Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis
Iron oxide nanoparticles can induce cell death due to the ferroptosis mechanism, showing a great potential for cancer therapy. Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparti...
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Veröffentlicht in: | ACS applied bio materials 2022-04, Vol.5 (4), p.1692-1699 |
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creator | Tian, Xiangrong Ruan, Li Zhou, Shengwang Wu, Lin Cao, Jin Qi, Xueyong Zhang, Xin Shen, Song |
description | Iron oxide nanoparticles can induce cell death due to the ferroptosis mechanism, showing a great potential for cancer therapy. Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparticles (< ∼5 nm) could accumulate in nucleus and were more efficient in triggering the generation of
OH than larger nanoparticles due to the quicker release of Fe
, thus exhibiting more remarkable cytotoxicity. Nevertheless, 10 nm iron oxide nanoparticles group displayed the best antitumor effect
. We studied the
and intratumoral biodistribution of the nanoparticles and found that the therapeutic effects were related to both the tumoral accumulation and intratumoral distribution of nanoparticles. This work indicates the appropriate size of Fe
O
NPs for cancer treatment and illustrates the possible factors that influence the therapeutic effect, suggesting the great potential of iron oxide in clinical application. |
doi_str_mv | 10.1021/acsabm.2c00068 |
format | Article |
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OH than larger nanoparticles due to the quicker release of Fe
, thus exhibiting more remarkable cytotoxicity. Nevertheless, 10 nm iron oxide nanoparticles group displayed the best antitumor effect
. We studied the
and intratumoral biodistribution of the nanoparticles and found that the therapeutic effects were related to both the tumoral accumulation and intratumoral distribution of nanoparticles. This work indicates the appropriate size of Fe
O
NPs for cancer treatment and illustrates the possible factors that influence the therapeutic effect, suggesting the great potential of iron oxide in clinical application.</description><identifier>ISSN: 2576-6422</identifier><identifier>EISSN: 2576-6422</identifier><identifier>DOI: 10.1021/acsabm.2c00068</identifier><identifier>PMID: 35297253</identifier><language>eng</language><publisher>United States</publisher><subject>Cell Death ; Ferroptosis ; Humans ; Nanoparticles - therapeutic use ; Neoplasms - drug therapy ; Tissue Distribution</subject><ispartof>ACS applied bio materials, 2022-04, Vol.5 (4), p.1692-1699</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1073-29413e41335db3e04ae7a72862ad693a4d121c6cd084bb58438f3f2cd701c33</citedby><cites>FETCH-LOGICAL-c1073-29413e41335db3e04ae7a72862ad693a4d121c6cd084bb58438f3f2cd701c33</cites><orcidid>0000-0002-8762-0397</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2752,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35297253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tian, Xiangrong</creatorcontrib><creatorcontrib>Ruan, Li</creatorcontrib><creatorcontrib>Zhou, Shengwang</creatorcontrib><creatorcontrib>Wu, Lin</creatorcontrib><creatorcontrib>Cao, Jin</creatorcontrib><creatorcontrib>Qi, Xueyong</creatorcontrib><creatorcontrib>Zhang, Xin</creatorcontrib><creatorcontrib>Shen, Song</creatorcontrib><title>Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis</title><title>ACS applied bio materials</title><addtitle>ACS Appl Bio Mater</addtitle><description>Iron oxide nanoparticles can induce cell death due to the ferroptosis mechanism, showing a great potential for cancer therapy. Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparticles (< ∼5 nm) could accumulate in nucleus and were more efficient in triggering the generation of
OH than larger nanoparticles due to the quicker release of Fe
, thus exhibiting more remarkable cytotoxicity. Nevertheless, 10 nm iron oxide nanoparticles group displayed the best antitumor effect
. We studied the
and intratumoral biodistribution of the nanoparticles and found that the therapeutic effects were related to both the tumoral accumulation and intratumoral distribution of nanoparticles. This work indicates the appropriate size of Fe
O
NPs for cancer treatment and illustrates the possible factors that influence the therapeutic effect, suggesting the great potential of iron oxide in clinical application.</description><subject>Cell Death</subject><subject>Ferroptosis</subject><subject>Humans</subject><subject>Nanoparticles - therapeutic use</subject><subject>Neoplasms - drug therapy</subject><subject>Tissue Distribution</subject><issn>2576-6422</issn><issn>2576-6422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkLFOwzAQhi0EolXpyoj8Ain2nZM4YxVRQIro0O7RxXZEUNNEdhjC0xOUghhOd8P3_zp9jN1LsZEC5COZQFW7ASOESPQVW0KcJlGiAK7_3Qu2DuFjQkAIlDq7ZQuMIUshxiUrtn3vu943NDh-aL4c72q-cxz5niv-RueuJz805uQCrzvPczob5_nx3XnqR16NE-yngqELTbhjNzWdgltf9ooddk_H_CUq9s-v-baIjBQpRpApiW4ajG2FTihyKaWgEyCbZEjKSpAmMVZoVVWxVqhrrMHYVEiDuGKbudX4LgTv6nJ6vyU_llKUP17K2Ut58TIFHuZA_1m1zv7hvxbwG7ezXYo</recordid><startdate>20220418</startdate><enddate>20220418</enddate><creator>Tian, Xiangrong</creator><creator>Ruan, Li</creator><creator>Zhou, Shengwang</creator><creator>Wu, Lin</creator><creator>Cao, Jin</creator><creator>Qi, Xueyong</creator><creator>Zhang, Xin</creator><creator>Shen, Song</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-8762-0397</orcidid></search><sort><creationdate>20220418</creationdate><title>Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis</title><author>Tian, Xiangrong ; Ruan, Li ; Zhou, Shengwang ; Wu, Lin ; Cao, Jin ; Qi, Xueyong ; Zhang, Xin ; Shen, Song</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1073-29413e41335db3e04ae7a72862ad693a4d121c6cd084bb58438f3f2cd701c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Cell Death</topic><topic>Ferroptosis</topic><topic>Humans</topic><topic>Nanoparticles - therapeutic use</topic><topic>Neoplasms - drug therapy</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tian, Xiangrong</creatorcontrib><creatorcontrib>Ruan, Li</creatorcontrib><creatorcontrib>Zhou, Shengwang</creatorcontrib><creatorcontrib>Wu, Lin</creatorcontrib><creatorcontrib>Cao, Jin</creatorcontrib><creatorcontrib>Qi, Xueyong</creatorcontrib><creatorcontrib>Zhang, Xin</creatorcontrib><creatorcontrib>Shen, Song</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>ACS applied bio materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tian, Xiangrong</au><au>Ruan, Li</au><au>Zhou, Shengwang</au><au>Wu, Lin</au><au>Cao, Jin</au><au>Qi, Xueyong</au><au>Zhang, Xin</au><au>Shen, Song</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis</atitle><jtitle>ACS applied bio materials</jtitle><addtitle>ACS Appl Bio Mater</addtitle><date>2022-04-18</date><risdate>2022</risdate><volume>5</volume><issue>4</issue><spage>1692</spage><epage>1699</epage><pages>1692-1699</pages><issn>2576-6422</issn><eissn>2576-6422</eissn><abstract>Iron oxide nanoparticles can induce cell death due to the ferroptosis mechanism, showing a great potential for cancer therapy. Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparticles (< ∼5 nm) could accumulate in nucleus and were more efficient in triggering the generation of
OH than larger nanoparticles due to the quicker release of Fe
, thus exhibiting more remarkable cytotoxicity. Nevertheless, 10 nm iron oxide nanoparticles group displayed the best antitumor effect
. We studied the
and intratumoral biodistribution of the nanoparticles and found that the therapeutic effects were related to both the tumoral accumulation and intratumoral distribution of nanoparticles. This work indicates the appropriate size of Fe
O
NPs for cancer treatment and illustrates the possible factors that influence the therapeutic effect, suggesting the great potential of iron oxide in clinical application.</abstract><cop>United States</cop><pmid>35297253</pmid><doi>10.1021/acsabm.2c00068</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8762-0397</orcidid></addata></record> |
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subjects | Cell Death Ferroptosis Humans Nanoparticles - therapeutic use Neoplasms - drug therapy Tissue Distribution |
title | Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis |
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