Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells
Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization...
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description | Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis. |
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The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-22250-8</identifier><identifier>PMID: 29500444</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/1 ; 13/106 ; 13/109 ; 13/89 ; 13/95 ; 14 ; 14/19 ; 631/154/152 ; 631/67/1347 ; Antidiabetics ; Breast cancer ; Caveolin ; Caveolin-1 ; Cytotoxicity ; Diabetes mellitus ; Drug efficacy ; Endocytosis ; ErbB-2 protein ; Humanities and Social Sciences ; Internalization ; Metastases ; Metformin ; Monoclonal antibodies ; multidisciplinary ; Science ; Science (multidisciplinary) ; Signal transduction ; Targeted cancer therapy ; Trastuzumab</subject><ispartof>Scientific reports, 2018-03, Vol.8 (1), p.3930-9, Article 3930</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-5ce977d46a32cd10f2ab6f78f68fb8d92e7327afd1bb17305d4772658ff490c43</citedby><cites>FETCH-LOGICAL-c474t-5ce977d46a32cd10f2ab6f78f68fb8d92e7327afd1bb17305d4772658ff490c43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834501/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834501/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,41118,42187,51574,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29500444$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chung, Yuan-Chiang</creatorcontrib><creatorcontrib>Chang, Ching-Ming</creatorcontrib><creatorcontrib>Wei, Wan-Chen</creatorcontrib><creatorcontrib>Chang, Ting-Wei</creatorcontrib><creatorcontrib>Chang, King-Jen</creatorcontrib><creatorcontrib>Chao, Wei-Ting</creatorcontrib><title>Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis.</description><subject>13/1</subject><subject>13/106</subject><subject>13/109</subject><subject>13/89</subject><subject>13/95</subject><subject>14</subject><subject>14/19</subject><subject>631/154/152</subject><subject>631/67/1347</subject><subject>Antidiabetics</subject><subject>Breast cancer</subject><subject>Caveolin</subject><subject>Caveolin-1</subject><subject>Cytotoxicity</subject><subject>Diabetes mellitus</subject><subject>Drug efficacy</subject><subject>Endocytosis</subject><subject>ErbB-2 protein</subject><subject>Humanities and Social Sciences</subject><subject>Internalization</subject><subject>Metastases</subject><subject>Metformin</subject><subject>Monoclonal antibodies</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Signal transduction</subject><subject>Targeted cancer therapy</subject><subject>Trastuzumab</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1vFSEUhidGY5vaP-DCkLhxg_J5gY2JqZ9JGzd15YIwcLjSzMAVZhr77-V6a60uZAPhPOc9vLzD8JSSl5Rw_aoJKo3GhGrMGJME6wfDMSNCYsYZe3jvfDSctnZF-pLMCGoeD0fMSEKEEMfD1wtYYqlzyjjlsHoIyLtrKFO_oAh-7Cq0lkpGu1rmskBDl_jtBUWhrlsEMSbv_A1KGY0VXFt6c_ZQkYdpak-GR9FNDU5v95Phy_t3l2cf8fnnD5_O3pxjL5RYsPRglApi4zjzgZLI3LiJSseNjqMOhoHiTLkY6DhSxYkMQim2kTpGYYgX_GR4fdDdreMMwUNeqpvsrqbZ1RtbXLJ_V3L6Zrfl2krNhSS0C7y4Fajl-wptsXNqewsuQ1mbZaR_ueJC7NHn_6BXZa252-sUMVppZlin2IHytbRWId49hhK7j88e4rM9PvsrPqt707P7Nu5afofVAX4AWi_lLdQ_s_8j-xMDOKWw</recordid><startdate>20180302</startdate><enddate>20180302</enddate><creator>Chung, Yuan-Chiang</creator><creator>Chang, Ching-Ming</creator><creator>Wei, Wan-Chen</creator><creator>Chang, Ting-Wei</creator><creator>Chang, King-Jen</creator><creator>Chao, Wei-Ting</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180302</creationdate><title>Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells</title><author>Chung, Yuan-Chiang ; 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The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29500444</pmid><doi>10.1038/s41598-018-22250-8</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/1 13/106 13/109 13/89 13/95 14 14/19 631/154/152 631/67/1347 Antidiabetics Breast cancer Caveolin Caveolin-1 Cytotoxicity Diabetes mellitus Drug efficacy Endocytosis ErbB-2 protein Humanities and Social Sciences Internalization Metastases Metformin Monoclonal antibodies multidisciplinary Science Science (multidisciplinary) Signal transduction Targeted cancer therapy Trastuzumab |
title | Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells |
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