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Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation

[Image: see text] Esophageal squamous cell carcinoma (ESCC) is a malignant epithelial cancer of the esophageal epithelium. Piezo-type mechanosensitive ion channel component 1 (Piezo1), an essential mechanosensitive protein, plays an important role in maintaining cell biological functions under the s...

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Autores principales: Gao, Lu, Ji, Yun, Wang, Lulu, He, Meixia, Yang, Xiaojing, Qiu, Yibing, Sun, Xu, Ji, Zhenyu, Yang, Guanrui, Zhang, Jianying, Li, Shanshan, Dai, Liping, Zhang, Liguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153669/
https://www.ncbi.nlm.nih.gov/pubmed/34056174
http://dx.doi.org/10.1021/acsomega.1c00505
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author Gao, Lu
Ji, Yun
Wang, Lulu
He, Meixia
Yang, Xiaojing
Qiu, Yibing
Sun, Xu
Ji, Zhenyu
Yang, Guanrui
Zhang, Jianying
Li, Shanshan
Dai, Liping
Zhang, Liguo
author_facet Gao, Lu
Ji, Yun
Wang, Lulu
He, Meixia
Yang, Xiaojing
Qiu, Yibing
Sun, Xu
Ji, Zhenyu
Yang, Guanrui
Zhang, Jianying
Li, Shanshan
Dai, Liping
Zhang, Liguo
author_sort Gao, Lu
collection PubMed
description [Image: see text] Esophageal squamous cell carcinoma (ESCC) is a malignant epithelial cancer of the esophageal epithelium. Piezo-type mechanosensitive ion channel component 1 (Piezo1), an essential mechanosensitive protein, plays an important role in maintaining cell biological functions under the stimulation of physiological force. Immunohistochemical and bioinformatic analyses of ESCC tissue samples indicate that Piezo1 expression is higher in ESCC tissues than in paracancerous tissues. shRNA-mediated Piezo1 downregulation in the ESCC lines EC9706 and EC109 showed that proliferation, migration, and invasion were suppressed by Piezo1 knockdown. Piezo1 downregulation suppresses ESCC migration and invasion in both cells and tissues via the epithelial–mesenchymal transition pathway. Moreover, G0/G1 to S-phase cell cycle progression was inhibited, and cell apoptosis was induced by Piezo1 downregulation. Furthermore, we observed an interaction between Piezo1 and p53 using immunoprecipitation. The protein levels of p53, downstream factor Bax, apoptosis executioner cleaved-caspase3, and caspase3 were significantly upregulated by the downregulation of Piezo1. The inhibited growth rate and upregulated expression of these related factors were validated using tumor-bearing mice. Therefore, Piezo1 downregulation induces ESCC apoptosis via a Piezo1–p53–Bax–Caspase 3 axis. In conclusion, Piezo1 downregulation suppresses ESCC development, and mechanosensitive protein Piezo1 can be considered a new target for ESCC therapy.
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spelling pubmed-81536692021-05-27 Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation Gao, Lu Ji, Yun Wang, Lulu He, Meixia Yang, Xiaojing Qiu, Yibing Sun, Xu Ji, Zhenyu Yang, Guanrui Zhang, Jianying Li, Shanshan Dai, Liping Zhang, Liguo ACS Omega [Image: see text] Esophageal squamous cell carcinoma (ESCC) is a malignant epithelial cancer of the esophageal epithelium. Piezo-type mechanosensitive ion channel component 1 (Piezo1), an essential mechanosensitive protein, plays an important role in maintaining cell biological functions under the stimulation of physiological force. Immunohistochemical and bioinformatic analyses of ESCC tissue samples indicate that Piezo1 expression is higher in ESCC tissues than in paracancerous tissues. shRNA-mediated Piezo1 downregulation in the ESCC lines EC9706 and EC109 showed that proliferation, migration, and invasion were suppressed by Piezo1 knockdown. Piezo1 downregulation suppresses ESCC migration and invasion in both cells and tissues via the epithelial–mesenchymal transition pathway. Moreover, G0/G1 to S-phase cell cycle progression was inhibited, and cell apoptosis was induced by Piezo1 downregulation. Furthermore, we observed an interaction between Piezo1 and p53 using immunoprecipitation. The protein levels of p53, downstream factor Bax, apoptosis executioner cleaved-caspase3, and caspase3 were significantly upregulated by the downregulation of Piezo1. The inhibited growth rate and upregulated expression of these related factors were validated using tumor-bearing mice. Therefore, Piezo1 downregulation induces ESCC apoptosis via a Piezo1–p53–Bax–Caspase 3 axis. In conclusion, Piezo1 downregulation suppresses ESCC development, and mechanosensitive protein Piezo1 can be considered a new target for ESCC therapy. American Chemical Society 2021-04-12 /pmc/articles/PMC8153669/ /pubmed/34056174 http://dx.doi.org/10.1021/acsomega.1c00505 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Gao, Lu
Ji, Yun
Wang, Lulu
He, Meixia
Yang, Xiaojing
Qiu, Yibing
Sun, Xu
Ji, Zhenyu
Yang, Guanrui
Zhang, Jianying
Li, Shanshan
Dai, Liping
Zhang, Liguo
Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation
title Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation
title_full Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation
title_fullStr Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation
title_full_unstemmed Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation
title_short Suppression of Esophageal Squamous Cell Carcinoma Development by Mechanosensitive Protein Piezo1 Downregulation
title_sort suppression of esophageal squamous cell carcinoma development by mechanosensitive protein piezo1 downregulation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153669/
https://www.ncbi.nlm.nih.gov/pubmed/34056174
http://dx.doi.org/10.1021/acsomega.1c00505
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