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Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway

Colorectal cancer (CRC) is a common clinical malignant tumor and closely related to intestinal microbiome disorders. Especially, Fusobacterium nucleatum (F. nucleatum) is one of the most prevalent pathogens in CRC. However, its change in CRC patients of Northwest China, an area with a high incidence...

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Autores principales: Zhou, Zhongkun, Wang, Yiqing, Ji, Rui, Zhang, Dekui, Ma, Chi, Ma, Wantong, Ma, Yunhao, Jiang, Xinrong, Du, Kangjia, Zhang, Rentao, Chen, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931468/
https://www.ncbi.nlm.nih.gov/pubmed/35308221
http://dx.doi.org/10.3389/fphar.2022.841918
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author Zhou, Zhongkun
Wang, Yiqing
Ji, Rui
Zhang, Dekui
Ma, Chi
Ma, Wantong
Ma, Yunhao
Jiang, Xinrong
Du, Kangjia
Zhang, Rentao
Chen, Peng
author_facet Zhou, Zhongkun
Wang, Yiqing
Ji, Rui
Zhang, Dekui
Ma, Chi
Ma, Wantong
Ma, Yunhao
Jiang, Xinrong
Du, Kangjia
Zhang, Rentao
Chen, Peng
author_sort Zhou, Zhongkun
collection PubMed
description Colorectal cancer (CRC) is a common clinical malignant tumor and closely related to intestinal microbiome disorders. Especially, Fusobacterium nucleatum (F. nucleatum) is one of the most prevalent pathogens in CRC. However, its change in CRC patients of Northwest China, an area with a high incidence of gastrointestinal tumors, is unclear, and therapeutic strategies targeting F. nucleatum remain unresolved. Here, fecal samples of healthy people and CRC patients were studied using 16S rRNA sequencing to explore microbial community alterations. Additionally, vanillin derivate (IPM711 and IPM712) intervention by coculture with CRC cells and potential mechanism were investigated. Results showed that intestinal microbial homeostasis was gradually dysregulated, and the abundance of Fusobacterium was higher in CRC patients. Moreover, IPM711 and IPM712 showed better anti-F. nucleatum activity than vanillin by increasing cell membrane permeability and destroying bacterial integrity. In addition, IPM711 and IPM712 could downregulate the expression of E-cadherin and β-catenin, thus, suppressing the migration of HCT116. Collectively, IPM711 and IPM712 have both anticolorectal cancer and anti-F. nucleatum activities, providing potential natural product drug candidates for microbe-targeted strategies for the treatment of CRC.
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spelling pubmed-89314682022-03-19 Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway Zhou, Zhongkun Wang, Yiqing Ji, Rui Zhang, Dekui Ma, Chi Ma, Wantong Ma, Yunhao Jiang, Xinrong Du, Kangjia Zhang, Rentao Chen, Peng Front Pharmacol Pharmacology Colorectal cancer (CRC) is a common clinical malignant tumor and closely related to intestinal microbiome disorders. Especially, Fusobacterium nucleatum (F. nucleatum) is one of the most prevalent pathogens in CRC. However, its change in CRC patients of Northwest China, an area with a high incidence of gastrointestinal tumors, is unclear, and therapeutic strategies targeting F. nucleatum remain unresolved. Here, fecal samples of healthy people and CRC patients were studied using 16S rRNA sequencing to explore microbial community alterations. Additionally, vanillin derivate (IPM711 and IPM712) intervention by coculture with CRC cells and potential mechanism were investigated. Results showed that intestinal microbial homeostasis was gradually dysregulated, and the abundance of Fusobacterium was higher in CRC patients. Moreover, IPM711 and IPM712 showed better anti-F. nucleatum activity than vanillin by increasing cell membrane permeability and destroying bacterial integrity. In addition, IPM711 and IPM712 could downregulate the expression of E-cadherin and β-catenin, thus, suppressing the migration of HCT116. Collectively, IPM711 and IPM712 have both anticolorectal cancer and anti-F. nucleatum activities, providing potential natural product drug candidates for microbe-targeted strategies for the treatment of CRC. Frontiers Media S.A. 2022-03-04 /pmc/articles/PMC8931468/ /pubmed/35308221 http://dx.doi.org/10.3389/fphar.2022.841918 Text en Copyright © 2022 Zhou, Wang, Ji, Zhang, Ma, Ma, Ma, Jiang, Du, Zhang and Chen. 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 Pharmacology
Zhou, Zhongkun
Wang, Yiqing
Ji, Rui
Zhang, Dekui
Ma, Chi
Ma, Wantong
Ma, Yunhao
Jiang, Xinrong
Du, Kangjia
Zhang, Rentao
Chen, Peng
Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway
title Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway
title_full Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway
title_fullStr Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway
title_full_unstemmed Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway
title_short Vanillin Derivatives Reverse Fusobacterium nucleatum-Induced Proliferation and Migration of Colorectal Cancer Through E-Cadherin/β-Catenin Pathway
title_sort vanillin derivatives reverse fusobacterium nucleatum-induced proliferation and migration of colorectal cancer through e-cadherin/β-catenin pathway
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931468/
https://www.ncbi.nlm.nih.gov/pubmed/35308221
http://dx.doi.org/10.3389/fphar.2022.841918
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