Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy
High atomic number (Z) materials such as gold preferentially absorb kilovoltage x-rays compared to soft tissue and may be used to achieve local dose enhancement in tumours during treatment with ionizing radiation. Gold nanoparticles have been demonstrated as radiation dose enhancing agents in vivo a...
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Veröffentlicht in: | Nanotechnology 2010-07, Vol.21 (29), p.295101-295101 |
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creator | Butterworth, K T Coulter, J A Jain, S Forker, J McMahon, S J Schettino, G Prise, K M Currell, F J Hirst, D G |
description | High atomic number (Z) materials such as gold preferentially absorb kilovoltage x-rays compared to soft tissue and may be used to achieve local dose enhancement in tumours during treatment with ionizing radiation. Gold nanoparticles have been demonstrated as radiation dose enhancing agents in vivo and in vitro. In the present study, we used multiple endpoints to characterize the cellular cytotoxic response of a range of cell lines to 1.9 nm gold particles and measured dose modifying effects following transient exposure at low concentrations. Gold nanoparticles caused significant levels of cell type specific cytotoxicity, apoptosis and increased oxidative stress. When used as dose modifying agents, dose enhancement factors varied between the cell lines investigated with the highest enhancement being 1.9 in AGO-1522B cells at a nanoparticle concentration of 100 microg ml(-1). This study shows exposure to 1.9 nm gold particles to induce a range of cell line specific responses including decreased clonogenic survival, increased apoptosis and induction of DNA damage which may be mediated through the production of reactive oxygen species. This is the first study involving 1.9 nm nanometre sized particles to report multiple cellular responses which impact on the radiation dose modifying effect. The findings highlight the need for extensive characterization of responses to gold nanoparticles when assessing dose enhancing potential in cancer therapy. |
doi_str_mv | 10.1088/0957-4484/21/29/295101 |
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Gold nanoparticles have been demonstrated as radiation dose enhancing agents in vivo and in vitro. In the present study, we used multiple endpoints to characterize the cellular cytotoxic response of a range of cell lines to 1.9 nm gold particles and measured dose modifying effects following transient exposure at low concentrations. Gold nanoparticles caused significant levels of cell type specific cytotoxicity, apoptosis and increased oxidative stress. When used as dose modifying agents, dose enhancement factors varied between the cell lines investigated with the highest enhancement being 1.9 in AGO-1522B cells at a nanoparticle concentration of 100 microg ml(-1). This study shows exposure to 1.9 nm gold particles to induce a range of cell line specific responses including decreased clonogenic survival, increased apoptosis and induction of DNA damage which may be mediated through the production of reactive oxygen species. This is the first study involving 1.9 nm nanometre sized particles to report multiple cellular responses which impact on the radiation dose modifying effect. The findings highlight the need for extensive characterization of responses to gold nanoparticles when assessing dose enhancing potential in cancer therapy.</description><identifier>ISSN: 0957-4484</identifier><identifier>EISSN: 1361-6528</identifier><identifier>DOI: 10.1088/0957-4484/21/29/295101</identifier><identifier>PMID: 20601762</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>Apoptosis - drug effects ; Apoptosis - radiation effects ; Cell Growth Processes - drug effects ; Cell Growth Processes - radiation effects ; Cell Line, Tumor ; Cell Survival - drug effects ; Cell Survival - radiation effects ; DNA Breaks, Double-Stranded ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Flow Cytometry ; Gold - administration & dosage ; Gold - pharmacokinetics ; Gold - pharmacology ; Humans ; Metal Nanoparticles - chemistry ; Metal Nanoparticles - therapeutic use ; Nonlinear Dynamics ; Oxidation-Reduction ; Oxidative Stress - drug effects ; Oxidative Stress - radiation effects ; Radiation-Sensitizing Agents - administration & dosage ; Radiation-Sensitizing Agents - chemistry ; Radiation-Sensitizing Agents - pharmacokinetics</subject><ispartof>Nanotechnology, 2010-07, Vol.21 (29), p.295101-295101</ispartof><rights>2010 IOP Publishing Ltd 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-ba2267f77ec5689bf8e972f0d3ead578955ce3dc91463291083344bee3f91e63</citedby><cites>FETCH-LOGICAL-c489t-ba2267f77ec5689bf8e972f0d3ead578955ce3dc91463291083344bee3f91e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/0957-4484/21/29/295101/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>230,315,781,785,886,27929,27930,53835,53915</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20601762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Butterworth, K T</creatorcontrib><creatorcontrib>Coulter, J A</creatorcontrib><creatorcontrib>Jain, S</creatorcontrib><creatorcontrib>Forker, J</creatorcontrib><creatorcontrib>McMahon, S J</creatorcontrib><creatorcontrib>Schettino, G</creatorcontrib><creatorcontrib>Prise, K M</creatorcontrib><creatorcontrib>Currell, F J</creatorcontrib><creatorcontrib>Hirst, D G</creatorcontrib><title>Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy</title><title>Nanotechnology</title><addtitle>Nanotechnology</addtitle><description>High atomic number (Z) materials such as gold preferentially absorb kilovoltage x-rays compared to soft tissue and may be used to achieve local dose enhancement in tumours during treatment with ionizing radiation. Gold nanoparticles have been demonstrated as radiation dose enhancing agents in vivo and in vitro. In the present study, we used multiple endpoints to characterize the cellular cytotoxic response of a range of cell lines to 1.9 nm gold particles and measured dose modifying effects following transient exposure at low concentrations. Gold nanoparticles caused significant levels of cell type specific cytotoxicity, apoptosis and increased oxidative stress. When used as dose modifying agents, dose enhancement factors varied between the cell lines investigated with the highest enhancement being 1.9 in AGO-1522B cells at a nanoparticle concentration of 100 microg ml(-1). This study shows exposure to 1.9 nm gold particles to induce a range of cell line specific responses including decreased clonogenic survival, increased apoptosis and induction of DNA damage which may be mediated through the production of reactive oxygen species. This is the first study involving 1.9 nm nanometre sized particles to report multiple cellular responses which impact on the radiation dose modifying effect. The findings highlight the need for extensive characterization of responses to gold nanoparticles when assessing dose enhancing potential in cancer therapy.</description><subject>Apoptosis - drug effects</subject><subject>Apoptosis - radiation effects</subject><subject>Cell Growth Processes - drug effects</subject><subject>Cell Growth Processes - radiation effects</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Cell Survival - radiation effects</subject><subject>DNA Breaks, Double-Stranded</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Flow Cytometry</subject><subject>Gold - administration & dosage</subject><subject>Gold - pharmacokinetics</subject><subject>Gold - pharmacology</subject><subject>Humans</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Metal Nanoparticles - therapeutic use</subject><subject>Nonlinear Dynamics</subject><subject>Oxidation-Reduction</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - radiation effects</subject><subject>Radiation-Sensitizing Agents - administration & dosage</subject><subject>Radiation-Sensitizing Agents - chemistry</subject><subject>Radiation-Sensitizing Agents - pharmacokinetics</subject><issn>0957-4484</issn><issn>1361-6528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVFqGzEURUVpqR23WzDawMR60oxGykegmLQJGPLjfyFrJFtlPBIa2cRkM11LVpYx05iWFgKC93HPvXrch9AcyDUQIRZEVnVRlqJcUFhQObwKCHxAU2AcCl5R8RFNL9AEXfX9T0IABIXPaEIJJ1BzOkXPd0fdHnT2ocPBYXPKIYcnb3w-Yd01OOnGj6rtdrozdm-7jA-977YYruXLr26Pt6FtcNQpe9Pa_gbHkAfI6xbrGFtvRr8LCZtzQsJ5Z5OOpy_ok9Ntb7_-njO0_n63Xt4Xq8cfD8tvq8KUQuZioynltatrayou5MYJK2vqSMOsbqpayKoyljVGQskZlUM9jJXlxlrmJFjOZuh2jI2Hzd42Ztgt6VbF5Pc6nVTQXv2tdH6ntuGoGAHOqRwC-BhgUuj7ZN3FC0Sdr6HORatz0YqColKN1xiM8z9_vtje6h-AYgR8iBf1_2EqNm7g4V_-nSVeAdTKpmA</recordid><startdate>20100723</startdate><enddate>20100723</enddate><creator>Butterworth, K T</creator><creator>Coulter, J A</creator><creator>Jain, S</creator><creator>Forker, J</creator><creator>McMahon, S J</creator><creator>Schettino, G</creator><creator>Prise, K M</creator><creator>Currell, F J</creator><creator>Hirst, D G</creator><general>IOP Publishing</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20100723</creationdate><title>Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy</title><author>Butterworth, K T ; Coulter, J A ; Jain, S ; Forker, J ; McMahon, S J ; Schettino, G ; Prise, K M ; Currell, F J ; Hirst, D G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-ba2267f77ec5689bf8e972f0d3ead578955ce3dc91463291083344bee3f91e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Apoptosis - drug effects</topic><topic>Apoptosis - radiation effects</topic><topic>Cell Growth Processes - drug effects</topic><topic>Cell Growth Processes - radiation effects</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>Cell Survival - radiation effects</topic><topic>DNA Breaks, Double-Stranded</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Flow Cytometry</topic><topic>Gold - administration & dosage</topic><topic>Gold - pharmacokinetics</topic><topic>Gold - pharmacology</topic><topic>Humans</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Metal Nanoparticles - therapeutic use</topic><topic>Nonlinear Dynamics</topic><topic>Oxidation-Reduction</topic><topic>Oxidative Stress - drug effects</topic><topic>Oxidative Stress - radiation effects</topic><topic>Radiation-Sensitizing Agents - administration & dosage</topic><topic>Radiation-Sensitizing Agents - chemistry</topic><topic>Radiation-Sensitizing Agents - pharmacokinetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Butterworth, K T</creatorcontrib><creatorcontrib>Coulter, J A</creatorcontrib><creatorcontrib>Jain, S</creatorcontrib><creatorcontrib>Forker, J</creatorcontrib><creatorcontrib>McMahon, S J</creatorcontrib><creatorcontrib>Schettino, G</creatorcontrib><creatorcontrib>Prise, K M</creatorcontrib><creatorcontrib>Currell, F J</creatorcontrib><creatorcontrib>Hirst, D G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nanotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Butterworth, K T</au><au>Coulter, J A</au><au>Jain, S</au><au>Forker, J</au><au>McMahon, S J</au><au>Schettino, G</au><au>Prise, K M</au><au>Currell, F J</au><au>Hirst, D G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy</atitle><jtitle>Nanotechnology</jtitle><addtitle>Nanotechnology</addtitle><date>2010-07-23</date><risdate>2010</risdate><volume>21</volume><issue>29</issue><spage>295101</spage><epage>295101</epage><pages>295101-295101</pages><issn>0957-4484</issn><eissn>1361-6528</eissn><abstract>High atomic number (Z) materials such as gold preferentially absorb kilovoltage x-rays compared to soft tissue and may be used to achieve local dose enhancement in tumours during treatment with ionizing radiation. Gold nanoparticles have been demonstrated as radiation dose enhancing agents in vivo and in vitro. In the present study, we used multiple endpoints to characterize the cellular cytotoxic response of a range of cell lines to 1.9 nm gold particles and measured dose modifying effects following transient exposure at low concentrations. Gold nanoparticles caused significant levels of cell type specific cytotoxicity, apoptosis and increased oxidative stress. When used as dose modifying agents, dose enhancement factors varied between the cell lines investigated with the highest enhancement being 1.9 in AGO-1522B cells at a nanoparticle concentration of 100 microg ml(-1). This study shows exposure to 1.9 nm gold particles to induce a range of cell line specific responses including decreased clonogenic survival, increased apoptosis and induction of DNA damage which may be mediated through the production of reactive oxygen species. 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subjects | Apoptosis - drug effects Apoptosis - radiation effects Cell Growth Processes - drug effects Cell Growth Processes - radiation effects Cell Line, Tumor Cell Survival - drug effects Cell Survival - radiation effects DNA Breaks, Double-Stranded Dose-Response Relationship, Drug Drug Screening Assays, Antitumor Flow Cytometry Gold - administration & dosage Gold - pharmacokinetics Gold - pharmacology Humans Metal Nanoparticles - chemistry Metal Nanoparticles - therapeutic use Nonlinear Dynamics Oxidation-Reduction Oxidative Stress - drug effects Oxidative Stress - radiation effects Radiation-Sensitizing Agents - administration & dosage Radiation-Sensitizing Agents - chemistry Radiation-Sensitizing Agents - pharmacokinetics |
title | Evaluation of cytotoxicity and radiation enhancement using 1.9 nm gold particles: potential application for cancer therapy |
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