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Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells

BACKGROUND: An increasing number of studies indicate that adrenergic signaling plays a fundamental role in tumor progression and metastasis induced by chronic stress. However, despite the growing attention, an understanding of the mechanisms linking chronic stress and cancer is still insufficient. M...

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Autores principales: Zhu, Zhen, Yu, Ruihua, Yang, Chao, Li, Dong, Wang, Jiawei, Yang, Wanli, Ji, Yonghua, Wang, Li, Wang, Yaosheng, Jiang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867925/
https://www.ncbi.nlm.nih.gov/pubmed/33569451
http://dx.doi.org/10.21037/atm-20-8176
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author Zhu, Zhen
Yu, Ruihua
Yang, Chao
Li, Dong
Wang, Jiawei
Yang, Wanli
Ji, Yonghua
Wang, Li
Wang, Yaosheng
Jiang, Feng
author_facet Zhu, Zhen
Yu, Ruihua
Yang, Chao
Li, Dong
Wang, Jiawei
Yang, Wanli
Ji, Yonghua
Wang, Li
Wang, Yaosheng
Jiang, Feng
author_sort Zhu, Zhen
collection PubMed
description BACKGROUND: An increasing number of studies indicate that adrenergic signaling plays a fundamental role in tumor progression and metastasis induced by chronic stress. However, despite the growing attention, an understanding of the mechanisms linking chronic stress and cancer is still insufficient. METHODS: Western blot analysis and transmission electron microscopy (TEM) were used to observe the changes in autophagy level in a breast cancer cell line (MCF-7) after epinephrine treatment. Non-targeted metabolomics was also used to detect MCF-7 metabolites after epinephrine treatment. The xenograft model was used to detect the level of autophagy after epinephrine intervention. RESULTS: The results showed that epinephrine treatment reduced the autophagy level of breast cancer cells. Epinephrine changed the level of phosphatidylethanolamine (PE) in breast cancer cells as detected by non-targeted metabolomics. Epinephrine also changed autophagy in breast cancer cells by decreasing the level of PE in cells. When autophagy decreased, the invasion and migration of breast cancer cells increased in vitro, and the progression of breast cancer accelerated in vivo. CONCLUSIONS: These findings suggest that stress-related hormones affect the tumor progression of breast cancer. Therefore, strengthening the emotional management strategies of patients during the process of antitumor treatment as a supplement to the existing treatments may be beneficial.
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spelling pubmed-78679252021-02-09 Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells Zhu, Zhen Yu, Ruihua Yang, Chao Li, Dong Wang, Jiawei Yang, Wanli Ji, Yonghua Wang, Li Wang, Yaosheng Jiang, Feng Ann Transl Med Original Article BACKGROUND: An increasing number of studies indicate that adrenergic signaling plays a fundamental role in tumor progression and metastasis induced by chronic stress. However, despite the growing attention, an understanding of the mechanisms linking chronic stress and cancer is still insufficient. METHODS: Western blot analysis and transmission electron microscopy (TEM) were used to observe the changes in autophagy level in a breast cancer cell line (MCF-7) after epinephrine treatment. Non-targeted metabolomics was also used to detect MCF-7 metabolites after epinephrine treatment. The xenograft model was used to detect the level of autophagy after epinephrine intervention. RESULTS: The results showed that epinephrine treatment reduced the autophagy level of breast cancer cells. Epinephrine changed the level of phosphatidylethanolamine (PE) in breast cancer cells as detected by non-targeted metabolomics. Epinephrine also changed autophagy in breast cancer cells by decreasing the level of PE in cells. When autophagy decreased, the invasion and migration of breast cancer cells increased in vitro, and the progression of breast cancer accelerated in vivo. CONCLUSIONS: These findings suggest that stress-related hormones affect the tumor progression of breast cancer. Therefore, strengthening the emotional management strategies of patients during the process of antitumor treatment as a supplement to the existing treatments may be beneficial. AME Publishing Company 2021-01 /pmc/articles/PMC7867925/ /pubmed/33569451 http://dx.doi.org/10.21037/atm-20-8176 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Zhu, Zhen
Yu, Ruihua
Yang, Chao
Li, Dong
Wang, Jiawei
Yang, Wanli
Ji, Yonghua
Wang, Li
Wang, Yaosheng
Jiang, Feng
Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
title Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
title_full Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
title_fullStr Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
title_full_unstemmed Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
title_short Stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
title_sort stress-related hormone reduces autophagy through the regulation of phosphatidylethanolamine in breast cancer cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867925/
https://www.ncbi.nlm.nih.gov/pubmed/33569451
http://dx.doi.org/10.21037/atm-20-8176
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