Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer
Tumor stroma plays an important role in the occurrence, development, and metastasis of colorectal cancer (CRC). The dense collagenous stroma forms a physical barrier for antitumor drugs and sustains a highly tumor immunosuppressive microenvironment. To address this issue, a spatiotemporal combinatio...
Gespeichert in:
Veröffentlicht in: | Biomaterials science 2022-09, Vol.1 (19), p.5596-567 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 567 |
---|---|
container_issue | 19 |
container_start_page | 5596 |
container_title | Biomaterials science |
container_volume | 1 |
creator | Ni, Weidong Wu, Jiayan Feng, Yuanji Hu, Yingying Liu, Haiyan Chen, Jie Chen, Fangfang Tian, Huayu |
description | Tumor stroma plays an important role in the occurrence, development, and metastasis of colorectal cancer (CRC). The dense collagenous stroma forms a physical barrier for antitumor drugs and sustains a highly tumor immunosuppressive microenvironment. To address this issue, a spatiotemporal combination of antitumor stroma and nanoscale functional materials was used as an antitumor strategy for reprogramming the tumor immune microenvironment. In this combination, metformin hydrochloride (MET) was intraperitoneally injected to disrupt the dense tumor stroma for promoting drug delivery and remodeling the tumor immune microenvironment. Subsequently, intravenously injected multifunctional drug-delivery materials (MIL-100/mitoxantrone/hyaluronic acid nanoparticles, MMH NPs) were visualized by double imaging (photoacoustic (PA) and fluorescence imaging) and generated a robust immune response
via
immunogenic cell death (ICD). More importantly, the combination treatment also acted synergistically with the anti-OX40 agonist antibody (αOX40), which enhanced the treatment of orthotopic CRC. In summary, the combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for CRC therapy.
The combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for colorectal cancer therapy. |
doi_str_mv | 10.1039/d2bm00988a |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_d2bm00988a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2718179763</sourcerecordid><originalsourceid>FETCH-LOGICAL-c314t-f44cb4aad9535e2ce728deb3471ff4293fb3dd9f1445c2d768d41f37d0c98dca3</originalsourceid><addsrcrecordid>eNpdkU1LAzEQhoMoWGov3oWAFxGqySZtkmOtn9DiRa8u2XzYLZukJlmh_95opYJzmTk8vMw8A8ApRlcYEXGtq8YhJDiXB2BQIcrGlFNxuJ8JOgajlNaoFGMCTfEAvC1NtiG61sNoNjG8R-kSzL0LEbpWxWD8ZxuDd8ZnKL2GTQgpJ6hWxoXWud6HvDJRbrawRKjQhWhUlh1U0isTT8CRlV0yo98-BK_3dy_zx_Hi-eFpPluMFcE0jy2lqqFSajEhE1MpwyquTUMow9bSShDbEK2FxZROVKXZlGuKLWEaKcG1kmQILna55YSP3qRcuzYp03XSm9CnumJFEKeU8IKe_0PXoY--bFcozDETbEoKdbmjioKUorH1JrZOxm2NUf1tu76tbpY_tmcFPtvBMak99_cN8gVZ_X39</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2718179763</pqid></control><display><type>article</type><title>Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer</title><source>Royal Society Of Chemistry Journals 2008-</source><creator>Ni, Weidong ; Wu, Jiayan ; Feng, Yuanji ; Hu, Yingying ; Liu, Haiyan ; Chen, Jie ; Chen, Fangfang ; Tian, Huayu</creator><creatorcontrib>Ni, Weidong ; Wu, Jiayan ; Feng, Yuanji ; Hu, Yingying ; Liu, Haiyan ; Chen, Jie ; Chen, Fangfang ; Tian, Huayu</creatorcontrib><description>Tumor stroma plays an important role in the occurrence, development, and metastasis of colorectal cancer (CRC). The dense collagenous stroma forms a physical barrier for antitumor drugs and sustains a highly tumor immunosuppressive microenvironment. To address this issue, a spatiotemporal combination of antitumor stroma and nanoscale functional materials was used as an antitumor strategy for reprogramming the tumor immune microenvironment. In this combination, metformin hydrochloride (MET) was intraperitoneally injected to disrupt the dense tumor stroma for promoting drug delivery and remodeling the tumor immune microenvironment. Subsequently, intravenously injected multifunctional drug-delivery materials (MIL-100/mitoxantrone/hyaluronic acid nanoparticles, MMH NPs) were visualized by double imaging (photoacoustic (PA) and fluorescence imaging) and generated a robust immune response
via
immunogenic cell death (ICD). More importantly, the combination treatment also acted synergistically with the anti-OX40 agonist antibody (αOX40), which enhanced the treatment of orthotopic CRC. In summary, the combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for CRC therapy.
The combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for colorectal cancer therapy.</description><identifier>ISSN: 2047-4830</identifier><identifier>EISSN: 2047-4849</identifier><identifier>DOI: 10.1039/d2bm00988a</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Antibodies ; Barriers ; Cancer ; Cell death ; Colorectal cancer ; Functional materials ; Hyaluronic acid ; Immune system ; Metformin ; Nanoparticles</subject><ispartof>Biomaterials science, 2022-09, Vol.1 (19), p.5596-567</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-f44cb4aad9535e2ce728deb3471ff4293fb3dd9f1445c2d768d41f37d0c98dca3</citedby><cites>FETCH-LOGICAL-c314t-f44cb4aad9535e2ce728deb3471ff4293fb3dd9f1445c2d768d41f37d0c98dca3</cites><orcidid>0000-0002-2482-3744 ; 0000-0003-1945-0047</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Ni, Weidong</creatorcontrib><creatorcontrib>Wu, Jiayan</creatorcontrib><creatorcontrib>Feng, Yuanji</creatorcontrib><creatorcontrib>Hu, Yingying</creatorcontrib><creatorcontrib>Liu, Haiyan</creatorcontrib><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Chen, Fangfang</creatorcontrib><creatorcontrib>Tian, Huayu</creatorcontrib><title>Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer</title><title>Biomaterials science</title><description>Tumor stroma plays an important role in the occurrence, development, and metastasis of colorectal cancer (CRC). The dense collagenous stroma forms a physical barrier for antitumor drugs and sustains a highly tumor immunosuppressive microenvironment. To address this issue, a spatiotemporal combination of antitumor stroma and nanoscale functional materials was used as an antitumor strategy for reprogramming the tumor immune microenvironment. In this combination, metformin hydrochloride (MET) was intraperitoneally injected to disrupt the dense tumor stroma for promoting drug delivery and remodeling the tumor immune microenvironment. Subsequently, intravenously injected multifunctional drug-delivery materials (MIL-100/mitoxantrone/hyaluronic acid nanoparticles, MMH NPs) were visualized by double imaging (photoacoustic (PA) and fluorescence imaging) and generated a robust immune response
via
immunogenic cell death (ICD). More importantly, the combination treatment also acted synergistically with the anti-OX40 agonist antibody (αOX40), which enhanced the treatment of orthotopic CRC. In summary, the combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for CRC therapy.
The combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for colorectal cancer therapy.</description><subject>Antibodies</subject><subject>Barriers</subject><subject>Cancer</subject><subject>Cell death</subject><subject>Colorectal cancer</subject><subject>Functional materials</subject><subject>Hyaluronic acid</subject><subject>Immune system</subject><subject>Metformin</subject><subject>Nanoparticles</subject><issn>2047-4830</issn><issn>2047-4849</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkU1LAzEQhoMoWGov3oWAFxGqySZtkmOtn9DiRa8u2XzYLZukJlmh_95opYJzmTk8vMw8A8ApRlcYEXGtq8YhJDiXB2BQIcrGlFNxuJ8JOgajlNaoFGMCTfEAvC1NtiG61sNoNjG8R-kSzL0LEbpWxWD8ZxuDd8ZnKL2GTQgpJ6hWxoXWud6HvDJRbrawRKjQhWhUlh1U0isTT8CRlV0yo98-BK_3dy_zx_Hi-eFpPluMFcE0jy2lqqFSajEhE1MpwyquTUMow9bSShDbEK2FxZROVKXZlGuKLWEaKcG1kmQILna55YSP3qRcuzYp03XSm9CnumJFEKeU8IKe_0PXoY--bFcozDETbEoKdbmjioKUorH1JrZOxm2NUf1tu76tbpY_tmcFPtvBMak99_cN8gVZ_X39</recordid><startdate>20220927</startdate><enddate>20220927</enddate><creator>Ni, Weidong</creator><creator>Wu, Jiayan</creator><creator>Feng, Yuanji</creator><creator>Hu, Yingying</creator><creator>Liu, Haiyan</creator><creator>Chen, Jie</creator><creator>Chen, Fangfang</creator><creator>Tian, Huayu</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2482-3744</orcidid><orcidid>https://orcid.org/0000-0003-1945-0047</orcidid></search><sort><creationdate>20220927</creationdate><title>Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer</title><author>Ni, Weidong ; Wu, Jiayan ; Feng, Yuanji ; Hu, Yingying ; Liu, Haiyan ; Chen, Jie ; Chen, Fangfang ; Tian, Huayu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-f44cb4aad9535e2ce728deb3471ff4293fb3dd9f1445c2d768d41f37d0c98dca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies</topic><topic>Barriers</topic><topic>Cancer</topic><topic>Cell death</topic><topic>Colorectal cancer</topic><topic>Functional materials</topic><topic>Hyaluronic acid</topic><topic>Immune system</topic><topic>Metformin</topic><topic>Nanoparticles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ni, Weidong</creatorcontrib><creatorcontrib>Wu, Jiayan</creatorcontrib><creatorcontrib>Feng, Yuanji</creatorcontrib><creatorcontrib>Hu, Yingying</creatorcontrib><creatorcontrib>Liu, Haiyan</creatorcontrib><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Chen, Fangfang</creatorcontrib><creatorcontrib>Tian, Huayu</creatorcontrib><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><jtitle>Biomaterials science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ni, Weidong</au><au>Wu, Jiayan</au><au>Feng, Yuanji</au><au>Hu, Yingying</au><au>Liu, Haiyan</au><au>Chen, Jie</au><au>Chen, Fangfang</au><au>Tian, Huayu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer</atitle><jtitle>Biomaterials science</jtitle><date>2022-09-27</date><risdate>2022</risdate><volume>1</volume><issue>19</issue><spage>5596</spage><epage>567</epage><pages>5596-567</pages><issn>2047-4830</issn><eissn>2047-4849</eissn><abstract>Tumor stroma plays an important role in the occurrence, development, and metastasis of colorectal cancer (CRC). The dense collagenous stroma forms a physical barrier for antitumor drugs and sustains a highly tumor immunosuppressive microenvironment. To address this issue, a spatiotemporal combination of antitumor stroma and nanoscale functional materials was used as an antitumor strategy for reprogramming the tumor immune microenvironment. In this combination, metformin hydrochloride (MET) was intraperitoneally injected to disrupt the dense tumor stroma for promoting drug delivery and remodeling the tumor immune microenvironment. Subsequently, intravenously injected multifunctional drug-delivery materials (MIL-100/mitoxantrone/hyaluronic acid nanoparticles, MMH NPs) were visualized by double imaging (photoacoustic (PA) and fluorescence imaging) and generated a robust immune response
via
immunogenic cell death (ICD). More importantly, the combination treatment also acted synergistically with the anti-OX40 agonist antibody (αOX40), which enhanced the treatment of orthotopic CRC. In summary, the combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for CRC therapy.
The combination strategy of MET/MMH NPs/αOX40 provides a novel and effective clinical option for colorectal cancer therapy.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2bm00988a</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-2482-3744</orcidid><orcidid>https://orcid.org/0000-0003-1945-0047</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2047-4830 |
ispartof | Biomaterials science, 2022-09, Vol.1 (19), p.5596-567 |
issn | 2047-4830 2047-4849 |
language | eng |
recordid | cdi_rsc_primary_d2bm00988a |
source | Royal Society Of Chemistry Journals 2008- |
subjects | Antibodies Barriers Cancer Cell death Colorectal cancer Functional materials Hyaluronic acid Immune system Metformin Nanoparticles |
title | Metformin reprograms tumor microenvironment and boosts chemoimmunotherapy in colorectal cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T18%3A10%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_rsc_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Metformin%20reprograms%20tumor%20microenvironment%20and%20boosts%20chemoimmunotherapy%20in%20colorectal%20cancer&rft.jtitle=Biomaterials%20science&rft.au=Ni,%20Weidong&rft.date=2022-09-27&rft.volume=1&rft.issue=19&rft.spage=5596&rft.epage=567&rft.pages=5596-567&rft.issn=2047-4830&rft.eissn=2047-4849&rft_id=info:doi/10.1039/d2bm00988a&rft_dat=%3Cproquest_rsc_p%3E2718179763%3C/proquest_rsc_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2718179763&rft_id=info:pmid/&rfr_iscdi=true |