Nuclear-Targeted Gold Nanoparticles Enhance Cancer Cell Radiosensitization

dc.contributor.author Pratx, Guillem
dc.contributor.author Özçelik, Serdar
dc.contributor.other 04.01. Department of Chemistry
dc.contributor.other 04. Faculty of Science
dc.contributor.other 01. Izmir Institute of Technology
dc.coverage.doi 10.1088/1361-6528/aba02b
dc.date.accessioned 2021-01-24T18:34:42Z
dc.date.available 2021-01-24T18:34:42Z
dc.date.issued 2020
dc.description.abstract Radiation therapy aims to kill or inhibit proliferation of cancer cells while sparing normal cells. To enhance radiosensitization, we developed 40 nm-sized gold nanoparticles targeting the nucleus. We exploited a strategy that combined RGD and NLS peptides respectively targeting cancer cell and the nucleus to initiate cell-death activated by x-ray irradiation. We observed that the modified gold nanoparticles were either translocated in the nuclei or accumulated in the vicinity of the nuclei. We demonstrated that x-ray irradiation at 225 kVp energy reduced cell proliferation by 3.8-fold when the nuclear targeted gold nanoparticles were used. We determined that the radiation dose to have a 10% survival fraction was reduced from 11.0 Gy to 7.1 Gy when 10.0 mu g ml(-1)of the NLS/RGD/PEG-AuNP was incubated with A549 cancer cells. We conclude that the peptide-modified gold nanoparticles targeting the nucleus significantly enhance radiosensitization. en_US
dc.description.sponsorship So thanks to Fulbright Commission for a scholarship partly supporting this work and Melek Ozkan Ucuncu, Ozge Tuncel, Secil Sevim Unluturk, Justin Klein, and Symantak Khan for their support. en_US
dc.identifier.doi 10.1088/1361-6528/aba02b
dc.identifier.doi 10.1088/1361-6528/aba02b en_US
dc.identifier.issn 0957-4484
dc.identifier.issn 1361-6528
dc.identifier.scopus 2-s2.0-85088624767
dc.identifier.uri https://doi.org/10.1088/1361-6528/aba02b
dc.identifier.uri https://hdl.handle.net/11147/10409
dc.language.iso en en_US
dc.publisher IOP Publishing en_US
dc.relation.ispartof Nanotechnology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Gold nanoparticles en_US
dc.subject nuclear targeting en_US
dc.subject NLS peptide modification en_US
dc.subject Radiosensitization en_US
dc.title Nuclear-Targeted Gold Nanoparticles Enhance Cancer Cell Radiosensitization en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Özçelik, Serdar
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Chemistry en_US
gdc.description.issue 41 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.volume 31 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W3037921557
gdc.identifier.pmid 32585647
gdc.identifier.wos WOS:000553444700001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.diamondjournal false
gdc.oaire.impulse 14.0
gdc.oaire.influence 2.8959444E-9
gdc.oaire.isgreen false
gdc.oaire.keywords Cell Nucleus
gdc.oaire.keywords Radiation-Sensitizing Agents
gdc.oaire.keywords Cell Survival
gdc.oaire.keywords Nuclear Localization Signals
gdc.oaire.keywords Metal Nanoparticles
gdc.oaire.keywords Dose-Response Relationship, Radiation
gdc.oaire.keywords A549 Cells
gdc.oaire.keywords Humans
gdc.oaire.keywords Gold
gdc.oaire.keywords Particle Size
gdc.oaire.keywords Oligopeptides
gdc.oaire.keywords Cell Proliferation
gdc.oaire.popularity 1.5797166E-8
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.collaboration International
gdc.openalex.fwci 2.31886449
gdc.openalex.normalizedpercentile 0.89
gdc.openalex.toppercent TOP 10%
gdc.opencitations.count 16
gdc.plumx.crossrefcites 20
gdc.plumx.mendeley 24
gdc.plumx.pubmedcites 12
gdc.plumx.scopuscites 18
gdc.scopus.citedcount 18
gdc.wos.citedcount 22
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