Cargando…
Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR
Matrix metalloproteinase 11 (MMP11) is an extracellular proteolytic enzyme belonging to the matrix metalloproteinase (MMP11) family. These proteases are involved in extracellular matrix (ECM) remodeling and activation of latent factors. MMP11 is a negative regulator of adipose tissue development and...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565046/ https://www.ncbi.nlm.nih.gov/pubmed/32825455 http://dx.doi.org/10.3390/cancers12092357 |
_version_ | 1783595851578343424 |
---|---|
author | Tan, Bing Jaulin, Amélie Bund, Caroline Outilaft, Hassiba Wendling, Corinne Chenard, Marie-Pierrette Alpy, Fabien Cicek, A. Ercüment Namer, Izzie J. Tomasetto, Catherine Dali-Youcef, Nassim |
author_facet | Tan, Bing Jaulin, Amélie Bund, Caroline Outilaft, Hassiba Wendling, Corinne Chenard, Marie-Pierrette Alpy, Fabien Cicek, A. Ercüment Namer, Izzie J. Tomasetto, Catherine Dali-Youcef, Nassim |
author_sort | Tan, Bing |
collection | PubMed |
description | Matrix metalloproteinase 11 (MMP11) is an extracellular proteolytic enzyme belonging to the matrix metalloproteinase (MMP11) family. These proteases are involved in extracellular matrix (ECM) remodeling and activation of latent factors. MMP11 is a negative regulator of adipose tissue development and controls energy metabolism in vivo. In cancer, MMP11 expression is associated with poorer survival, and preclinical studies in mice showed that MMP11 accelerates tumor growth. How the metabolic role of MMP11 contributes to cancer development is poorly understood. To address this issue, we developed a series of preclinical mouse mammary gland tumor models by genetic engineering. Tumor growth was studied in mice either deficient (Loss of Function-LOF) or overexpressing MMP11 (Gain of Function-GOF) crossed with a transgenic model of breast cancer induced by the polyoma middle T antigen (PyMT) driven by the murine mammary tumor virus promoter (MMTV) (MMTV-PyMT). Both GOF and LOF models support roles for MMP11, favoring early tumor growth by increasing proliferation and reducing apoptosis. Of interest, MMP11 promotes Insulin-like Growth Factor-1 (IGF1)/protein kinase B (AKT)/Forkhead box protein O1 (FoxO1) signaling and is associated with a metabolic switch in the tumor, activation of the endoplasmic reticulum stress response, and an alteration in the mitochondrial unfolded protein response with decreased proteasome activity. In addition, high resonance magic angle spinning (HRMAS) metabolomics analysis of tumors from both models established a metabolic signature that favors tumorigenesis when MMP11 is overexpressed. These data support the idea that MMP11 contributes to an adaptive metabolic response, named metabolic flexibility, promoting cancer growth. |
format | Online Article Text |
id | pubmed-7565046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75650462020-10-26 Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR Tan, Bing Jaulin, Amélie Bund, Caroline Outilaft, Hassiba Wendling, Corinne Chenard, Marie-Pierrette Alpy, Fabien Cicek, A. Ercüment Namer, Izzie J. Tomasetto, Catherine Dali-Youcef, Nassim Cancers (Basel) Article Matrix metalloproteinase 11 (MMP11) is an extracellular proteolytic enzyme belonging to the matrix metalloproteinase (MMP11) family. These proteases are involved in extracellular matrix (ECM) remodeling and activation of latent factors. MMP11 is a negative regulator of adipose tissue development and controls energy metabolism in vivo. In cancer, MMP11 expression is associated with poorer survival, and preclinical studies in mice showed that MMP11 accelerates tumor growth. How the metabolic role of MMP11 contributes to cancer development is poorly understood. To address this issue, we developed a series of preclinical mouse mammary gland tumor models by genetic engineering. Tumor growth was studied in mice either deficient (Loss of Function-LOF) or overexpressing MMP11 (Gain of Function-GOF) crossed with a transgenic model of breast cancer induced by the polyoma middle T antigen (PyMT) driven by the murine mammary tumor virus promoter (MMTV) (MMTV-PyMT). Both GOF and LOF models support roles for MMP11, favoring early tumor growth by increasing proliferation and reducing apoptosis. Of interest, MMP11 promotes Insulin-like Growth Factor-1 (IGF1)/protein kinase B (AKT)/Forkhead box protein O1 (FoxO1) signaling and is associated with a metabolic switch in the tumor, activation of the endoplasmic reticulum stress response, and an alteration in the mitochondrial unfolded protein response with decreased proteasome activity. In addition, high resonance magic angle spinning (HRMAS) metabolomics analysis of tumors from both models established a metabolic signature that favors tumorigenesis when MMP11 is overexpressed. These data support the idea that MMP11 contributes to an adaptive metabolic response, named metabolic flexibility, promoting cancer growth. MDPI 2020-08-20 /pmc/articles/PMC7565046/ /pubmed/32825455 http://dx.doi.org/10.3390/cancers12092357 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 Tan, Bing Jaulin, Amélie Bund, Caroline Outilaft, Hassiba Wendling, Corinne Chenard, Marie-Pierrette Alpy, Fabien Cicek, A. Ercüment Namer, Izzie J. Tomasetto, Catherine Dali-Youcef, Nassim Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR |
title | Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR |
title_full | Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR |
title_fullStr | Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR |
title_full_unstemmed | Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR |
title_short | Matrix Metalloproteinase-11 Promotes Early Mouse Mammary Gland Tumor Growth through Metabolic Reprogramming and Increased IGF1/AKT/FoxO1 Signaling Pathway, Enhanced ER Stress and Alteration in Mitochondrial UPR |
title_sort | matrix metalloproteinase-11 promotes early mouse mammary gland tumor growth through metabolic reprogramming and increased igf1/akt/foxo1 signaling pathway, enhanced er stress and alteration in mitochondrial upr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565046/ https://www.ncbi.nlm.nih.gov/pubmed/32825455 http://dx.doi.org/10.3390/cancers12092357 |
work_keys_str_mv | AT tanbing matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT jaulinamelie matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT bundcaroline matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT outilafthassiba matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT wendlingcorinne matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT chenardmariepierrette matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT alpyfabien matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT cicekaercument matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT namerizziej matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT tomasettocatherine matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr AT daliyoucefnassim matrixmetalloproteinase11promotesearlymousemammaryglandtumorgrowththroughmetabolicreprogrammingandincreasedigf1aktfoxo1signalingpathwayenhancederstressandalterationinmitochondrialupr |