Extracellular-vesicles delivered tumor-specific sequential nanocatalysts can be used for MRI-informed nanocatalytic Therapy of hepatocellular carcinoma
Conventional therapeutic strategies for advanced hepatocellular carcinoma (HCC) remains a great challenge, therefore the alternative therapeutic modality for specific and efficient HCC suppression is urgently needed. In this work, HCC-derived extracellular vesicles (EVs) were applied as surface nano...
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description | Conventional therapeutic strategies for advanced hepatocellular carcinoma (HCC) remains a great challenge, therefore the alternative therapeutic modality for specific and efficient HCC suppression is urgently needed.
In this work, HCC-derived extracellular vesicles (EVs) were applied as surface nanocarrier for sequential nanocatalysts GOD-ESIONs@EVs (GE@EVs) of tumor-specific and cascade nanocatalytic therapy against HCC. By enhancing the intracellular endocytosis through arginine-glycine-aspartic acid (RGD)-targeting effect and membrane fusion, sequential nanocatalysts led to more efficient treatment in the HCC tumor region in a shorter period of time.
Through glucose consumption as catalyzed by the loaded glucose oxidase (GOD) to overproduce hydrogen peroxide (H
O
), highly toxic hydroxyl radicals were generated by Fenton-like reaction as catalyzed by ESIONs, which was achieved under the mildly acidic tumor microenvironment, enabling the stimuli of the apoptosis and necrosis of HCC cells. This strategy demonstrated the high active-targeting capability of GE@EVs into HCC, achieving highly efficient tumor suppression both
and
. In addition, the as-synthesized nanoreactor could act as a desirable nanoscale contrast agent for magnetic resonance imaging, which exhibited desirable imaging capability during the sequential nanocatalytic treatment.
This application of surface-engineering EVs not only proves the high-performance catalytic therapeutic modality of GE@EVs for HCC, but also broadens the versatile bio-applications of EVs. |
doi_str_mv | 10.7150/thno.46124 |
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In this work, HCC-derived extracellular vesicles (EVs) were applied as surface nanocarrier for sequential nanocatalysts GOD-ESIONs@EVs (GE@EVs) of tumor-specific and cascade nanocatalytic therapy against HCC. By enhancing the intracellular endocytosis through arginine-glycine-aspartic acid (RGD)-targeting effect and membrane fusion, sequential nanocatalysts led to more efficient treatment in the HCC tumor region in a shorter period of time.
Through glucose consumption as catalyzed by the loaded glucose oxidase (GOD) to overproduce hydrogen peroxide (H
O
), highly toxic hydroxyl radicals were generated by Fenton-like reaction as catalyzed by ESIONs, which was achieved under the mildly acidic tumor microenvironment, enabling the stimuli of the apoptosis and necrosis of HCC cells. This strategy demonstrated the high active-targeting capability of GE@EVs into HCC, achieving highly efficient tumor suppression both
and
. In addition, the as-synthesized nanoreactor could act as a desirable nanoscale contrast agent for magnetic resonance imaging, which exhibited desirable imaging capability during the sequential nanocatalytic treatment.
This application of surface-engineering EVs not only proves the high-performance catalytic therapeutic modality of GE@EVs for HCC, but also broadens the versatile bio-applications of EVs.</description><identifier>ISSN: 1838-7640</identifier><identifier>EISSN: 1838-7640</identifier><identifier>DOI: 10.7150/thno.46124</identifier><identifier>PMID: 33391461</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher Pty Ltd</publisher><subject>Cancer therapies ; Chemotherapy ; Cytotoxicity ; Enzymes ; Extracellular vesicles ; Glucose ; Ligands ; Liver cancer ; Magnetic resonance imaging ; Nanoparticles ; Particle size ; Peptides ; Proteins ; Research Paper ; Spectrum analysis ; Tumors</subject><ispartof>Theranostics, 2021-01, Vol.11 (1), p.64-78</ispartof><rights>The author(s).</rights><rights>2021. This work is published under https://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><rights>The author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-519cafc13bb81280b77e4f3398159d0c5278a5f08b66d5d930bb12fc7698fc863</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681081/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7681081/$$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/33391461$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Han</creatorcontrib><creatorcontrib>Xing, Hao</creatorcontrib><creatorcontrib>Wu, Meng-Chao</creatorcontrib><creatorcontrib>Shen, Feng</creatorcontrib><creatorcontrib>Chen, Yu</creatorcontrib><creatorcontrib>Yang, Tian</creatorcontrib><title>Extracellular-vesicles delivered tumor-specific sequential nanocatalysts can be used for MRI-informed nanocatalytic Therapy of hepatocellular carcinoma</title><title>Theranostics</title><addtitle>Theranostics</addtitle><description>Conventional therapeutic strategies for advanced hepatocellular carcinoma (HCC) remains a great challenge, therefore the alternative therapeutic modality for specific and efficient HCC suppression is urgently needed.
In this work, HCC-derived extracellular vesicles (EVs) were applied as surface nanocarrier for sequential nanocatalysts GOD-ESIONs@EVs (GE@EVs) of tumor-specific and cascade nanocatalytic therapy against HCC. By enhancing the intracellular endocytosis through arginine-glycine-aspartic acid (RGD)-targeting effect and membrane fusion, sequential nanocatalysts led to more efficient treatment in the HCC tumor region in a shorter period of time.
Through glucose consumption as catalyzed by the loaded glucose oxidase (GOD) to overproduce hydrogen peroxide (H
O
), highly toxic hydroxyl radicals were generated by Fenton-like reaction as catalyzed by ESIONs, which was achieved under the mildly acidic tumor microenvironment, enabling the stimuli of the apoptosis and necrosis of HCC cells. This strategy demonstrated the high active-targeting capability of GE@EVs into HCC, achieving highly efficient tumor suppression both
and
. In addition, the as-synthesized nanoreactor could act as a desirable nanoscale contrast agent for magnetic resonance imaging, which exhibited desirable imaging capability during the sequential nanocatalytic treatment.
This application of surface-engineering EVs not only proves the high-performance catalytic therapeutic modality of GE@EVs for HCC, but also broadens the versatile bio-applications of EVs.</description><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Cytotoxicity</subject><subject>Enzymes</subject><subject>Extracellular vesicles</subject><subject>Glucose</subject><subject>Ligands</subject><subject>Liver cancer</subject><subject>Magnetic resonance imaging</subject><subject>Nanoparticles</subject><subject>Particle size</subject><subject>Peptides</subject><subject>Proteins</subject><subject>Research Paper</subject><subject>Spectrum analysis</subject><subject>Tumors</subject><issn>1838-7640</issn><issn>1838-7640</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpVUU1LAzEQDaKoVC_-AAl4E7Ymu9nd7EUQqR-gCFLPIZtNbEqarEm22F_i3zW1WjWXGWbevHmTB8AJRuMal-gizqwbkwrnZAccYlrQrK4I2v2TH4DjEOYoPYLyBjf74KAoiganoUPwMXmPngtpzGC4z5YyaGFkgJ00eim97GAcFs5noZdCKy1gkG-DtFFzAy23TvDIzSrEAAW3sJVwCGlGOQ8fn-8zbVO2SIVfaEwc05n0vF9Bp-BM9jy6n_2JxAtt3YIfgT3FTZDH33EEXm4m0-u77OHp9v766iETBFUxK3EjuBK4aFuKc4raupZEpesoLpsOiTKvKS8Vom1VdWXXFKhtca5EXTVUCVoVI3C54e2HNgkV6TTPDeu9XnC_Yo5r9r9j9Yy9uiWrK4oRxYng7JvAu_QzIbK5G7xNmlleNjQnhOR1Qp1vUMK7ELxU2w0YsbWPbO0j-_IxgU__atpCf1wrPgH2D54K</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Wu, Han</creator><creator>Xing, Hao</creator><creator>Wu, Meng-Chao</creator><creator>Shen, Feng</creator><creator>Chen, Yu</creator><creator>Yang, Tian</creator><general>Ivyspring International Publisher Pty Ltd</general><general>Ivyspring International Publisher</general><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>5PM</scope></search><sort><creationdate>20210101</creationdate><title>Extracellular-vesicles delivered tumor-specific sequential nanocatalysts can be used for MRI-informed nanocatalytic Therapy of hepatocellular carcinoma</title><author>Wu, Han ; Xing, Hao ; Wu, Meng-Chao ; Shen, Feng ; Chen, Yu ; Yang, Tian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-519cafc13bb81280b77e4f3398159d0c5278a5f08b66d5d930bb12fc7698fc863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Cytotoxicity</topic><topic>Enzymes</topic><topic>Extracellular vesicles</topic><topic>Glucose</topic><topic>Ligands</topic><topic>Liver cancer</topic><topic>Magnetic resonance imaging</topic><topic>Nanoparticles</topic><topic>Particle size</topic><topic>Peptides</topic><topic>Proteins</topic><topic>Research Paper</topic><topic>Spectrum analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Han</creatorcontrib><creatorcontrib>Xing, Hao</creatorcontrib><creatorcontrib>Wu, Meng-Chao</creatorcontrib><creatorcontrib>Shen, Feng</creatorcontrib><creatorcontrib>Chen, Yu</creatorcontrib><creatorcontrib>Yang, Tian</creatorcontrib><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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>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>PubMed Central (Full Participant titles)</collection><jtitle>Theranostics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Han</au><au>Xing, Hao</au><au>Wu, Meng-Chao</au><au>Shen, Feng</au><au>Chen, Yu</au><au>Yang, Tian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extracellular-vesicles delivered tumor-specific sequential nanocatalysts can be used for MRI-informed nanocatalytic Therapy of hepatocellular carcinoma</atitle><jtitle>Theranostics</jtitle><addtitle>Theranostics</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>11</volume><issue>1</issue><spage>64</spage><epage>78</epage><pages>64-78</pages><issn>1838-7640</issn><eissn>1838-7640</eissn><abstract>Conventional therapeutic strategies for advanced hepatocellular carcinoma (HCC) remains a great challenge, therefore the alternative therapeutic modality for specific and efficient HCC suppression is urgently needed.
In this work, HCC-derived extracellular vesicles (EVs) were applied as surface nanocarrier for sequential nanocatalysts GOD-ESIONs@EVs (GE@EVs) of tumor-specific and cascade nanocatalytic therapy against HCC. By enhancing the intracellular endocytosis through arginine-glycine-aspartic acid (RGD)-targeting effect and membrane fusion, sequential nanocatalysts led to more efficient treatment in the HCC tumor region in a shorter period of time.
Through glucose consumption as catalyzed by the loaded glucose oxidase (GOD) to overproduce hydrogen peroxide (H
O
), highly toxic hydroxyl radicals were generated by Fenton-like reaction as catalyzed by ESIONs, which was achieved under the mildly acidic tumor microenvironment, enabling the stimuli of the apoptosis and necrosis of HCC cells. This strategy demonstrated the high active-targeting capability of GE@EVs into HCC, achieving highly efficient tumor suppression both
and
. In addition, the as-synthesized nanoreactor could act as a desirable nanoscale contrast agent for magnetic resonance imaging, which exhibited desirable imaging capability during the sequential nanocatalytic treatment.
This application of surface-engineering EVs not only proves the high-performance catalytic therapeutic modality of GE@EVs for HCC, but also broadens the versatile bio-applications of EVs.</abstract><cop>Australia</cop><pub>Ivyspring International Publisher Pty Ltd</pub><pmid>33391461</pmid><doi>10.7150/thno.46124</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cancer therapies Chemotherapy Cytotoxicity Enzymes Extracellular vesicles Glucose Ligands Liver cancer Magnetic resonance imaging Nanoparticles Particle size Peptides Proteins Research Paper Spectrum analysis Tumors |
title | Extracellular-vesicles delivered tumor-specific sequential nanocatalysts can be used for MRI-informed nanocatalytic Therapy of hepatocellular carcinoma |
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