Antimicrobial agent chloroxylenol targets [beta]-catenin-mediated Wnt signaling and exerts anticancer activity in colorectal cancer
Chloroxylenol is the active ingredient of the antibacterial agent Dettol. The anticancer effect and underlying mechanisms of this compound and other common antimicrobial agents have not been clearly elucidated. In the present study, the effects of chloroxylenol, benzalkonium chloride, benzethonium c...
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Veröffentlicht in: | International journal of oncology 2023-11, Vol.63 (5), p.1 |
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creator | Sun, Qi Liu, Boxin Lan, Quanxue Su, Zijie Fu, Qiuxia Wang, Lian Deng, Yingying Li, Chuanli Xue, Vivian Weiwen Liu, Shanshan Chen, Xianxiong Yang, Guowu Lu, Desheng |
description | Chloroxylenol is the active ingredient of the antibacterial agent Dettol. The anticancer effect and underlying mechanisms of this compound and other common antimicrobial agents have not been clearly elucidated. In the present study, the effects of chloroxylenol, benzalkonium chloride, benzethonium chloride, triclosan and triclocarban on [beta]-catenin-mediated Wnt signaling in colorectal cancer were evaluated using the SuperTOPFlash reporter assay. It was demonstrated that chloroxylenol, but not the other antimicrobial agents tested, inhibited the Wnt/[beta]-catenin signaling pathway by decreasing the nuclear translocation of [beta]-catenin and disrupting [beta]-catenin/T-cell factor 4 complex, which resulted in the downregulation of the Wnt target genes Axin2, Survivin and Leucine-rich G protein-coupled receptor-5. Chloroxylenol effectively inhibited the viability, proliferation, migration and invasion, and sphere formation, and induced apoptosis in HCT116 and SW480 cells. Notably, chloroxylenol attenuated the growth of colorectal cancer in the MC38 cell xenograft model and inhibited organoid formation by the patient-derived cells. Chloroxylenol also demonstrated inhibitory effects on the stemness of colorectal cancer cells. The results of the present study demonstrated that chloroxylenol could exert anti-tumor activities in colorectal cancer by targeting the Wnt/[beta]-catenin signaling pathway, which provided an insight into its therapeutic potential as an anticancer agent. Key words: chloroxylenol, Wnt/[beta]-catenin signaling pathway, [beta]-catenin/T-cell factor 4, colorectal cancer |
doi_str_mv | 10.3892/ijo.2023.5569 |
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The anticancer effect and underlying mechanisms of this compound and other common antimicrobial agents have not been clearly elucidated. In the present study, the effects of chloroxylenol, benzalkonium chloride, benzethonium chloride, triclosan and triclocarban on [beta]-catenin-mediated Wnt signaling in colorectal cancer were evaluated using the SuperTOPFlash reporter assay. It was demonstrated that chloroxylenol, but not the other antimicrobial agents tested, inhibited the Wnt/[beta]-catenin signaling pathway by decreasing the nuclear translocation of [beta]-catenin and disrupting [beta]-catenin/T-cell factor 4 complex, which resulted in the downregulation of the Wnt target genes Axin2, Survivin and Leucine-rich G protein-coupled receptor-5. Chloroxylenol effectively inhibited the viability, proliferation, migration and invasion, and sphere formation, and induced apoptosis in HCT116 and SW480 cells. Notably, chloroxylenol attenuated the growth of colorectal cancer in the MC38 cell xenograft model and inhibited organoid formation by the patient-derived cells. Chloroxylenol also demonstrated inhibitory effects on the stemness of colorectal cancer cells. The results of the present study demonstrated that chloroxylenol could exert anti-tumor activities in colorectal cancer by targeting the Wnt/[beta]-catenin signaling pathway, which provided an insight into its therapeutic potential as an anticancer agent. Key words: chloroxylenol, Wnt/[beta]-catenin signaling pathway, [beta]-catenin/T-cell factor 4, colorectal cancer</description><identifier>ISSN: 1019-6439</identifier><identifier>DOI: 10.3892/ijo.2023.5569</identifier><language>eng</language><publisher>Spandidos Publications</publisher><subject>Cancer ; Care and treatment ; Colorectal cancer ; Ethylenediaminetetraacetic acid ; G proteins ; Genetic aspects ; Health aspects ; Membrane proteins ; Oncology, Experimental ; Surface active agents</subject><ispartof>International journal of oncology, 2023-11, Vol.63 (5), p.1</ispartof><rights>COPYRIGHT 2023 Spandidos Publications</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sun, Qi</creatorcontrib><creatorcontrib>Liu, Boxin</creatorcontrib><creatorcontrib>Lan, Quanxue</creatorcontrib><creatorcontrib>Su, Zijie</creatorcontrib><creatorcontrib>Fu, Qiuxia</creatorcontrib><creatorcontrib>Wang, Lian</creatorcontrib><creatorcontrib>Deng, Yingying</creatorcontrib><creatorcontrib>Li, Chuanli</creatorcontrib><creatorcontrib>Xue, Vivian Weiwen</creatorcontrib><creatorcontrib>Liu, Shanshan</creatorcontrib><creatorcontrib>Chen, Xianxiong</creatorcontrib><creatorcontrib>Yang, Guowu</creatorcontrib><creatorcontrib>Lu, Desheng</creatorcontrib><title>Antimicrobial agent chloroxylenol targets [beta]-catenin-mediated Wnt signaling and exerts anticancer activity in colorectal cancer</title><title>International journal of oncology</title><description>Chloroxylenol is the active ingredient of the antibacterial agent Dettol. The anticancer effect and underlying mechanisms of this compound and other common antimicrobial agents have not been clearly elucidated. In the present study, the effects of chloroxylenol, benzalkonium chloride, benzethonium chloride, triclosan and triclocarban on [beta]-catenin-mediated Wnt signaling in colorectal cancer were evaluated using the SuperTOPFlash reporter assay. It was demonstrated that chloroxylenol, but not the other antimicrobial agents tested, inhibited the Wnt/[beta]-catenin signaling pathway by decreasing the nuclear translocation of [beta]-catenin and disrupting [beta]-catenin/T-cell factor 4 complex, which resulted in the downregulation of the Wnt target genes Axin2, Survivin and Leucine-rich G protein-coupled receptor-5. Chloroxylenol effectively inhibited the viability, proliferation, migration and invasion, and sphere formation, and induced apoptosis in HCT116 and SW480 cells. Notably, chloroxylenol attenuated the growth of colorectal cancer in the MC38 cell xenograft model and inhibited organoid formation by the patient-derived cells. Chloroxylenol also demonstrated inhibitory effects on the stemness of colorectal cancer cells. The results of the present study demonstrated that chloroxylenol could exert anti-tumor activities in colorectal cancer by targeting the Wnt/[beta]-catenin signaling pathway, which provided an insight into its therapeutic potential as an anticancer agent. Key words: chloroxylenol, Wnt/[beta]-catenin signaling pathway, [beta]-catenin/T-cell factor 4, colorectal cancer</description><subject>Cancer</subject><subject>Care and treatment</subject><subject>Colorectal cancer</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>G proteins</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Membrane proteins</subject><subject>Oncology, Experimental</subject><subject>Surface active agents</subject><issn>1019-6439</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptkM1LAzEQxXNQsFaP3gOCt63JZrPZHEvxCwpeCh5ESnZ2dpuSJrCJ0p79xw3UQwWZwwxv3u8NDCE3nM1Eo8t7uw2zkpViJmWtz8iEM66LuhL6glzGuGWslJLxCfme-2R3FsbQWuOoGdAnChsXxrA_OPTB0WTGAVOk7y0m81GASeitL3bY2Tx29C0T0Q7eOOsHanxHcY9jBkyOBuMBR2og2S-bDtR6CiGnI6R87ri9Iue9cRGvf_uUrB4fVovnYvn69LKYL4tBN7oQkhvWVy30WqKqSwRZMc7ruuTIUFVC8abpOt62qm7ASKF60C1nwAG44L2Ykttj7GAcrq3vQxoN7GyE9VwpIauqUjq7Zv-4cnWY3xQ89jbrf4C7E2CDxqVNDO4z2eDjqfEHOIZ_PA</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Sun, Qi</creator><creator>Liu, Boxin</creator><creator>Lan, Quanxue</creator><creator>Su, Zijie</creator><creator>Fu, Qiuxia</creator><creator>Wang, Lian</creator><creator>Deng, Yingying</creator><creator>Li, Chuanli</creator><creator>Xue, Vivian Weiwen</creator><creator>Liu, Shanshan</creator><creator>Chen, Xianxiong</creator><creator>Yang, Guowu</creator><creator>Lu, Desheng</creator><general>Spandidos Publications</general><scope/></search><sort><creationdate>20231101</creationdate><title>Antimicrobial agent chloroxylenol targets [beta]-catenin-mediated Wnt signaling and exerts anticancer activity in colorectal cancer</title><author>Sun, Qi ; Liu, Boxin ; Lan, Quanxue ; Su, Zijie ; Fu, Qiuxia ; Wang, Lian ; Deng, Yingying ; Li, Chuanli ; Xue, Vivian Weiwen ; Liu, Shanshan ; Chen, Xianxiong ; Yang, Guowu ; Lu, Desheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g989-351a0f4bcf95e762ec540116621e0e7437188dd1bb768ca537fc9b10c1cc131f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cancer</topic><topic>Care and treatment</topic><topic>Colorectal cancer</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>G proteins</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Membrane proteins</topic><topic>Oncology, Experimental</topic><topic>Surface active agents</topic><toplevel>online_resources</toplevel><creatorcontrib>Sun, Qi</creatorcontrib><creatorcontrib>Liu, Boxin</creatorcontrib><creatorcontrib>Lan, Quanxue</creatorcontrib><creatorcontrib>Su, Zijie</creatorcontrib><creatorcontrib>Fu, Qiuxia</creatorcontrib><creatorcontrib>Wang, Lian</creatorcontrib><creatorcontrib>Deng, Yingying</creatorcontrib><creatorcontrib>Li, Chuanli</creatorcontrib><creatorcontrib>Xue, Vivian Weiwen</creatorcontrib><creatorcontrib>Liu, Shanshan</creatorcontrib><creatorcontrib>Chen, Xianxiong</creatorcontrib><creatorcontrib>Yang, Guowu</creatorcontrib><creatorcontrib>Lu, Desheng</creatorcontrib><jtitle>International journal of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Qi</au><au>Liu, Boxin</au><au>Lan, Quanxue</au><au>Su, Zijie</au><au>Fu, Qiuxia</au><au>Wang, Lian</au><au>Deng, Yingying</au><au>Li, Chuanli</au><au>Xue, Vivian Weiwen</au><au>Liu, Shanshan</au><au>Chen, Xianxiong</au><au>Yang, Guowu</au><au>Lu, Desheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial agent chloroxylenol targets [beta]-catenin-mediated Wnt signaling and exerts anticancer activity in colorectal cancer</atitle><jtitle>International journal of oncology</jtitle><date>2023-11-01</date><risdate>2023</risdate><volume>63</volume><issue>5</issue><spage>1</spage><pages>1-</pages><issn>1019-6439</issn><abstract>Chloroxylenol is the active ingredient of the antibacterial agent Dettol. The anticancer effect and underlying mechanisms of this compound and other common antimicrobial agents have not been clearly elucidated. In the present study, the effects of chloroxylenol, benzalkonium chloride, benzethonium chloride, triclosan and triclocarban on [beta]-catenin-mediated Wnt signaling in colorectal cancer were evaluated using the SuperTOPFlash reporter assay. It was demonstrated that chloroxylenol, but not the other antimicrobial agents tested, inhibited the Wnt/[beta]-catenin signaling pathway by decreasing the nuclear translocation of [beta]-catenin and disrupting [beta]-catenin/T-cell factor 4 complex, which resulted in the downregulation of the Wnt target genes Axin2, Survivin and Leucine-rich G protein-coupled receptor-5. Chloroxylenol effectively inhibited the viability, proliferation, migration and invasion, and sphere formation, and induced apoptosis in HCT116 and SW480 cells. Notably, chloroxylenol attenuated the growth of colorectal cancer in the MC38 cell xenograft model and inhibited organoid formation by the patient-derived cells. Chloroxylenol also demonstrated inhibitory effects on the stemness of colorectal cancer cells. The results of the present study demonstrated that chloroxylenol could exert anti-tumor activities in colorectal cancer by targeting the Wnt/[beta]-catenin signaling pathway, which provided an insight into its therapeutic potential as an anticancer agent. Key words: chloroxylenol, Wnt/[beta]-catenin signaling pathway, [beta]-catenin/T-cell factor 4, colorectal cancer</abstract><pub>Spandidos Publications</pub><doi>10.3892/ijo.2023.5569</doi></addata></record> |
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subjects | Cancer Care and treatment Colorectal cancer Ethylenediaminetetraacetic acid G proteins Genetic aspects Health aspects Membrane proteins Oncology, Experimental Surface active agents |
title | Antimicrobial agent chloroxylenol targets [beta]-catenin-mediated Wnt signaling and exerts anticancer activity in colorectal cancer |
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