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Cancer-associated adipocytes: emerging supporters in breast cancer
Breast cancer (BC) is a malignant breast tumor confronted with high invasion, metastasis and recurrence rate, and adipocytes are the largest components in breast tissue. The aberrant adipocytes, especially the BC-neighbored cancer-associated adipocytes (CAAs), are found in the invasive front of BC....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425140/ https://www.ncbi.nlm.nih.gov/pubmed/32787888 http://dx.doi.org/10.1186/s13046-020-01666-z |
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author | Zhao, Chongru Wu, Min Zeng, Ning Xiong, Mingchen Hu, Weijie Lv, Wenchang Yi, Yi Zhang, Qi Wu, Yiping |
author_facet | Zhao, Chongru Wu, Min Zeng, Ning Xiong, Mingchen Hu, Weijie Lv, Wenchang Yi, Yi Zhang, Qi Wu, Yiping |
author_sort | Zhao, Chongru |
collection | PubMed |
description | Breast cancer (BC) is a malignant breast tumor confronted with high invasion, metastasis and recurrence rate, and adipocytes are the largest components in breast tissue. The aberrant adipocytes, especially the BC-neighbored cancer-associated adipocytes (CAAs), are found in the invasive front of BC. CAAs present a vicious phenotype compared with mature mammary adipocytes and mediate the crosstalk network between adipocytes and BC cells. By releasing multiple adipokines such as leptin, adiponectin, interleukin (IL)-6, chemokine ligand 2 (CCL2) and chemokine ligand 5 (CCL5), CAAs play essential roles in favor of proliferation, angiogenesis, dissemination, invasion and metastasis of BC. This article reviews the recent existing CAAs studies on the functions and mechanisms of adipocytes in the development of BC, including adipokine regulating, metabolic reprogramming, extracellular matrix (ECM) remodeling, microRNAs (miRNAs) and immune cell adjusting. Besides, adipocyte secretome and cellular interactions are implicated in the intervention to BC therapy and autologous fat grafting of breast reconstruction. Therefore, the potential functions and mechanisms of CAAs are very important for unveiling BC oncogenesis and progress. Deciphering the complex network between CAAs and BC is critical for designing therapeutic strategies and achieving the maximum therapeutic effects of BC. |
format | Online Article Text |
id | pubmed-7425140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74251402020-08-16 Cancer-associated adipocytes: emerging supporters in breast cancer Zhao, Chongru Wu, Min Zeng, Ning Xiong, Mingchen Hu, Weijie Lv, Wenchang Yi, Yi Zhang, Qi Wu, Yiping J Exp Clin Cancer Res Review Breast cancer (BC) is a malignant breast tumor confronted with high invasion, metastasis and recurrence rate, and adipocytes are the largest components in breast tissue. The aberrant adipocytes, especially the BC-neighbored cancer-associated adipocytes (CAAs), are found in the invasive front of BC. CAAs present a vicious phenotype compared with mature mammary adipocytes and mediate the crosstalk network between adipocytes and BC cells. By releasing multiple adipokines such as leptin, adiponectin, interleukin (IL)-6, chemokine ligand 2 (CCL2) and chemokine ligand 5 (CCL5), CAAs play essential roles in favor of proliferation, angiogenesis, dissemination, invasion and metastasis of BC. This article reviews the recent existing CAAs studies on the functions and mechanisms of adipocytes in the development of BC, including adipokine regulating, metabolic reprogramming, extracellular matrix (ECM) remodeling, microRNAs (miRNAs) and immune cell adjusting. Besides, adipocyte secretome and cellular interactions are implicated in the intervention to BC therapy and autologous fat grafting of breast reconstruction. Therefore, the potential functions and mechanisms of CAAs are very important for unveiling BC oncogenesis and progress. Deciphering the complex network between CAAs and BC is critical for designing therapeutic strategies and achieving the maximum therapeutic effects of BC. BioMed Central 2020-08-12 /pmc/articles/PMC7425140/ /pubmed/32787888 http://dx.doi.org/10.1186/s13046-020-01666-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Zhao, Chongru Wu, Min Zeng, Ning Xiong, Mingchen Hu, Weijie Lv, Wenchang Yi, Yi Zhang, Qi Wu, Yiping Cancer-associated adipocytes: emerging supporters in breast cancer |
title | Cancer-associated adipocytes: emerging supporters in breast cancer |
title_full | Cancer-associated adipocytes: emerging supporters in breast cancer |
title_fullStr | Cancer-associated adipocytes: emerging supporters in breast cancer |
title_full_unstemmed | Cancer-associated adipocytes: emerging supporters in breast cancer |
title_short | Cancer-associated adipocytes: emerging supporters in breast cancer |
title_sort | cancer-associated adipocytes: emerging supporters in breast cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425140/ https://www.ncbi.nlm.nih.gov/pubmed/32787888 http://dx.doi.org/10.1186/s13046-020-01666-z |
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