Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives
Adeno-associated virus (AAV) vectors have gained tremendous attention as in vivo delivery systems in gene therapy for inherited monogenetic diseases. First market approvals, excellent safety data, availability of large-scale production protocols, and the possibility to tailor the vector towards opti...
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Veröffentlicht in: | Cancers 2020-07, Vol.12 (7), p.1889 |
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creator | Hacker, Ulrich T Bentler, Martin Kaniowska, Dorota Morgan, Michael Büning, Hildegard |
description | Adeno-associated virus (AAV) vectors have gained tremendous attention as in vivo delivery systems in gene therapy for inherited monogenetic diseases. First market approvals, excellent safety data, availability of large-scale production protocols, and the possibility to tailor the vector towards optimized and cell-type specific gene transfer offers to move from (ultra) rare to common diseases. Cancer, a major health burden for which novel therapeutic options are urgently needed, represents such a target. We here provide an up-to-date overview of the strategies which are currently developed for the use of AAV vectors in cancer gene therapy and discuss the perspectives for the future translation of these pre-clinical approaches into the clinic. |
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First market approvals, excellent safety data, availability of large-scale production protocols, and the possibility to tailor the vector towards optimized and cell-type specific gene transfer offers to move from (ultra) rare to common diseases. Cancer, a major health burden for which novel therapeutic options are urgently needed, represents such a target. We here provide an up-to-date overview of the strategies which are currently developed for the use of AAV vectors in cancer gene therapy and discuss the perspectives for the future translation of these pre-clinical approaches into the clinic.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers12071889</identifier><identifier>PMID: 32674264</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Cancer ; Clinical trials ; Disease ; Expression vectors ; Gene therapy ; Genetic engineering ; Genomes ; Hemophilia ; Heparan sulfate ; Immunotherapy ; Liver ; Medical research ; Metastasis ; Proteins ; Review ; Tumors ; Vectors (Biology) ; Viruses</subject><ispartof>Cancers, 2020-07, Vol.12 (7), p.1889</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-c8b341fc07b62bcd1c221d9ee202b2ebff7a019fadaadf5c28fa955740c4d3b03</citedby><cites>FETCH-LOGICAL-c421t-c8b341fc07b62bcd1c221d9ee202b2ebff7a019fadaadf5c28fa955740c4d3b03</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/PMC7409174/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409174/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32674264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hacker, Ulrich T</creatorcontrib><creatorcontrib>Bentler, Martin</creatorcontrib><creatorcontrib>Kaniowska, Dorota</creatorcontrib><creatorcontrib>Morgan, Michael</creatorcontrib><creatorcontrib>Büning, Hildegard</creatorcontrib><title>Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Adeno-associated virus (AAV) vectors have gained tremendous attention as in vivo delivery systems in gene therapy for inherited monogenetic diseases. 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We here provide an up-to-date overview of the strategies which are currently developed for the use of AAV vectors in cancer gene therapy and discuss the perspectives for the future translation of these pre-clinical approaches into the clinic.</description><subject>Cancer</subject><subject>Clinical trials</subject><subject>Disease</subject><subject>Expression vectors</subject><subject>Gene therapy</subject><subject>Genetic engineering</subject><subject>Genomes</subject><subject>Hemophilia</subject><subject>Heparan sulfate</subject><subject>Immunotherapy</subject><subject>Liver</subject><subject>Medical research</subject><subject>Metastasis</subject><subject>Proteins</subject><subject>Review</subject><subject>Tumors</subject><subject>Vectors (Biology)</subject><subject>Viruses</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkU1LHjEUhYO0qFjX3ZVAN3YxNV_z1UVhGNQKQgt9-25DJrmpkZlkmsxY_AX-7eatVqzZ5MI95-FcDkJvKfnIeUtOtfIaYqKM1LRp2j10mCdWVFUrXj2bD9BxSjckP85pXdX76ICzqhasEofofhN-q2gS7kfnnVYjvpzmESbwi1pc8DhY3BnwoehSCtqpBQzeurgmfNJ12w94C3oJMWEbIu7_BsIX4AFvriGq-e4T7tcYMw1_z8DsUt7g83VZI-BvOfyc7e4W0hv02qoxwfHjf4R-nJ9t-i_F1deLy767KrRgdCl0M3BBrSb1ULFBG6oZo6YFYIQNDAZra0Voa5VRythSs8aqtixrQbQwfCD8CH1-4M7rMIHROVlUo5yjm1S8k0E5-f_Gu2v5M9zKjGhpLTLg5BEQw68V0iInlzSMo_IQ1iSZYCUhrGRllr5_Ib0Ja_T5vJ1KNFnFd4lOH1Q6hpQi2KcwlMhdz_JFz9nx7vkNT_p_rfI_yVenhg</recordid><startdate>20200714</startdate><enddate>20200714</enddate><creator>Hacker, Ulrich T</creator><creator>Bentler, Martin</creator><creator>Kaniowska, Dorota</creator><creator>Morgan, Michael</creator><creator>Büning, Hildegard</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200714</creationdate><title>Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives</title><author>Hacker, Ulrich T ; Bentler, Martin ; Kaniowska, Dorota ; Morgan, Michael ; Büning, Hildegard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-c8b341fc07b62bcd1c221d9ee202b2ebff7a019fadaadf5c28fa955740c4d3b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cancer</topic><topic>Clinical trials</topic><topic>Disease</topic><topic>Expression vectors</topic><topic>Gene therapy</topic><topic>Genetic engineering</topic><topic>Genomes</topic><topic>Hemophilia</topic><topic>Heparan sulfate</topic><topic>Immunotherapy</topic><topic>Liver</topic><topic>Medical research</topic><topic>Metastasis</topic><topic>Proteins</topic><topic>Review</topic><topic>Tumors</topic><topic>Vectors (Biology)</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hacker, Ulrich T</creatorcontrib><creatorcontrib>Bentler, Martin</creatorcontrib><creatorcontrib>Kaniowska, Dorota</creatorcontrib><creatorcontrib>Morgan, Michael</creatorcontrib><creatorcontrib>Büning, Hildegard</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hacker, Ulrich T</au><au>Bentler, Martin</au><au>Kaniowska, Dorota</au><au>Morgan, Michael</au><au>Büning, Hildegard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2020-07-14</date><risdate>2020</risdate><volume>12</volume><issue>7</issue><spage>1889</spage><pages>1889-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Adeno-associated virus (AAV) vectors have gained tremendous attention as in vivo delivery systems in gene therapy for inherited monogenetic diseases. First market approvals, excellent safety data, availability of large-scale production protocols, and the possibility to tailor the vector towards optimized and cell-type specific gene transfer offers to move from (ultra) rare to common diseases. Cancer, a major health burden for which novel therapeutic options are urgently needed, represents such a target. We here provide an up-to-date overview of the strategies which are currently developed for the use of AAV vectors in cancer gene therapy and discuss the perspectives for the future translation of these pre-clinical approaches into the clinic.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>32674264</pmid><doi>10.3390/cancers12071889</doi><oa>free_for_read</oa></addata></record> |
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subjects | Cancer Clinical trials Disease Expression vectors Gene therapy Genetic engineering Genomes Hemophilia Heparan sulfate Immunotherapy Liver Medical research Metastasis Proteins Review Tumors Vectors (Biology) Viruses |
title | Towards Clinical Implementation of Adeno-Associated Virus (AAV) Vectors for Cancer Gene Therapy: Current Status and Future Perspectives |
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