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Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling
INTRODUCTION: Breast cancer remains the second leading cause of cancer-related deaths for women in the United States. Metastasis is regulated not only by intrinsic genetic changes in malignant cells, but also by the microenvironment, especially those associated with chronic inflammation. We recently...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672823/ https://www.ncbi.nlm.nih.gov/pubmed/23577751 http://dx.doi.org/10.1186/bcr3412 |
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author | Roy, Lopamudra Das Curry, Jennifer M Sahraei, Mahnaz Besmer, Dahlia M Kidiyoor, Amritha Gruber, Helen E Mukherjee, Pinku |
author_facet | Roy, Lopamudra Das Curry, Jennifer M Sahraei, Mahnaz Besmer, Dahlia M Kidiyoor, Amritha Gruber, Helen E Mukherjee, Pinku |
author_sort | Roy, Lopamudra Das |
collection | PubMed |
description | INTRODUCTION: Breast cancer remains the second leading cause of cancer-related deaths for women in the United States. Metastasis is regulated not only by intrinsic genetic changes in malignant cells, but also by the microenvironment, especially those associated with chronic inflammation. We recently reported that mice with autoimmune arthritis have significantly increased incidence of bone and lung metastasis and decreased survival associated with breast cancer. In this study, we evaluated the mechanism underlying the increased metastasis. METHODS: We used two mouse models; one that develops spontaneous autoimmune arthritis (SKG mice) injected with metastatic breast cancer cells (4T1), and another that develops spontaneous breast cancer (MMTV-PyV MT mice) injected with type II collagen to induce autoimmune arthritis. Mast cell levels and metastasis were monitored. RESULTS: First, we confirmed that breast tumor-bearing arthritic mice have a significantly higher incidence of bone and lung metastasis than do their nonarthritic counterparts. Next, we showed increased recruitment of mast cells within the primary tumor of arthritic mice, which facilitates metastasis. Next, we report that arthritic mice without any tumors have higher numbers of mast cells in the bones and lungs, which may be the underlying cause for the enhanced lung and bone metastases observed in the arthritic mice. Next, we showed that once the tumor cells populate the metastatic niches (bones and lungs), they further increase the mast cell population within the niche and assist in enhancing metastasis. This may primarily be due to the interaction of c-Kit receptor present on mast cells and stem cell factor (SCF, the ligand for ckit) expressed on tumor cells. Finally, we showed that targeting the SCF/cKit interaction with an anti-ckit antibody reduces the differentiation of mast cells and consequently reduces metastasis. CONCLUSION: This is the first report to show that mast cells may play a critical role in remodeling not only the tumor microenvironment but also the metastatic niche to facilitate efficient metastasis through SCF/cKit interaction in breast cancer with arthritis. |
format | Online Article Text |
id | pubmed-3672823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36728232013-06-06 Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling Roy, Lopamudra Das Curry, Jennifer M Sahraei, Mahnaz Besmer, Dahlia M Kidiyoor, Amritha Gruber, Helen E Mukherjee, Pinku Breast Cancer Res Research Article INTRODUCTION: Breast cancer remains the second leading cause of cancer-related deaths for women in the United States. Metastasis is regulated not only by intrinsic genetic changes in malignant cells, but also by the microenvironment, especially those associated with chronic inflammation. We recently reported that mice with autoimmune arthritis have significantly increased incidence of bone and lung metastasis and decreased survival associated with breast cancer. In this study, we evaluated the mechanism underlying the increased metastasis. METHODS: We used two mouse models; one that develops spontaneous autoimmune arthritis (SKG mice) injected with metastatic breast cancer cells (4T1), and another that develops spontaneous breast cancer (MMTV-PyV MT mice) injected with type II collagen to induce autoimmune arthritis. Mast cell levels and metastasis were monitored. RESULTS: First, we confirmed that breast tumor-bearing arthritic mice have a significantly higher incidence of bone and lung metastasis than do their nonarthritic counterparts. Next, we showed increased recruitment of mast cells within the primary tumor of arthritic mice, which facilitates metastasis. Next, we report that arthritic mice without any tumors have higher numbers of mast cells in the bones and lungs, which may be the underlying cause for the enhanced lung and bone metastases observed in the arthritic mice. Next, we showed that once the tumor cells populate the metastatic niches (bones and lungs), they further increase the mast cell population within the niche and assist in enhancing metastasis. This may primarily be due to the interaction of c-Kit receptor present on mast cells and stem cell factor (SCF, the ligand for ckit) expressed on tumor cells. Finally, we showed that targeting the SCF/cKit interaction with an anti-ckit antibody reduces the differentiation of mast cells and consequently reduces metastasis. CONCLUSION: This is the first report to show that mast cells may play a critical role in remodeling not only the tumor microenvironment but also the metastatic niche to facilitate efficient metastasis through SCF/cKit interaction in breast cancer with arthritis. BioMed Central 2013 2013-04-11 /pmc/articles/PMC3672823/ /pubmed/23577751 http://dx.doi.org/10.1186/bcr3412 Text en Copyright © 2013 Roy 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 cited. |
spellingShingle | Research Article Roy, Lopamudra Das Curry, Jennifer M Sahraei, Mahnaz Besmer, Dahlia M Kidiyoor, Amritha Gruber, Helen E Mukherjee, Pinku Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling |
title | Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling |
title_full | Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling |
title_fullStr | Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling |
title_full_unstemmed | Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling |
title_short | Arthritis augments breast cancer metastasis: role of mast cells and SCF/c-Kit signaling |
title_sort | arthritis augments breast cancer metastasis: role of mast cells and scf/c-kit signaling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672823/ https://www.ncbi.nlm.nih.gov/pubmed/23577751 http://dx.doi.org/10.1186/bcr3412 |
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