Mesenchymal stem cells engineered for cancer therapy
Recent pre-clinical and clinical studies have shown that stem cell-based therapies hold tremendous promise for the treatment of human disease. Mesenchymal stem cells (MSC) are emerging as promising anti-cancer agents which have an enormous potential to be utilized to treat a number of different canc...
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Veröffentlicht in: | Advanced drug delivery reviews 2012-06, Vol.64 (8), p.739-748 |
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description | Recent pre-clinical and clinical studies have shown that stem cell-based therapies hold tremendous promise for the treatment of human disease. Mesenchymal stem cells (MSC) are emerging as promising anti-cancer agents which have an enormous potential to be utilized to treat a number of different cancer types. MSC have inherent tumor-trophic migratory properties, which allows them to serve as vehicles for delivering effective, targeted therapy to isolated tumors and metastatic disease. MSC have been readily engineered to express anti-proliferative, pro-apoptotic, anti-angiogenic agents that specifically target different cancer types. Many of these strategies have been validated in a wide range of studies evaluating treatment feasibility or efficacy, as well as establishing methods for real-time monitoring of stem cell migration in vivo for optimal therapy surveillance and accelerated development. This review aims to provide an in depth status of current MSC-based cancer therapies, as well as the prospects for their clinical translation.
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doi_str_mv | 10.1016/j.addr.2011.06.010 |
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[Display omitted]</description><subject>Animals</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - pharmacokinetics</subject><subject>Cancer therapy</subject><subject>Combined Modality Therapy</subject><subject>Delivery vehicles</subject><subject>Diagnostic Imaging</subject><subject>Drug Delivery Systems</subject><subject>Humans</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stromal Cells</subject><subject>Migration</subject><subject>Molecular imaging</subject><subject>Neoplasms - therapy</subject><subject>Targeting</subject><issn>0169-409X</issn><issn>1872-8294</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKAzEUhoMotl5ewIXM0s2MJ5k0TUAEKd6g4kbBXUiTMzZlLjWZFvr2plRFN64O5Hz_n-Qj5IxCQYGKy0VhnAsFA0oLEAVQ2CNDKscsl0zxfTJMkMo5qLcBOYpxAUDZWMAhGTA6TscchoQ_YcTWzjeNqbPYY5NZrOuYYfvuW8SALqu6kFnTWgxZP8dglpsTclCZOuLp1zwmr3e3L5OHfPp8_zi5meaWS9nnxkrF3MwoKsRIYaVcJYHLalyhQ8XKES-pxJkS1HHlmGIIXICgMJNMlsyVx-R617tczRp0Fts-mFovg29M2OjOeP130_q5fu_WuizVSCmZCi6-CkL3scLY68bH7QdNi90qagoll4yPABLKdqgNXYwBq59rKOitbr3QW916q1uD0El3Cp3_fuBP5NtvAq52ACZNa49BR-uTb3Q-oO216_x__Z8z2pEe</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Shah, Khalid</creator><general>Elsevier B.V</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20120601</creationdate><title>Mesenchymal stem cells engineered for cancer therapy</title><author>Shah, Khalid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-ac892dba916659ef9df8048f7fede92354318eb961d49d292e0460610b82832d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - pharmacokinetics</topic><topic>Cancer therapy</topic><topic>Combined Modality Therapy</topic><topic>Delivery vehicles</topic><topic>Diagnostic Imaging</topic><topic>Drug Delivery Systems</topic><topic>Humans</topic><topic>Mesenchymal stem cells</topic><topic>Mesenchymal Stromal Cells</topic><topic>Migration</topic><topic>Molecular imaging</topic><topic>Neoplasms - therapy</topic><topic>Targeting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shah, Khalid</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Advanced drug delivery reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shah, Khalid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal stem cells engineered for cancer therapy</atitle><jtitle>Advanced drug delivery reviews</jtitle><addtitle>Adv Drug Deliv Rev</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>64</volume><issue>8</issue><spage>739</spage><epage>748</epage><pages>739-748</pages><issn>0169-409X</issn><eissn>1872-8294</eissn><abstract>Recent pre-clinical and clinical studies have shown that stem cell-based therapies hold tremendous promise for the treatment of human disease. Mesenchymal stem cells (MSC) are emerging as promising anti-cancer agents which have an enormous potential to be utilized to treat a number of different cancer types. MSC have inherent tumor-trophic migratory properties, which allows them to serve as vehicles for delivering effective, targeted therapy to isolated tumors and metastatic disease. MSC have been readily engineered to express anti-proliferative, pro-apoptotic, anti-angiogenic agents that specifically target different cancer types. Many of these strategies have been validated in a wide range of studies evaluating treatment feasibility or efficacy, as well as establishing methods for real-time monitoring of stem cell migration in vivo for optimal therapy surveillance and accelerated development. This review aims to provide an in depth status of current MSC-based cancer therapies, as well as the prospects for their clinical translation.
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subjects | Animals Antineoplastic Agents - administration & dosage Antineoplastic Agents - pharmacokinetics Cancer therapy Combined Modality Therapy Delivery vehicles Diagnostic Imaging Drug Delivery Systems Humans Mesenchymal stem cells Mesenchymal Stromal Cells Migration Molecular imaging Neoplasms - therapy Targeting |
title | Mesenchymal stem cells engineered for cancer therapy |
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