Biomimetic Nano‐Cancer Stem Cell Scavenger for Inhibition of Breast Cancer Recurrence and Metastasis after FLASH‐Radiotherapy
Compared to conventional radiotherapy (RT), FLASH‐RT delivers ultra‐high dose radiation, significantly reducing damage to normal tissue while guaranteeing the effect of cancer treatment. However, cancer recurrence and metastasis frequently occur after all RT due to the existence of intractable cance...
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description | Compared to conventional radiotherapy (RT), FLASH‐RT delivers ultra‐high dose radiation, significantly reducing damage to normal tissue while guaranteeing the effect of cancer treatment. However, cancer recurrence and metastasis frequently occur after all RT due to the existence of intractable cancer stem cells (CSCs). To address this, a biomimetic nanoplatform (named TAFL) of tumor‐derived exosome fusion liposomes is designed by co‐loading aggregation‐induced emission photothermal agents, TPE‐BBT, and anti‐cancer drugs, aspirin, aiming to clear CSCs for inhibiting cancer recurrence and metastasis after FLASH‐RT therapy . Aspirin released in TAFL system triggered by laser irradiation can induce apoptosis and DNA damage of 4T1 CSCs, comprehensively downregulate their stemness phenotype, and inhibit their sphericity. Furthermore, the TPE‐BBT mediated mild‐photothermal therapy can alleviate the hypoxic tumor microenvironment, inhibit the DNA repair of CSCs, which further amplifies the effect of aspirin against CSCs, therefore reduces the effective dose of aspirin, making TAFL more biologically safe. In vivo experimental results demonstrated that decreased CSCs population mediated by TAFL system treatment significantly inhibited tumor recurrence and metastasis after FLASH‐RT therapy. In summary, this TAFL system provides a new idea for the future clinical application of FLASH‐RT therapy.
A biomimetic nanoplatform (named TAFL) is designed. TAFL completely down‐regulated stemness phenotype of cancer stem cells (CSCs) and inhibited their pellet‐forming ability. In vivo experimental results demonstrated that the CSCs population decreased notably after TAFL combined with FLASH‐RT therapy radiation treatment under laser irradiation, thus significantly inhibiting tumor recurrence and metastasis post‐FLASH‐RT therapy. |
doi_str_mv | 10.1002/smll.202400666 |
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A biomimetic nanoplatform (named TAFL) is designed. TAFL completely down‐regulated stemness phenotype of cancer stem cells (CSCs) and inhibited their pellet‐forming ability. In vivo experimental results demonstrated that the CSCs population decreased notably after TAFL combined with FLASH‐RT therapy radiation treatment under laser irradiation, thus significantly inhibiting tumor recurrence and metastasis post‐FLASH‐RT therapy.</description><identifier>ISSN: 1613-6810</identifier><identifier>ISSN: 1613-6829</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.202400666</identifier><identifier>PMID: 38368259</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>aggregation‐induced emission ; Aspirin ; Biological effects ; Biomimetics ; cancer recurrence and metastasis ; cancer stem cells ; Cancer therapies ; Chemotherapy ; flash‐radiotherapy ; Laser damage ; Metastasis ; Radiation damage ; Radiation dosage ; Radiation therapy ; Stem cells ; Tumors ; tumor‐derived exosome</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2024-07, Vol.20 (29), p.e2400666-n/a</ispartof><rights>2024 Wiley‐VCH GmbH</rights><rights>2024 Wiley-VCH GmbH.</rights><rights>2024 Wiley‐VCH GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3286-18e8a13396391c7aa01c7f9da34a4c136917b7e851a6c18097631323ed0576a3</cites><orcidid>0000-0002-0293-964X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsmll.202400666$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsmll.202400666$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38368259$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suo, Meng</creatorcontrib><creatorcontrib>Shen, Hanchen</creatorcontrib><creatorcontrib>Lyu, Meng</creatorcontrib><creatorcontrib>Jiang, Yi</creatorcontrib><creatorcontrib>Liao, Xiaoming</creatorcontrib><creatorcontrib>Tang, Wei</creatorcontrib><creatorcontrib>Pan, You</creatorcontrib><creatorcontrib>Zhang, Tianfu</creatorcontrib><creatorcontrib>Ning, Shipeng</creatorcontrib><creatorcontrib>Tang, Ben Zhong</creatorcontrib><title>Biomimetic Nano‐Cancer Stem Cell Scavenger for Inhibition of Breast Cancer Recurrence and Metastasis after FLASH‐Radiotherapy</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>Compared to conventional radiotherapy (RT), FLASH‐RT delivers ultra‐high dose radiation, significantly reducing damage to normal tissue while guaranteeing the effect of cancer treatment. However, cancer recurrence and metastasis frequently occur after all RT due to the existence of intractable cancer stem cells (CSCs). To address this, a biomimetic nanoplatform (named TAFL) of tumor‐derived exosome fusion liposomes is designed by co‐loading aggregation‐induced emission photothermal agents, TPE‐BBT, and anti‐cancer drugs, aspirin, aiming to clear CSCs for inhibiting cancer recurrence and metastasis after FLASH‐RT therapy . Aspirin released in TAFL system triggered by laser irradiation can induce apoptosis and DNA damage of 4T1 CSCs, comprehensively downregulate their stemness phenotype, and inhibit their sphericity. Furthermore, the TPE‐BBT mediated mild‐photothermal therapy can alleviate the hypoxic tumor microenvironment, inhibit the DNA repair of CSCs, which further amplifies the effect of aspirin against CSCs, therefore reduces the effective dose of aspirin, making TAFL more biologically safe. In vivo experimental results demonstrated that decreased CSCs population mediated by TAFL system treatment significantly inhibited tumor recurrence and metastasis after FLASH‐RT therapy. In summary, this TAFL system provides a new idea for the future clinical application of FLASH‐RT therapy.
A biomimetic nanoplatform (named TAFL) is designed. TAFL completely down‐regulated stemness phenotype of cancer stem cells (CSCs) and inhibited their pellet‐forming ability. In vivo experimental results demonstrated that the CSCs population decreased notably after TAFL combined with FLASH‐RT therapy radiation treatment under laser irradiation, thus significantly inhibiting tumor recurrence and metastasis post‐FLASH‐RT therapy.</description><subject>aggregation‐induced emission</subject><subject>Aspirin</subject><subject>Biological effects</subject><subject>Biomimetics</subject><subject>cancer recurrence and metastasis</subject><subject>cancer stem cells</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>flash‐radiotherapy</subject><subject>Laser damage</subject><subject>Metastasis</subject><subject>Radiation damage</subject><subject>Radiation dosage</subject><subject>Radiation therapy</subject><subject>Stem cells</subject><subject>Tumors</subject><subject>tumor‐derived exosome</subject><issn>1613-6810</issn><issn>1613-6829</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhiMEoh9w5YgsceGyi-3JOvaxXdEPKQWp27s160yoqyRe7KRob_AP-I38ElztskhcuMyM_D7z2tZbFG8EnwvO5YfUd91ccllyrpR6VhwLJWCmtDTPD7PgR8VJSg-cg5Bl9bI4Ag0ZWZjj4se5D73vafSOfcIh_Pr-c4mDo8hWI_VsSV3HVg4fafiSz9oQ2fVw79d-9GFgoWXnkTCNbL9zS26KkfLMcGjYDY1ZxOQTw3bM-kV9trrKV9xi48N4TxE321fFixa7RK_3_bS4u_h4t7ya1Z8vr5dn9cyB1GomNGkUAEaBEa5C5Lm2pkEosXQClBHVuiK9EKic0NxUCgRIoIYvKoVwWrzf2W5i-DpRGm3vk8vfw4HClKw0UssSykWZ0Xf_oA9hikN-nAWupQCjATI131EuhpQitXYTfY9xawW3T9nYp2zsIZu88HZvO617ag74nzAyYHbAN9_R9j92dnVT13_NfwPbpZxG</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Suo, Meng</creator><creator>Shen, Hanchen</creator><creator>Lyu, Meng</creator><creator>Jiang, Yi</creator><creator>Liao, Xiaoming</creator><creator>Tang, Wei</creator><creator>Pan, You</creator><creator>Zhang, Tianfu</creator><creator>Ning, Shipeng</creator><creator>Tang, Ben Zhong</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0293-964X</orcidid></search><sort><creationdate>20240701</creationdate><title>Biomimetic Nano‐Cancer Stem Cell Scavenger for Inhibition of Breast Cancer Recurrence and Metastasis after FLASH‐Radiotherapy</title><author>Suo, Meng ; Shen, Hanchen ; Lyu, Meng ; Jiang, Yi ; Liao, Xiaoming ; Tang, Wei ; Pan, You ; Zhang, Tianfu ; Ning, Shipeng ; Tang, Ben Zhong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3286-18e8a13396391c7aa01c7f9da34a4c136917b7e851a6c18097631323ed0576a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>aggregation‐induced emission</topic><topic>Aspirin</topic><topic>Biological effects</topic><topic>Biomimetics</topic><topic>cancer recurrence and metastasis</topic><topic>cancer stem cells</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>flash‐radiotherapy</topic><topic>Laser damage</topic><topic>Metastasis</topic><topic>Radiation damage</topic><topic>Radiation dosage</topic><topic>Radiation therapy</topic><topic>Stem cells</topic><topic>Tumors</topic><topic>tumor‐derived exosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suo, Meng</creatorcontrib><creatorcontrib>Shen, Hanchen</creatorcontrib><creatorcontrib>Lyu, Meng</creatorcontrib><creatorcontrib>Jiang, Yi</creatorcontrib><creatorcontrib>Liao, Xiaoming</creatorcontrib><creatorcontrib>Tang, Wei</creatorcontrib><creatorcontrib>Pan, You</creatorcontrib><creatorcontrib>Zhang, Tianfu</creatorcontrib><creatorcontrib>Ning, Shipeng</creatorcontrib><creatorcontrib>Tang, Ben Zhong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suo, Meng</au><au>Shen, Hanchen</au><au>Lyu, Meng</au><au>Jiang, Yi</au><au>Liao, Xiaoming</au><au>Tang, Wei</au><au>Pan, You</au><au>Zhang, Tianfu</au><au>Ning, Shipeng</au><au>Tang, Ben Zhong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biomimetic Nano‐Cancer Stem Cell Scavenger for Inhibition of Breast Cancer Recurrence and Metastasis after FLASH‐Radiotherapy</atitle><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle><addtitle>Small</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>20</volume><issue>29</issue><spage>e2400666</spage><epage>n/a</epage><pages>e2400666-n/a</pages><issn>1613-6810</issn><issn>1613-6829</issn><eissn>1613-6829</eissn><abstract>Compared to conventional radiotherapy (RT), FLASH‐RT delivers ultra‐high dose radiation, significantly reducing damage to normal tissue while guaranteeing the effect of cancer treatment. However, cancer recurrence and metastasis frequently occur after all RT due to the existence of intractable cancer stem cells (CSCs). To address this, a biomimetic nanoplatform (named TAFL) of tumor‐derived exosome fusion liposomes is designed by co‐loading aggregation‐induced emission photothermal agents, TPE‐BBT, and anti‐cancer drugs, aspirin, aiming to clear CSCs for inhibiting cancer recurrence and metastasis after FLASH‐RT therapy . Aspirin released in TAFL system triggered by laser irradiation can induce apoptosis and DNA damage of 4T1 CSCs, comprehensively downregulate their stemness phenotype, and inhibit their sphericity. Furthermore, the TPE‐BBT mediated mild‐photothermal therapy can alleviate the hypoxic tumor microenvironment, inhibit the DNA repair of CSCs, which further amplifies the effect of aspirin against CSCs, therefore reduces the effective dose of aspirin, making TAFL more biologically safe. In vivo experimental results demonstrated that decreased CSCs population mediated by TAFL system treatment significantly inhibited tumor recurrence and metastasis after FLASH‐RT therapy. In summary, this TAFL system provides a new idea for the future clinical application of FLASH‐RT therapy.
A biomimetic nanoplatform (named TAFL) is designed. TAFL completely down‐regulated stemness phenotype of cancer stem cells (CSCs) and inhibited their pellet‐forming ability. In vivo experimental results demonstrated that the CSCs population decreased notably after TAFL combined with FLASH‐RT therapy radiation treatment under laser irradiation, thus significantly inhibiting tumor recurrence and metastasis post‐FLASH‐RT therapy.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38368259</pmid><doi>10.1002/smll.202400666</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-0293-964X</orcidid></addata></record> |
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subjects | aggregation‐induced emission Aspirin Biological effects Biomimetics cancer recurrence and metastasis cancer stem cells Cancer therapies Chemotherapy flash‐radiotherapy Laser damage Metastasis Radiation damage Radiation dosage Radiation therapy Stem cells Tumors tumor‐derived exosome |
title | Biomimetic Nano‐Cancer Stem Cell Scavenger for Inhibition of Breast Cancer Recurrence and Metastasis after FLASH‐Radiotherapy |
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