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Chronic stress in solid tumor development: from mechanisms to interventions

Chronic stress results in disturbances of body hormones through the neuroendocrine system. Cancer patients often experience recurrent anxiety and restlessness during disease progression and treatment, which aggravates disease progression and hinders treatment effects. Recent studies have shown that...

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Autores principales: Yan, Jiajing, Chen, Yibing, Luo, Minhua, Hu, Xinyu, Li, Hongsheng, Liu, Quentin, Zou, Zhengzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883141/
https://www.ncbi.nlm.nih.gov/pubmed/36707854
http://dx.doi.org/10.1186/s12929-023-00903-9
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author Yan, Jiajing
Chen, Yibing
Luo, Minhua
Hu, Xinyu
Li, Hongsheng
Liu, Quentin
Zou, Zhengzhi
author_facet Yan, Jiajing
Chen, Yibing
Luo, Minhua
Hu, Xinyu
Li, Hongsheng
Liu, Quentin
Zou, Zhengzhi
author_sort Yan, Jiajing
collection PubMed
description Chronic stress results in disturbances of body hormones through the neuroendocrine system. Cancer patients often experience recurrent anxiety and restlessness during disease progression and treatment, which aggravates disease progression and hinders treatment effects. Recent studies have shown that chronic stress-regulated neuroendocrine systems secret hormones to activate many signaling pathways related to tumor development in tumor cells. The activated neuroendocrine system acts not only on tumor cells but also modulates the survival and metabolic changes of surrounding non-cancerous cells. Current clinical evidences also suggest that chronic stress affects the outcome of cancer treatment. However, in clinic, there is lack of effective treatment for chronic stress in cancer patients. In this review, we discuss the main mechanisms by which chronic stress regulates the tumor microenvironment, including functional regulation of tumor cells by stress hormones (stem cell-like properties, metastasis, angiogenesis, DNA damage accumulation, and apoptotic resistance), metabolic reprogramming and immune escape, and peritumor neuromodulation. Based on the current clinical treatment framework for cancer and chronic stress, we also summarize pharmacological and non-pharmacological therapeutic approaches to provide some directions for cancer therapy.
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spelling pubmed-98831412023-01-29 Chronic stress in solid tumor development: from mechanisms to interventions Yan, Jiajing Chen, Yibing Luo, Minhua Hu, Xinyu Li, Hongsheng Liu, Quentin Zou, Zhengzhi J Biomed Sci Review Chronic stress results in disturbances of body hormones through the neuroendocrine system. Cancer patients often experience recurrent anxiety and restlessness during disease progression and treatment, which aggravates disease progression and hinders treatment effects. Recent studies have shown that chronic stress-regulated neuroendocrine systems secret hormones to activate many signaling pathways related to tumor development in tumor cells. The activated neuroendocrine system acts not only on tumor cells but also modulates the survival and metabolic changes of surrounding non-cancerous cells. Current clinical evidences also suggest that chronic stress affects the outcome of cancer treatment. However, in clinic, there is lack of effective treatment for chronic stress in cancer patients. In this review, we discuss the main mechanisms by which chronic stress regulates the tumor microenvironment, including functional regulation of tumor cells by stress hormones (stem cell-like properties, metastasis, angiogenesis, DNA damage accumulation, and apoptotic resistance), metabolic reprogramming and immune escape, and peritumor neuromodulation. Based on the current clinical treatment framework for cancer and chronic stress, we also summarize pharmacological and non-pharmacological therapeutic approaches to provide some directions for cancer therapy. BioMed Central 2023-01-28 /pmc/articles/PMC9883141/ /pubmed/36707854 http://dx.doi.org/10.1186/s12929-023-00903-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Yan, Jiajing
Chen, Yibing
Luo, Minhua
Hu, Xinyu
Li, Hongsheng
Liu, Quentin
Zou, Zhengzhi
Chronic stress in solid tumor development: from mechanisms to interventions
title Chronic stress in solid tumor development: from mechanisms to interventions
title_full Chronic stress in solid tumor development: from mechanisms to interventions
title_fullStr Chronic stress in solid tumor development: from mechanisms to interventions
title_full_unstemmed Chronic stress in solid tumor development: from mechanisms to interventions
title_short Chronic stress in solid tumor development: from mechanisms to interventions
title_sort chronic stress in solid tumor development: from mechanisms to interventions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883141/
https://www.ncbi.nlm.nih.gov/pubmed/36707854
http://dx.doi.org/10.1186/s12929-023-00903-9
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