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Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma
Gender differences in esophageal cancer patients indicate that estradiol may have antitumor effects on esophageal cancer. The initiation of endoplasmic reticulum stress (ERS) can induce apoptosis in esophageal cancer cells. However, it is still unknown whether estradiol inhibits the development of e...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387645/ https://www.ncbi.nlm.nih.gov/pubmed/32793111 http://dx.doi.org/10.3389/fendo.2020.00410 |
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author | Wang, Chen Wang, Peng Liu, Jun-Chao Zhao, Zhen-Ao Guo, Rui Li, Ying Liu, Ya-Sen Li, Shu-Guang Zhao, Zi-Gang |
author_facet | Wang, Chen Wang, Peng Liu, Jun-Chao Zhao, Zhen-Ao Guo, Rui Li, Ying Liu, Ya-Sen Li, Shu-Guang Zhao, Zi-Gang |
author_sort | Wang, Chen |
collection | PubMed |
description | Gender differences in esophageal cancer patients indicate that estradiol may have antitumor effects on esophageal cancer. The initiation of endoplasmic reticulum stress (ERS) can induce apoptosis in esophageal cancer cells. However, it is still unknown whether estradiol inhibits the development of esophageal cancer by activating ERS pathway. In this study, the gender difference in the development of esophageal cancer was observed by analyzing clinical data and the experimental tumor xenografts in mice. Meanwhile, we investigated the mechanism of ERS in estradiol-mediated inhibition of esophageal cancer using esophageal squamous cell carcinoma cell line EC109. The proportion of male patients with esophageal cancer was significantly higher than female patients. Meanwhile, male patients were prone to have adventitial invasion. The weight of transplanted tumors in female mice was significantly smaller than that in male mice. In vitro experiments showed estradiol inhibits the viability and migration of EC109 cells by increasing the expression of ERS-related proteins, whereas ERS inhibitor 4-PBA abolished the effects of estradiol. In conclusion, our data demonstrate that sex difference exists in the occurrence of esophageal cancer. Estradiol can inhibit the viability and migration of esophageal cancer cells through the activation of ERS, providing a novel insight for esophageal cancer development, treatment, and prevention. |
format | Online Article Text |
id | pubmed-7387645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73876452020-08-12 Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma Wang, Chen Wang, Peng Liu, Jun-Chao Zhao, Zhen-Ao Guo, Rui Li, Ying Liu, Ya-Sen Li, Shu-Guang Zhao, Zi-Gang Front Endocrinol (Lausanne) Endocrinology Gender differences in esophageal cancer patients indicate that estradiol may have antitumor effects on esophageal cancer. The initiation of endoplasmic reticulum stress (ERS) can induce apoptosis in esophageal cancer cells. However, it is still unknown whether estradiol inhibits the development of esophageal cancer by activating ERS pathway. In this study, the gender difference in the development of esophageal cancer was observed by analyzing clinical data and the experimental tumor xenografts in mice. Meanwhile, we investigated the mechanism of ERS in estradiol-mediated inhibition of esophageal cancer using esophageal squamous cell carcinoma cell line EC109. The proportion of male patients with esophageal cancer was significantly higher than female patients. Meanwhile, male patients were prone to have adventitial invasion. The weight of transplanted tumors in female mice was significantly smaller than that in male mice. In vitro experiments showed estradiol inhibits the viability and migration of EC109 cells by increasing the expression of ERS-related proteins, whereas ERS inhibitor 4-PBA abolished the effects of estradiol. In conclusion, our data demonstrate that sex difference exists in the occurrence of esophageal cancer. Estradiol can inhibit the viability and migration of esophageal cancer cells through the activation of ERS, providing a novel insight for esophageal cancer development, treatment, and prevention. Frontiers Media S.A. 2020-07-22 /pmc/articles/PMC7387645/ /pubmed/32793111 http://dx.doi.org/10.3389/fendo.2020.00410 Text en Copyright © 2020 Wang, Wang, Liu, Zhao, Guo, Li, Liu, Li and Zhao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Wang, Chen Wang, Peng Liu, Jun-Chao Zhao, Zhen-Ao Guo, Rui Li, Ying Liu, Ya-Sen Li, Shu-Guang Zhao, Zi-Gang Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma |
title | Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma |
title_full | Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma |
title_fullStr | Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma |
title_full_unstemmed | Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma |
title_short | Interaction of Estradiol and Endoplasmic Reticulum Stress in the Development of Esophageal Carcinoma |
title_sort | interaction of estradiol and endoplasmic reticulum stress in the development of esophageal carcinoma |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387645/ https://www.ncbi.nlm.nih.gov/pubmed/32793111 http://dx.doi.org/10.3389/fendo.2020.00410 |
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