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WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling

INTRODUCTION: A number of evidences have proved that “Nostoc commune” Vauch can improve human immunity and prevent diseases, however, the specific mechanism remains unclear. The biological activity of the main protein component of “Nostoc commune” Vauch extracellular matrix– a water-stress protein (...

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Autores principales: Chen, Xiaoxia, Bai, Wenqi, Liu, Xiangrong, Zhao, Jiao, Li, Zhiyuan, Li, Jianrong, Su, Liping, Guan, Tao, Sun, Ruifang, Yang, Xihua, Lv, Caixia, Wang, Zhixiang, Hu, Linjie, Li, Zheng, Ma, Jinfeng, Zhang, Huanhu, Lu, Xiaoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9779803/
https://www.ncbi.nlm.nih.gov/pubmed/36568183
http://dx.doi.org/10.3389/fonc.2022.1012863
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author Chen, Xiaoxia
Bai, Wenqi
Liu, Xiangrong
Zhao, Jiao
Li, Zhiyuan
Li, Jianrong
Su, Liping
Guan, Tao
Sun, Ruifang
Yang, Xihua
Lv, Caixia
Wang, Zhixiang
Hu, Linjie
Li, Zheng
Ma, Jinfeng
Zhang, Huanhu
Lu, Xiaoqing
author_facet Chen, Xiaoxia
Bai, Wenqi
Liu, Xiangrong
Zhao, Jiao
Li, Zhiyuan
Li, Jianrong
Su, Liping
Guan, Tao
Sun, Ruifang
Yang, Xihua
Lv, Caixia
Wang, Zhixiang
Hu, Linjie
Li, Zheng
Ma, Jinfeng
Zhang, Huanhu
Lu, Xiaoqing
author_sort Chen, Xiaoxia
collection PubMed
description INTRODUCTION: A number of evidences have proved that “Nostoc commune” Vauch can improve human immunity and prevent diseases, however, the specific mechanism remains unclear. The biological activity of the main protein component of “Nostoc commune” Vauch extracellular matrix– a water-stress protein (WSP) still needs to be elucidated. METHODS: In our study, we validated the role of WSP in gastric cancer metastasis at the cellular level, the organoid level and in mouse models, and also studied the role of EGFRVIII and downstream signaling molecules after WSP treatment. RESULTS: We found that WSP can significantly inhibit the metastasis of gastric cancer cells. Interestingly, we found that the anti-metastasis ability of WSP on gastric cancer was related to membrane protein receptor EGFRVIII, which was realized by inhibiting the downstream EGFRVIII signaling pathway. In terms of mechanism, WSP can inhibit the downstream EGFRVIII signaling pathway Akt-PI3K and further inhibit the secretion of cancer-related metastasis proteins such as MMP2 and MMP9, thus, significantly affecting the metastasis of gastric cancer cells. DISCUSSION: Given the anticancer properties of WSP, drug developers and manufacturers can further develop protein drugs for cancer patients using protein engineering techniques based on the properties of WSP.
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spelling pubmed-97798032022-12-23 WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling Chen, Xiaoxia Bai, Wenqi Liu, Xiangrong Zhao, Jiao Li, Zhiyuan Li, Jianrong Su, Liping Guan, Tao Sun, Ruifang Yang, Xihua Lv, Caixia Wang, Zhixiang Hu, Linjie Li, Zheng Ma, Jinfeng Zhang, Huanhu Lu, Xiaoqing Front Oncol Oncology INTRODUCTION: A number of evidences have proved that “Nostoc commune” Vauch can improve human immunity and prevent diseases, however, the specific mechanism remains unclear. The biological activity of the main protein component of “Nostoc commune” Vauch extracellular matrix– a water-stress protein (WSP) still needs to be elucidated. METHODS: In our study, we validated the role of WSP in gastric cancer metastasis at the cellular level, the organoid level and in mouse models, and also studied the role of EGFRVIII and downstream signaling molecules after WSP treatment. RESULTS: We found that WSP can significantly inhibit the metastasis of gastric cancer cells. Interestingly, we found that the anti-metastasis ability of WSP on gastric cancer was related to membrane protein receptor EGFRVIII, which was realized by inhibiting the downstream EGFRVIII signaling pathway. In terms of mechanism, WSP can inhibit the downstream EGFRVIII signaling pathway Akt-PI3K and further inhibit the secretion of cancer-related metastasis proteins such as MMP2 and MMP9, thus, significantly affecting the metastasis of gastric cancer cells. DISCUSSION: Given the anticancer properties of WSP, drug developers and manufacturers can further develop protein drugs for cancer patients using protein engineering techniques based on the properties of WSP. Frontiers Media S.A. 2022-12-08 /pmc/articles/PMC9779803/ /pubmed/36568183 http://dx.doi.org/10.3389/fonc.2022.1012863 Text en Copyright © 2022 Chen, Bai, Liu, Zhao, Li, Li, Su, Guan, Sun, Yang, Lv, Wang, Hu, Li, Ma, Zhang and Lu https://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 Oncology
Chen, Xiaoxia
Bai, Wenqi
Liu, Xiangrong
Zhao, Jiao
Li, Zhiyuan
Li, Jianrong
Su, Liping
Guan, Tao
Sun, Ruifang
Yang, Xihua
Lv, Caixia
Wang, Zhixiang
Hu, Linjie
Li, Zheng
Ma, Jinfeng
Zhang, Huanhu
Lu, Xiaoqing
WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling
title WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling
title_full WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling
title_fullStr WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling
title_full_unstemmed WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling
title_short WSP from “Nostoc commune” Vauch. suppresses gastric cancer migration via EGFRVIII signaling
title_sort wsp from “nostoc commune” vauch. suppresses gastric cancer migration via egfrviii signaling
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9779803/
https://www.ncbi.nlm.nih.gov/pubmed/36568183
http://dx.doi.org/10.3389/fonc.2022.1012863
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