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Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy

HMGB1 is a member of highly conserved high mobility group protein superfamily with intracellular and extracellular distribution. Abnormal HMGB1 levels are frequently manifested in various malignant diseases, including breast cancer. Numerous studies have revealed the clinical value of HMGB1 in the d...

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Detalles Bibliográficos
Autores principales: Dong, Haonan, Zhang, Lu, Liu, Suling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134916/
https://www.ncbi.nlm.nih.gov/pubmed/35637945
http://dx.doi.org/10.7150/ijbs.73504
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author Dong, Haonan
Zhang, Lu
Liu, Suling
author_facet Dong, Haonan
Zhang, Lu
Liu, Suling
author_sort Dong, Haonan
collection PubMed
description HMGB1 is a member of highly conserved high mobility group protein superfamily with intracellular and extracellular distribution. Abnormal HMGB1 levels are frequently manifested in various malignant diseases, including breast cancer. Numerous studies have revealed the clinical value of HMGB1 in the diagnosis and therapy of breast cancer. However, the dual function of pro- and anti-tumor makes HMGB1 in cancer progression requires more profound understanding. This review summarizes the functions and mechanisms of HMGB1 on regulating breast cancer, including autophagy, immunogenic cell death, and interaction with the tumor microenvironment. These functions determine the strategies for the development of chemotherapy, radiotherapy, immunotherapy and combination therapies by targeting HMGB1 in breast cancer. Defining the mechanisms of HMGB1 on regulating breast cancer development and progression will facilitate the application of HMGB1 as a therapeutic target for breast cancer.
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spelling pubmed-91349162022-05-29 Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy Dong, Haonan Zhang, Lu Liu, Suling Int J Biol Sci Review HMGB1 is a member of highly conserved high mobility group protein superfamily with intracellular and extracellular distribution. Abnormal HMGB1 levels are frequently manifested in various malignant diseases, including breast cancer. Numerous studies have revealed the clinical value of HMGB1 in the diagnosis and therapy of breast cancer. However, the dual function of pro- and anti-tumor makes HMGB1 in cancer progression requires more profound understanding. This review summarizes the functions and mechanisms of HMGB1 on regulating breast cancer, including autophagy, immunogenic cell death, and interaction with the tumor microenvironment. These functions determine the strategies for the development of chemotherapy, radiotherapy, immunotherapy and combination therapies by targeting HMGB1 in breast cancer. Defining the mechanisms of HMGB1 on regulating breast cancer development and progression will facilitate the application of HMGB1 as a therapeutic target for breast cancer. Ivyspring International Publisher 2022-05-09 /pmc/articles/PMC9134916/ /pubmed/35637945 http://dx.doi.org/10.7150/ijbs.73504 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Dong, Haonan
Zhang, Lu
Liu, Suling
Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy
title Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy
title_full Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy
title_fullStr Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy
title_full_unstemmed Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy
title_short Targeting HMGB1: An available Therapeutic Strategy for Breast Cancer Therapy
title_sort targeting hmgb1: an available therapeutic strategy for breast cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134916/
https://www.ncbi.nlm.nih.gov/pubmed/35637945
http://dx.doi.org/10.7150/ijbs.73504
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