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Icariside II suppressed tumorigenesis by epigenetically regulating the circβ-catenin-Wnt/β-catenin axis in colorectal cancer
[Display omitted] •Icariside II induced apoptosis and cell cycle arrest in CRC cells.•Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling in CRC cells.•Icariside II suppressed the biogenesis of circβ-catenin via epigenetically targeti...
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Published in: | Bioorganic chemistry 2022-07, Vol.124, p.105800-105800, Article 105800 |
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creator | Shi, Chuan-Jian Li, Shi-Ying Shen, Chun-Hui Pan, Fei-Fei Deng, Li-Qiang Fu, Wei-Ming Wang, Ji-Yong Zhang, Jin-Fang |
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•Icariside II induced apoptosis and cell cycle arrest in CRC cells.•Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling in CRC cells.•Icariside II suppressed the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) in CRC cells.
Icariside II, a flavonol glycoside, one of the major components of Traditional Chinese Medicine Herba epimedii. In the present study, we found that Icariside II suppressed the proliferation of CRC by inducing cell cycle arrest and apoptosis in vitro and inhibited tumor growth in vivo. The further mechanism investigation showed that Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling. Circβ-catenin was considered as a promising candidate for mediating the tumorigenesis and the activation of Wnt/β-catenin signaling in CRC cells. Furthermore, Icariside II has been proven to suppress the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) to decrease global DNA methylation levels in CRC cells. Taken together, our results indicated that Icariside II suppressed tumorigenesis by epigenetically silencing the activation of circβ-catenin-Wnt/β-catenin axis in colorectal cancer. More importantly, the information gained from this study suggest that Icariside II may have great potential to be developed as a therapeutic drug for CRC patients. |
doi_str_mv | 10.1016/j.bioorg.2022.105800 |
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•Icariside II induced apoptosis and cell cycle arrest in CRC cells.•Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling in CRC cells.•Icariside II suppressed the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) in CRC cells.
Icariside II, a flavonol glycoside, one of the major components of Traditional Chinese Medicine Herba epimedii. In the present study, we found that Icariside II suppressed the proliferation of CRC by inducing cell cycle arrest and apoptosis in vitro and inhibited tumor growth in vivo. The further mechanism investigation showed that Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling. Circβ-catenin was considered as a promising candidate for mediating the tumorigenesis and the activation of Wnt/β-catenin signaling in CRC cells. Furthermore, Icariside II has been proven to suppress the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) to decrease global DNA methylation levels in CRC cells. Taken together, our results indicated that Icariside II suppressed tumorigenesis by epigenetically silencing the activation of circβ-catenin-Wnt/β-catenin axis in colorectal cancer. More importantly, the information gained from this study suggest that Icariside II may have great potential to be developed as a therapeutic drug for CRC patients.</description><identifier>ISSN: 0045-2068</identifier><identifier>EISSN: 1090-2120</identifier><identifier>DOI: 10.1016/j.bioorg.2022.105800</identifier><identifier>PMID: 35468415</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Circβ-catenin ; Colorectal cancer ; DNA methylation ; Icariside II ; Tumorigenesis ; Wnt/β-catenin signaling</subject><ispartof>Bioorganic chemistry, 2022-07, Vol.124, p.105800-105800, Article 105800</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-b4f851ba743b628cb19eeacc526ee4cf4ffd0a0ecf5ca892c8a8918b5c3f31be3</citedby><cites>FETCH-LOGICAL-c362t-b4f851ba743b628cb19eeacc526ee4cf4ffd0a0ecf5ca892c8a8918b5c3f31be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27898,27899</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35468415$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Chuan-Jian</creatorcontrib><creatorcontrib>Li, Shi-Ying</creatorcontrib><creatorcontrib>Shen, Chun-Hui</creatorcontrib><creatorcontrib>Pan, Fei-Fei</creatorcontrib><creatorcontrib>Deng, Li-Qiang</creatorcontrib><creatorcontrib>Fu, Wei-Ming</creatorcontrib><creatorcontrib>Wang, Ji-Yong</creatorcontrib><creatorcontrib>Zhang, Jin-Fang</creatorcontrib><title>Icariside II suppressed tumorigenesis by epigenetically regulating the circβ-catenin-Wnt/β-catenin axis in colorectal cancer</title><title>Bioorganic chemistry</title><addtitle>Bioorg Chem</addtitle><description>[Display omitted]
•Icariside II induced apoptosis and cell cycle arrest in CRC cells.•Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling in CRC cells.•Icariside II suppressed the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) in CRC cells.
Icariside II, a flavonol glycoside, one of the major components of Traditional Chinese Medicine Herba epimedii. In the present study, we found that Icariside II suppressed the proliferation of CRC by inducing cell cycle arrest and apoptosis in vitro and inhibited tumor growth in vivo. The further mechanism investigation showed that Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling. Circβ-catenin was considered as a promising candidate for mediating the tumorigenesis and the activation of Wnt/β-catenin signaling in CRC cells. Furthermore, Icariside II has been proven to suppress the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) to decrease global DNA methylation levels in CRC cells. Taken together, our results indicated that Icariside II suppressed tumorigenesis by epigenetically silencing the activation of circβ-catenin-Wnt/β-catenin axis in colorectal cancer. More importantly, the information gained from this study suggest that Icariside II may have great potential to be developed as a therapeutic drug for CRC patients.</description><subject>Circβ-catenin</subject><subject>Colorectal cancer</subject><subject>DNA methylation</subject><subject>Icariside II</subject><subject>Tumorigenesis</subject><subject>Wnt/β-catenin signaling</subject><issn>0045-2068</issn><issn>1090-2120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kMFu1DAQhi3Uim4Lb4CQj71kazu2m70goQroSpW4tOJo2ZPJ4lU2DrZTdS99KB6EZ6q3KfTGZUYz-v9_NB8hHzhbcsb1xXbpfAhxsxRMiLJSDWNvyIKzFasEF-yILBiTqhJMNyfkNKUtY5zLS_2WnNRK6kZytSCPa7DRJ98iXa9pmsYxYkrY0jztQvQbHDD5RN2e4vg8ZQ-27_c04mbqbfbDhuafSMFH-PO7Aptx8EP1Y8gXryO1DyWjdAh9iAjZ9hTsABjfkePO9gnfv_Qzcvf1y-3VdXXz_dv66vNNBbUWuXKyaxR39lLWTosGHF8hWgAlNKKETnZdyyxD6BTYZiWgKZU3TkHd1dxhfUbO59wxhl8Tpmx2PgH2vR0wTMkIrZTSnAlZpHKWQgwpRezMGP3Oxr3hzBzIm62ZyZsDeTOTL7aPLxcmt8P2n-kv6iL4NAuw_HnvMZoEHguE1h-QmDb4_194AiyYm4Y</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Shi, Chuan-Jian</creator><creator>Li, Shi-Ying</creator><creator>Shen, Chun-Hui</creator><creator>Pan, Fei-Fei</creator><creator>Deng, Li-Qiang</creator><creator>Fu, Wei-Ming</creator><creator>Wang, Ji-Yong</creator><creator>Zhang, Jin-Fang</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20220701</creationdate><title>Icariside II suppressed tumorigenesis by epigenetically regulating the circβ-catenin-Wnt/β-catenin axis in colorectal cancer</title><author>Shi, Chuan-Jian ; Li, Shi-Ying ; Shen, Chun-Hui ; Pan, Fei-Fei ; Deng, Li-Qiang ; Fu, Wei-Ming ; Wang, Ji-Yong ; Zhang, Jin-Fang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-b4f851ba743b628cb19eeacc526ee4cf4ffd0a0ecf5ca892c8a8918b5c3f31be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Circβ-catenin</topic><topic>Colorectal cancer</topic><topic>DNA methylation</topic><topic>Icariside II</topic><topic>Tumorigenesis</topic><topic>Wnt/β-catenin signaling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Chuan-Jian</creatorcontrib><creatorcontrib>Li, Shi-Ying</creatorcontrib><creatorcontrib>Shen, Chun-Hui</creatorcontrib><creatorcontrib>Pan, Fei-Fei</creatorcontrib><creatorcontrib>Deng, Li-Qiang</creatorcontrib><creatorcontrib>Fu, Wei-Ming</creatorcontrib><creatorcontrib>Wang, Ji-Yong</creatorcontrib><creatorcontrib>Zhang, Jin-Fang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Chuan-Jian</au><au>Li, Shi-Ying</au><au>Shen, Chun-Hui</au><au>Pan, Fei-Fei</au><au>Deng, Li-Qiang</au><au>Fu, Wei-Ming</au><au>Wang, Ji-Yong</au><au>Zhang, Jin-Fang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Icariside II suppressed tumorigenesis by epigenetically regulating the circβ-catenin-Wnt/β-catenin axis in colorectal cancer</atitle><jtitle>Bioorganic chemistry</jtitle><addtitle>Bioorg Chem</addtitle><date>2022-07-01</date><risdate>2022</risdate><volume>124</volume><spage>105800</spage><epage>105800</epage><pages>105800-105800</pages><artnum>105800</artnum><issn>0045-2068</issn><eissn>1090-2120</eissn><abstract>[Display omitted]
•Icariside II induced apoptosis and cell cycle arrest in CRC cells.•Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling in CRC cells.•Icariside II suppressed the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) in CRC cells.
Icariside II, a flavonol glycoside, one of the major components of Traditional Chinese Medicine Herba epimedii. In the present study, we found that Icariside II suppressed the proliferation of CRC by inducing cell cycle arrest and apoptosis in vitro and inhibited tumor growth in vivo. The further mechanism investigation showed that Icariside II suppressed the expression of β-catenin and led to the functional inactivation of Wnt/β-catenin signaling. Circβ-catenin was considered as a promising candidate for mediating the tumorigenesis and the activation of Wnt/β-catenin signaling in CRC cells. Furthermore, Icariside II has been proven to suppress the biogenesis of circβ-catenin via epigenetically targeting DNA methyltransferases (DNMTs) to decrease global DNA methylation levels in CRC cells. Taken together, our results indicated that Icariside II suppressed tumorigenesis by epigenetically silencing the activation of circβ-catenin-Wnt/β-catenin axis in colorectal cancer. More importantly, the information gained from this study suggest that Icariside II may have great potential to be developed as a therapeutic drug for CRC patients.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>35468415</pmid><doi>10.1016/j.bioorg.2022.105800</doi><tpages>1</tpages></addata></record> |
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subjects | Circβ-catenin Colorectal cancer DNA methylation Icariside II Tumorigenesis Wnt/β-catenin signaling |
title | Icariside II suppressed tumorigenesis by epigenetically regulating the circβ-catenin-Wnt/β-catenin axis in colorectal cancer |
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