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Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer
Excess mental stress may harm health, and even accelerate cancer initiation and progression. One fourth of breast cancer patients suffer mental stress including anxiety, sadness, or depression, which negatively affect prognosis and survival. However, the regulatory mechanism is yet to be determined....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542049/ https://www.ncbi.nlm.nih.gov/pubmed/34689156 http://dx.doi.org/10.1038/s41419-021-04280-9 |
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author | Ma, Wenjing Liu, Pengfei Zheng, Jie Lü, Jinhui Zhao, Qian Li, Danni Guo, Yuefan Qian, Lu Wang, Qiong Miao, Xinman Yu, Zuoren |
author_facet | Ma, Wenjing Liu, Pengfei Zheng, Jie Lü, Jinhui Zhao, Qian Li, Danni Guo, Yuefan Qian, Lu Wang, Qiong Miao, Xinman Yu, Zuoren |
author_sort | Ma, Wenjing |
collection | PubMed |
description | Excess mental stress may harm health, and even accelerate cancer initiation and progression. One fourth of breast cancer patients suffer mental stress including anxiety, sadness, or depression, which negatively affect prognosis and survival. However, the regulatory mechanism is yet to be determined. Herein, we applied unpredictable stress stimuli to the breast tumor-bearing mice to establish a xenograft model of breast cancer suffering mental stress, followed by behavioral tests, tumor growth tracking, immune analysis, miRNA screening, and tumor cell proliferation analysis as well. As a result, increased stress hormone levels in serum, decreased percentage of T and NK cells in both blood and tumor samples and accelerated tumor growth in vivo were observed in the mice exposed to mental stress. Promoted cell proliferation was observed in both primary tumor cells derived from the stressed mice and 4T1 breast cancer cells treated with stress hormone corticosterone. In addition, a subset of miRNAs including miR-326, 346, 493, 595, 615, and 665 were identified through a miRNA screening with downregulation in tumors of the stressed mice. CCND1 was identified as a common target gene of miR-346 and miR-493, the top two most significantly downregulated miRNAs by stress exposure. The stress-miRNA-CCND1 signaling regulation of the tumor cell proliferation was further validated in 4T1 cells treated with corticosterone in vitro. GO terms and KEGG pathways analyses on the target genes of miR-346 and miR-493 revealed their involvement in the regulation of human cancer and neuron system, indicating the importance of non-coding genome in mediating the mental stress-induced cancer regulation. In conclusion, this study not only explored immune and nonimmune mechanisms through which mental stress exposure contributes to tumor growth in breast cancer, but also suggested a new therapeutic strategy for cancer patients suffering mental stress. |
format | Online Article Text |
id | pubmed-8542049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85420492021-11-04 Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer Ma, Wenjing Liu, Pengfei Zheng, Jie Lü, Jinhui Zhao, Qian Li, Danni Guo, Yuefan Qian, Lu Wang, Qiong Miao, Xinman Yu, Zuoren Cell Death Dis Article Excess mental stress may harm health, and even accelerate cancer initiation and progression. One fourth of breast cancer patients suffer mental stress including anxiety, sadness, or depression, which negatively affect prognosis and survival. However, the regulatory mechanism is yet to be determined. Herein, we applied unpredictable stress stimuli to the breast tumor-bearing mice to establish a xenograft model of breast cancer suffering mental stress, followed by behavioral tests, tumor growth tracking, immune analysis, miRNA screening, and tumor cell proliferation analysis as well. As a result, increased stress hormone levels in serum, decreased percentage of T and NK cells in both blood and tumor samples and accelerated tumor growth in vivo were observed in the mice exposed to mental stress. Promoted cell proliferation was observed in both primary tumor cells derived from the stressed mice and 4T1 breast cancer cells treated with stress hormone corticosterone. In addition, a subset of miRNAs including miR-326, 346, 493, 595, 615, and 665 were identified through a miRNA screening with downregulation in tumors of the stressed mice. CCND1 was identified as a common target gene of miR-346 and miR-493, the top two most significantly downregulated miRNAs by stress exposure. The stress-miRNA-CCND1 signaling regulation of the tumor cell proliferation was further validated in 4T1 cells treated with corticosterone in vitro. GO terms and KEGG pathways analyses on the target genes of miR-346 and miR-493 revealed their involvement in the regulation of human cancer and neuron system, indicating the importance of non-coding genome in mediating the mental stress-induced cancer regulation. In conclusion, this study not only explored immune and nonimmune mechanisms through which mental stress exposure contributes to tumor growth in breast cancer, but also suggested a new therapeutic strategy for cancer patients suffering mental stress. Nature Publishing Group UK 2021-10-23 /pmc/articles/PMC8542049/ /pubmed/34689156 http://dx.doi.org/10.1038/s41419-021-04280-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ma, Wenjing Liu, Pengfei Zheng, Jie Lü, Jinhui Zhao, Qian Li, Danni Guo, Yuefan Qian, Lu Wang, Qiong Miao, Xinman Yu, Zuoren Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
title | Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
title_full | Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
title_fullStr | Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
title_full_unstemmed | Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
title_short | Immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
title_sort | immune and nonimmune mechanisms mediate the mental stress-induced tumor growth in a xenograft model of breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542049/ https://www.ncbi.nlm.nih.gov/pubmed/34689156 http://dx.doi.org/10.1038/s41419-021-04280-9 |
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