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Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies

SIMPLE SUMMARY: In this review, we present knowledge of the molecular mechanisms and therapeutic strategies of bone metastasis of breast cancer, particularly the interaction between metastatic breast cancer cells and the bone microenvironment in promoting the development of bone metastasis in breast...

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Autores principales: Pang, Lulian, Gan, Chen, Xu, Jian, Jia, Yingxue, Chai, Jiaying, Huang, Runze, Li, Anlong, Ge, Han, Yu, Sheng, Cheng, Huaidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738274/
https://www.ncbi.nlm.nih.gov/pubmed/36497209
http://dx.doi.org/10.3390/cancers14235727
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author Pang, Lulian
Gan, Chen
Xu, Jian
Jia, Yingxue
Chai, Jiaying
Huang, Runze
Li, Anlong
Ge, Han
Yu, Sheng
Cheng, Huaidong
author_facet Pang, Lulian
Gan, Chen
Xu, Jian
Jia, Yingxue
Chai, Jiaying
Huang, Runze
Li, Anlong
Ge, Han
Yu, Sheng
Cheng, Huaidong
author_sort Pang, Lulian
collection PubMed
description SIMPLE SUMMARY: In this review, we present knowledge of the molecular mechanisms and therapeutic strategies of bone metastasis of breast cancer, particularly the interaction between metastatic breast cancer cells and the bone microenvironment in promoting the development of bone metastasis in breast cancer patients, with the aim of improving the quality of life and prognosis of breast cancer patients and providing a reference for future research directions. ABSTRACT: Bone metastasis is a common complication of many types of advanced cancer, including breast cancer. Bone metastasis may cause severe pain, fractures, and hypercalcemia, rendering clinical management challenging and substantially reducing the quality of life and overall survival (OS) time of breast cancer patients. Studies have revealed that bone metastasis is related to interactions between tumor cells and the bone microenvironment, and involves complex molecular biological mechanisms, including colonization, osteolytic destruction, and an immunosuppressive bone microenvironment. Agents inhibiting bone metastasis (such as bisphosphate and denosumab) alleviate bone destruction and improve the quality of life of breast cancer patients with bone metastasis. However, the prognosis of these patients remains poor, and the specific biological mechanism of bone metastasis is incompletely understood. Additional basic and clinical studies are urgently needed, to further explore the mechanism of bone metastasis and develop new therapeutic drugs. This review presents a summary of the molecular mechanisms and therapeutic strategies of bone metastasis of breast cancer, aiming to improve the quality of life and prognosis of breast cancer patients and provide a reference for future research directions.
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spelling pubmed-97382742022-12-11 Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies Pang, Lulian Gan, Chen Xu, Jian Jia, Yingxue Chai, Jiaying Huang, Runze Li, Anlong Ge, Han Yu, Sheng Cheng, Huaidong Cancers (Basel) Review SIMPLE SUMMARY: In this review, we present knowledge of the molecular mechanisms and therapeutic strategies of bone metastasis of breast cancer, particularly the interaction between metastatic breast cancer cells and the bone microenvironment in promoting the development of bone metastasis in breast cancer patients, with the aim of improving the quality of life and prognosis of breast cancer patients and providing a reference for future research directions. ABSTRACT: Bone metastasis is a common complication of many types of advanced cancer, including breast cancer. Bone metastasis may cause severe pain, fractures, and hypercalcemia, rendering clinical management challenging and substantially reducing the quality of life and overall survival (OS) time of breast cancer patients. Studies have revealed that bone metastasis is related to interactions between tumor cells and the bone microenvironment, and involves complex molecular biological mechanisms, including colonization, osteolytic destruction, and an immunosuppressive bone microenvironment. Agents inhibiting bone metastasis (such as bisphosphate and denosumab) alleviate bone destruction and improve the quality of life of breast cancer patients with bone metastasis. However, the prognosis of these patients remains poor, and the specific biological mechanism of bone metastasis is incompletely understood. Additional basic and clinical studies are urgently needed, to further explore the mechanism of bone metastasis and develop new therapeutic drugs. This review presents a summary of the molecular mechanisms and therapeutic strategies of bone metastasis of breast cancer, aiming to improve the quality of life and prognosis of breast cancer patients and provide a reference for future research directions. MDPI 2022-11-22 /pmc/articles/PMC9738274/ /pubmed/36497209 http://dx.doi.org/10.3390/cancers14235727 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pang, Lulian
Gan, Chen
Xu, Jian
Jia, Yingxue
Chai, Jiaying
Huang, Runze
Li, Anlong
Ge, Han
Yu, Sheng
Cheng, Huaidong
Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies
title Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies
title_full Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies
title_fullStr Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies
title_full_unstemmed Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies
title_short Bone Metastasis of Breast Cancer: Molecular Mechanisms and Therapeutic Strategies
title_sort bone metastasis of breast cancer: molecular mechanisms and therapeutic strategies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738274/
https://www.ncbi.nlm.nih.gov/pubmed/36497209
http://dx.doi.org/10.3390/cancers14235727
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