiana thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT brodtpnina thetypeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT fernandezmariacelia typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT rayesroni typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT hamboram typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT wangni typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT bourdeaufrance typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT milettesimon typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT lllemannmartin typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT birdnigel typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT majeedali typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT xujun typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT kisselovatatiana typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells
AT brodtpnina typeiinsulinlikegrowthfactorregulatestheliverstromalresponsetometastaticcoloncarcinomacells