Cu()-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy
Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. Although enormous progress in both photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been made in recent decades, the efficac...
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Veröffentlicht in: | Chemical science (Cambridge) 2023-02, Vol.14 (7), p.188-1819 |
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creator | Jung, Hyo Sung Koo, Seyoung Won, Miae An, Seeun Park, Haebeen Sessler, Jonathan L Han, Jiyou Kim, Jong Seung |
description | Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. Although enormous progress in both photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been made in recent decades, the efficacy of these modalities against CSC remains limited. Here, we report a new generation photosensitizer,
CA9-BPS-Cu(
ii
)
, a system that combines three subunits within a single molecule, namely a copper catalyst for CDT, a boron dipyrromethene photosensitizer for PDT, and acetazolamide for CSC targeting
via
carbonic anhydrase-9 (CA9) binding. A therapeutic effect in MDA-MB-231 cells was observed that is ascribed to elevated oxidative stress mediated by a combined CDT/PDT effect, as well as through copper-catalysed glutathione oxidation. The CSC targeting ability of
CA9-BPS-Cu(
ii
)
was evident from the enhanced affinity of
CA9-BPS-Cu(
ii
)
towards CD133-positive MDA-MB-231 cells where CA9 is overexpressed
vs.
CD133-negative cells. Moreover, the efficacy of
CA9-BPS-Cu(
ii
)
was successfully demonstrated in a xenograft mouse tumour model.
Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. |
doi_str_mv | 10.1039/d2sc03945a |
format | Article |
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CA9-BPS-Cu(
ii
)
, a system that combines three subunits within a single molecule, namely a copper catalyst for CDT, a boron dipyrromethene photosensitizer for PDT, and acetazolamide for CSC targeting
via
carbonic anhydrase-9 (CA9) binding. A therapeutic effect in MDA-MB-231 cells was observed that is ascribed to elevated oxidative stress mediated by a combined CDT/PDT effect, as well as through copper-catalysed glutathione oxidation. The CSC targeting ability of
CA9-BPS-Cu(
ii
)
was evident from the enhanced affinity of
CA9-BPS-Cu(
ii
)
towards CD133-positive MDA-MB-231 cells where CA9 is overexpressed
vs.
CD133-negative cells. Moreover, the efficacy of
CA9-BPS-Cu(
ii
)
was successfully demonstrated in a xenograft mouse tumour model.
Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies.</description><identifier>ISSN: 2041-6520</identifier><identifier>EISSN: 2041-6539</identifier><identifier>DOI: 10.1039/d2sc03945a</identifier><identifier>PMID: 36819853</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Acetazolamide ; Cancer ; Carbonic anhydrase ; Chemistry ; Copper ; Effectiveness ; Glutathione ; Oxidation ; Photodynamic therapy ; Stem cells ; Xenotransplantation</subject><ispartof>Chemical science (Cambridge), 2023-02, Vol.14 (7), p.188-1819</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2023</rights><rights>This journal is © The Royal Society of Chemistry 2023 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-65b87f0079eef09c302f851a07d0681a7d790743386e83f62050a345973dba4e3</citedby><cites>FETCH-LOGICAL-c358t-65b87f0079eef09c302f851a07d0681a7d790743386e83f62050a345973dba4e3</cites><orcidid>0000-0002-9576-1325 ; 0000-0003-2018-8226 ; 0000-0003-3477-1172 ; 0000-0001-5749-3086</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/PMC9930985/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930985/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36819853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Hyo Sung</creatorcontrib><creatorcontrib>Koo, Seyoung</creatorcontrib><creatorcontrib>Won, Miae</creatorcontrib><creatorcontrib>An, Seeun</creatorcontrib><creatorcontrib>Park, Haebeen</creatorcontrib><creatorcontrib>Sessler, Jonathan L</creatorcontrib><creatorcontrib>Han, Jiyou</creatorcontrib><creatorcontrib>Kim, Jong Seung</creatorcontrib><title>Cu()-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy</title><title>Chemical science (Cambridge)</title><addtitle>Chem Sci</addtitle><description>Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. Although enormous progress in both photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been made in recent decades, the efficacy of these modalities against CSC remains limited. Here, we report a new generation photosensitizer,
CA9-BPS-Cu(
ii
)
, a system that combines three subunits within a single molecule, namely a copper catalyst for CDT, a boron dipyrromethene photosensitizer for PDT, and acetazolamide for CSC targeting
via
carbonic anhydrase-9 (CA9) binding. A therapeutic effect in MDA-MB-231 cells was observed that is ascribed to elevated oxidative stress mediated by a combined CDT/PDT effect, as well as through copper-catalysed glutathione oxidation. The CSC targeting ability of
CA9-BPS-Cu(
ii
)
was evident from the enhanced affinity of
CA9-BPS-Cu(
ii
)
towards CD133-positive MDA-MB-231 cells where CA9 is overexpressed
vs.
CD133-negative cells. Moreover, the efficacy of
CA9-BPS-Cu(
ii
)
was successfully demonstrated in a xenograft mouse tumour model.
Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies.</description><subject>Acetazolamide</subject><subject>Cancer</subject><subject>Carbonic anhydrase</subject><subject>Chemistry</subject><subject>Copper</subject><subject>Effectiveness</subject><subject>Glutathione</subject><subject>Oxidation</subject><subject>Photodynamic therapy</subject><subject>Stem cells</subject><subject>Xenotransplantation</subject><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkd1P2zAUxS20CVDhZe-bIu0FkMoc3zi2X5BKykcFEpM2JPZkuc7NGtTGwU4Q3V-PS6Eb88u1dH66OuceQj6l9DiloL6VLNg4M262yC6jWTrMOagPmz-jO2Q_hHsaH0DKmdgmO5DLVEkOu-Sq6A8Oh6c348n3X0k7c50L2IS6q_-gTyrnk2I0uUvcI3p8aj2GgGViTWOjGjpcJBbn86SboTftco98rMw84P7rHJDb87OfxeXw-uZiUoyuhxa47KKnqRQVpUIhVlRZoKySPDVUlDT6MqIUiooMQOYoocoZ5dRAxpWAcmoyhAE5We9t--kCS4tN581ct75eGL_UztT6vdLUM_3bPWqlgK5iD8jB6wLvHnoMnV7UYZXENOj6oJkQCjKZRhMD8vU_9N71vonxVlQeb824jNTRmrLeheCx2phJqV7VpMfsR_FS0yjCX_61v0HfSonA5zXgg92of3uGZ9AIlTw</recordid><startdate>20230215</startdate><enddate>20230215</enddate><creator>Jung, Hyo Sung</creator><creator>Koo, Seyoung</creator><creator>Won, Miae</creator><creator>An, Seeun</creator><creator>Park, Haebeen</creator><creator>Sessler, Jonathan L</creator><creator>Han, Jiyou</creator><creator>Kim, Jong Seung</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9576-1325</orcidid><orcidid>https://orcid.org/0000-0003-2018-8226</orcidid><orcidid>https://orcid.org/0000-0003-3477-1172</orcidid><orcidid>https://orcid.org/0000-0001-5749-3086</orcidid></search><sort><creationdate>20230215</creationdate><title>Cu()-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy</title><author>Jung, Hyo Sung ; Koo, Seyoung ; Won, Miae ; An, Seeun ; Park, Haebeen ; Sessler, Jonathan L ; Han, Jiyou ; Kim, Jong Seung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-65b87f0079eef09c302f851a07d0681a7d790743386e83f62050a345973dba4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetazolamide</topic><topic>Cancer</topic><topic>Carbonic anhydrase</topic><topic>Chemistry</topic><topic>Copper</topic><topic>Effectiveness</topic><topic>Glutathione</topic><topic>Oxidation</topic><topic>Photodynamic therapy</topic><topic>Stem cells</topic><topic>Xenotransplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Hyo Sung</creatorcontrib><creatorcontrib>Koo, Seyoung</creatorcontrib><creatorcontrib>Won, Miae</creatorcontrib><creatorcontrib>An, Seeun</creatorcontrib><creatorcontrib>Park, Haebeen</creatorcontrib><creatorcontrib>Sessler, Jonathan L</creatorcontrib><creatorcontrib>Han, Jiyou</creatorcontrib><creatorcontrib>Kim, Jong Seung</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Hyo Sung</au><au>Koo, Seyoung</au><au>Won, Miae</au><au>An, Seeun</au><au>Park, Haebeen</au><au>Sessler, Jonathan L</au><au>Han, Jiyou</au><au>Kim, Jong Seung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cu()-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy</atitle><jtitle>Chemical science (Cambridge)</jtitle><addtitle>Chem Sci</addtitle><date>2023-02-15</date><risdate>2023</risdate><volume>14</volume><issue>7</issue><spage>188</spage><epage>1819</epage><pages>188-1819</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. Although enormous progress in both photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been made in recent decades, the efficacy of these modalities against CSC remains limited. Here, we report a new generation photosensitizer,
CA9-BPS-Cu(
ii
)
, a system that combines three subunits within a single molecule, namely a copper catalyst for CDT, a boron dipyrromethene photosensitizer for PDT, and acetazolamide for CSC targeting
via
carbonic anhydrase-9 (CA9) binding. A therapeutic effect in MDA-MB-231 cells was observed that is ascribed to elevated oxidative stress mediated by a combined CDT/PDT effect, as well as through copper-catalysed glutathione oxidation. The CSC targeting ability of
CA9-BPS-Cu(
ii
)
was evident from the enhanced affinity of
CA9-BPS-Cu(
ii
)
towards CD133-positive MDA-MB-231 cells where CA9 is overexpressed
vs.
CD133-negative cells. Moreover, the efficacy of
CA9-BPS-Cu(
ii
)
was successfully demonstrated in a xenograft mouse tumour model.
Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>36819853</pmid><doi>10.1039/d2sc03945a</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-9576-1325</orcidid><orcidid>https://orcid.org/0000-0003-2018-8226</orcidid><orcidid>https://orcid.org/0000-0003-3477-1172</orcidid><orcidid>https://orcid.org/0000-0001-5749-3086</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; PubMed Central |
subjects | Acetazolamide Cancer Carbonic anhydrase Chemistry Copper Effectiveness Glutathione Oxidation Photodynamic therapy Stem cells Xenotransplantation |
title | Cu()-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy |
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