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Effects of naringin on reversing cisplatin resistance and the Wnt/β-catenin pathway in human ovarian cancer SKOV3/CDDP cells
Objective Ovarian cancer is one of three malignant tumors of the female reproductive system. Our previous studies showed that the traditional Chinese medicine naringin significantly inhibited the proliferation of platinum-resistant ovarian cancer cells in vitro, and that the mechanism may be related...
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Published in: | Journal of international medical research 2020-10, Vol.48 (10), p.300060519887869-300060519887869 |
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creator | Zhu, Hong Zou, Xia Lin, ShiXin Hu, Xin Gao, Jun |
description | Objective
Ovarian cancer is one of three malignant tumors of the female reproductive system. Our previous studies showed that the traditional Chinese medicine naringin significantly inhibited the proliferation of platinum-resistant ovarian cancer cells in vitro, and that the mechanism may be related to the NF-κB pathway.
Methods
The MTT assay was used to detect the sensitivity of SKOV3 and SKOV3/CDDP cells to cisplatin, the effect of different naringin concentrations on the proliferation of SKOV3/CDDP cells, and the reversal of cisplatin resistance in naringin-treated SKOV3/CDDP cells. Western blotting was used to detect β-catenin, c-Myc, and cyclin D1 protein levels in the different cell lines.
Results
MTT results showed that different concentrations of naringin inhibited the proliferation of SKOV3 and SKOV3/CDDP cells, and that the inhibition increased with increasing concentrations and prolonged incubation times. Western blotting revealed that compared with controls (SKOV3/CDDP-0), β-catenin, c-Myc and cyclin D1 proteins levels were significantly decreased in SKOV3/CDDP-C, SKOV3/CDDP-N 20, and SKOV3/CDDP-CN 20 cells, suggesting that naringin inhibited the proliferation of SKOV3/CDDP cells in a concentration and time dependent manner.
Conclusions
Non-cytotoxic naringin reduced the expression of β-catenin, c-Myc, and cyclin D1 in SKOV3/CDDP cells and partially reversed cisplatin resistance in SKOV3/CDDP CN 20 cells. |
doi_str_mv | 10.1177/0300060519887869 |
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Ovarian cancer is one of three malignant tumors of the female reproductive system. Our previous studies showed that the traditional Chinese medicine naringin significantly inhibited the proliferation of platinum-resistant ovarian cancer cells in vitro, and that the mechanism may be related to the NF-κB pathway.
Methods
The MTT assay was used to detect the sensitivity of SKOV3 and SKOV3/CDDP cells to cisplatin, the effect of different naringin concentrations on the proliferation of SKOV3/CDDP cells, and the reversal of cisplatin resistance in naringin-treated SKOV3/CDDP cells. Western blotting was used to detect β-catenin, c-Myc, and cyclin D1 protein levels in the different cell lines.
Results
MTT results showed that different concentrations of naringin inhibited the proliferation of SKOV3 and SKOV3/CDDP cells, and that the inhibition increased with increasing concentrations and prolonged incubation times. Western blotting revealed that compared with controls (SKOV3/CDDP-0), β-catenin, c-Myc and cyclin D1 proteins levels were significantly decreased in SKOV3/CDDP-C, SKOV3/CDDP-N 20, and SKOV3/CDDP-CN 20 cells, suggesting that naringin inhibited the proliferation of SKOV3/CDDP cells in a concentration and time dependent manner.
Conclusions
Non-cytotoxic naringin reduced the expression of β-catenin, c-Myc, and cyclin D1 in SKOV3/CDDP cells and partially reversed cisplatin resistance in SKOV3/CDDP CN 20 cells.</description><identifier>ISSN: 0300-0605</identifier><identifier>EISSN: 1473-2300</identifier><identifier>DOI: 10.1177/0300060519887869</identifier><identifier>PMID: 33086930</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Antineoplastic Agents - pharmacology ; Apoptosis ; Cell growth ; Cell Line, Tumor ; Cell Proliferation ; Chemotherapy ; Cisplatin - pharmacology ; Drug Resistance, Neoplasm ; Female ; Flavanones - pharmacology ; Humans ; Ovarian cancer ; Ovarian Neoplasms - drug therapy ; Pre-Clinical Research Report ; Proteins ; Signal transduction ; Wnt Signaling Pathway</subject><ispartof>Journal of international medical research, 2020-10, Vol.48 (10), p.300060519887869-300060519887869</ispartof><rights>The Author(s) 2019</rights><rights>The Author(s) 2019. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2019 2019 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-e07e572322d5cf9e2123ac7f772a7da3a118119318dbebdb84cb553a3fa8bda13</citedby><cites>FETCH-LOGICAL-c462t-e07e572322d5cf9e2123ac7f772a7da3a118119318dbebdb84cb553a3fa8bda13</cites><orcidid>0000-0002-9145-5363</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588763/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2456224747?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21966,25753,27853,27924,27925,37012,37013,44590,44945,45333,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33086930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Hong</creatorcontrib><creatorcontrib>Zou, Xia</creatorcontrib><creatorcontrib>Lin, ShiXin</creatorcontrib><creatorcontrib>Hu, Xin</creatorcontrib><creatorcontrib>Gao, Jun</creatorcontrib><title>Effects of naringin on reversing cisplatin resistance and the Wnt/β-catenin pathway in human ovarian cancer SKOV3/CDDP cells</title><title>Journal of international medical research</title><addtitle>J Int Med Res</addtitle><description>Objective
Ovarian cancer is one of three malignant tumors of the female reproductive system. Our previous studies showed that the traditional Chinese medicine naringin significantly inhibited the proliferation of platinum-resistant ovarian cancer cells in vitro, and that the mechanism may be related to the NF-κB pathway.
Methods
The MTT assay was used to detect the sensitivity of SKOV3 and SKOV3/CDDP cells to cisplatin, the effect of different naringin concentrations on the proliferation of SKOV3/CDDP cells, and the reversal of cisplatin resistance in naringin-treated SKOV3/CDDP cells. Western blotting was used to detect β-catenin, c-Myc, and cyclin D1 protein levels in the different cell lines.
Results
MTT results showed that different concentrations of naringin inhibited the proliferation of SKOV3 and SKOV3/CDDP cells, and that the inhibition increased with increasing concentrations and prolonged incubation times. Western blotting revealed that compared with controls (SKOV3/CDDP-0), β-catenin, c-Myc and cyclin D1 proteins levels were significantly decreased in SKOV3/CDDP-C, SKOV3/CDDP-N 20, and SKOV3/CDDP-CN 20 cells, suggesting that naringin inhibited the proliferation of SKOV3/CDDP cells in a concentration and time dependent manner.
Conclusions
Non-cytotoxic naringin reduced the expression of β-catenin, c-Myc, and cyclin D1 in SKOV3/CDDP cells and partially reversed cisplatin resistance in SKOV3/CDDP CN 20 cells.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Chemotherapy</subject><subject>Cisplatin - pharmacology</subject><subject>Drug Resistance, Neoplasm</subject><subject>Female</subject><subject>Flavanones - pharmacology</subject><subject>Humans</subject><subject>Ovarian cancer</subject><subject>Ovarian Neoplasms - drug therapy</subject><subject>Pre-Clinical Research Report</subject><subject>Proteins</subject><subject>Signal transduction</subject><subject>Wnt Signaling Pathway</subject><issn>0300-0605</issn><issn>1473-2300</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><recordid>eNp1kU1v1DAQhi0EosvCnROyxIVLWH8ksfeChLYFqlYqEl9Ha-JMdl1lncV2FvXAn-KH8JtwtKUtlTiNPfPMOx6_hDzn7DXnSi2YZIzVrOJLrZWulw_IjJdKFiLnH5LZVC6m-hF5EuMlY6WoK_GYHEnJMi3ZjPw86Tq0KdKhox6C82vn6eBpwD2GmK_UurjrIbkpF11M4C1S8C1NG6TffFr8_lVYSOgzsYO0-QFXNB834xay0j5r5minrkA_nV18lYvV8fFHarHv41PyqIM-4rPrOCdf3p18Xn0ozi_en67enhe2rEUqkCmslJBCtJXtlii4kGBVp5QA1YIEzjXnS8l122DTNrq0TVVJkB3opgUu5-TNQXc3NltsLfoUoDe74LYQrswAzvxb8W5j1sPeqCp_bC2zwKtrgTB8HzEms3VxWgE8DmM0oqxkrXWpJ_TlPfRyGIPP601ULUSpskVzwg6UDUOMAbubx3BmJm_NfW9zy4u7S9w0_DUzA8UBiLDG26n_FfwD7YmtzA</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Zhu, Hong</creator><creator>Zou, Xia</creator><creator>Lin, ShiXin</creator><creator>Hu, Xin</creator><creator>Gao, Jun</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9145-5363</orcidid></search><sort><creationdate>20201001</creationdate><title>Effects of naringin on reversing cisplatin resistance and the Wnt/β-catenin pathway in human ovarian cancer SKOV3/CDDP cells</title><author>Zhu, Hong ; Zou, Xia ; Lin, ShiXin ; Hu, Xin ; Gao, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-e07e572322d5cf9e2123ac7f772a7da3a118119318dbebdb84cb553a3fa8bda13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Apoptosis</topic><topic>Cell growth</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Chemotherapy</topic><topic>Cisplatin - pharmacology</topic><topic>Drug Resistance, Neoplasm</topic><topic>Female</topic><topic>Flavanones - pharmacology</topic><topic>Humans</topic><topic>Ovarian cancer</topic><topic>Ovarian Neoplasms - drug therapy</topic><topic>Pre-Clinical Research Report</topic><topic>Proteins</topic><topic>Signal transduction</topic><topic>Wnt Signaling Pathway</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Hong</creatorcontrib><creatorcontrib>Zou, Xia</creatorcontrib><creatorcontrib>Lin, ShiXin</creatorcontrib><creatorcontrib>Hu, Xin</creatorcontrib><creatorcontrib>Gao, Jun</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of international medical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Hong</au><au>Zou, Xia</au><au>Lin, ShiXin</au><au>Hu, Xin</au><au>Gao, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of naringin on reversing cisplatin resistance and the Wnt/β-catenin pathway in human ovarian cancer SKOV3/CDDP cells</atitle><jtitle>Journal of international medical research</jtitle><addtitle>J Int Med Res</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>48</volume><issue>10</issue><spage>300060519887869</spage><epage>300060519887869</epage><pages>300060519887869-300060519887869</pages><issn>0300-0605</issn><eissn>1473-2300</eissn><abstract>Objective
Ovarian cancer is one of three malignant tumors of the female reproductive system. Our previous studies showed that the traditional Chinese medicine naringin significantly inhibited the proliferation of platinum-resistant ovarian cancer cells in vitro, and that the mechanism may be related to the NF-κB pathway.
Methods
The MTT assay was used to detect the sensitivity of SKOV3 and SKOV3/CDDP cells to cisplatin, the effect of different naringin concentrations on the proliferation of SKOV3/CDDP cells, and the reversal of cisplatin resistance in naringin-treated SKOV3/CDDP cells. Western blotting was used to detect β-catenin, c-Myc, and cyclin D1 protein levels in the different cell lines.
Results
MTT results showed that different concentrations of naringin inhibited the proliferation of SKOV3 and SKOV3/CDDP cells, and that the inhibition increased with increasing concentrations and prolonged incubation times. Western blotting revealed that compared with controls (SKOV3/CDDP-0), β-catenin, c-Myc and cyclin D1 proteins levels were significantly decreased in SKOV3/CDDP-C, SKOV3/CDDP-N 20, and SKOV3/CDDP-CN 20 cells, suggesting that naringin inhibited the proliferation of SKOV3/CDDP cells in a concentration and time dependent manner.
Conclusions
Non-cytotoxic naringin reduced the expression of β-catenin, c-Myc, and cyclin D1 in SKOV3/CDDP cells and partially reversed cisplatin resistance in SKOV3/CDDP CN 20 cells.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>33086930</pmid><doi>10.1177/0300060519887869</doi><orcidid>https://orcid.org/0000-0002-9145-5363</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Apoptosis Cell growth Cell Line, Tumor Cell Proliferation Chemotherapy Cisplatin - pharmacology Drug Resistance, Neoplasm Female Flavanones - pharmacology Humans Ovarian cancer Ovarian Neoplasms - drug therapy Pre-Clinical Research Report Proteins Signal transduction Wnt Signaling Pathway |
title | Effects of naringin on reversing cisplatin resistance and the Wnt/β-catenin pathway in human ovarian cancer SKOV3/CDDP cells |
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