In vitro cell transformation induced by synthetic amorphous silica nanoparticles
•The Bhas 42 cell transformation assay is suitable for particle-type substances.•Four different silica nanoparticles induced cell transformation in Bhas 42 cells.•The four silica nanoparticles act as tumor-promoter substances in the Bhas 42 model. Synthetic amorphous silica nanoparticles (SAS) are a...
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Veröffentlicht in: | Mutation research 2017-11, Vol.823, p.22-27 |
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creator | Fontana, Caroline Kirsch, Anaïs Seidel, Carole Marpeaux, Léa Darne, Christian Gaté, Laurent Remy, Aurélie Guichard, Yves |
description | •The Bhas 42 cell transformation assay is suitable for particle-type substances.•Four different silica nanoparticles induced cell transformation in Bhas 42 cells.•The four silica nanoparticles act as tumor-promoter substances in the Bhas 42 model.
Synthetic amorphous silica nanoparticles (SAS) are among the most widely produced and used nanomaterials, but little is known about their carcinogenic potential. This study aims to evaluate the ability of four different SAS, two precipitated, NM-200 and NM-201, and two pyrogenic, NM-202 and NM-203, to induce the transformation process. For this, we used the recently developed in vitro Bhas 42 cell transformation assay (CTA). The genome of the transgenic Bhas 42 cells contains several copies of the v-Ha-ras gene, making them particularly sensitive to tumor-promoter agents. The Bhas 42 CTA, which includes an initiation assay and a promotion assay, was validated in our laboratory using known soluble carcinogenic substances. Its suitability for particle-type substances was verified by using quartz Min-U-Sil 5 (Min-U-Sil) and diatomaceous earth (DE) microparticles. As expected given their known transforming properties, Min-U-Sil responded positively in the Bhas 42 CTA and DE responded negatively. Transformation assays were performed with SAS at concentrations ranging from 2μg/cm2 to 80μg/cm2. Results showed that all SAS have the capacity to induce transformed foci, interestingly only in the promotion assay, suggesting a mode of action similar to tumor-promoter substances. NM-203 exhibited transforming activity at a lower concentration than the other SAS. In conclusion, this study showed for the first time the transforming potential of different SAS, which act as tumor-promoter substances in the Bhas 42 model of cell transformation. |
doi_str_mv | 10.1016/j.mrgentox.2017.08.002 |
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Synthetic amorphous silica nanoparticles (SAS) are among the most widely produced and used nanomaterials, but little is known about their carcinogenic potential. This study aims to evaluate the ability of four different SAS, two precipitated, NM-200 and NM-201, and two pyrogenic, NM-202 and NM-203, to induce the transformation process. For this, we used the recently developed in vitro Bhas 42 cell transformation assay (CTA). The genome of the transgenic Bhas 42 cells contains several copies of the v-Ha-ras gene, making them particularly sensitive to tumor-promoter agents. The Bhas 42 CTA, which includes an initiation assay and a promotion assay, was validated in our laboratory using known soluble carcinogenic substances. Its suitability for particle-type substances was verified by using quartz Min-U-Sil 5 (Min-U-Sil) and diatomaceous earth (DE) microparticles. As expected given their known transforming properties, Min-U-Sil responded positively in the Bhas 42 CTA and DE responded negatively. Transformation assays were performed with SAS at concentrations ranging from 2μg/cm2 to 80μg/cm2. Results showed that all SAS have the capacity to induce transformed foci, interestingly only in the promotion assay, suggesting a mode of action similar to tumor-promoter substances. NM-203 exhibited transforming activity at a lower concentration than the other SAS. In conclusion, this study showed for the first time the transforming potential of different SAS, which act as tumor-promoter substances in the Bhas 42 model of cell transformation.</description><identifier>ISSN: 1383-5718</identifier><identifier>EISSN: 1879-3592</identifier><identifier>EISSN: 1873-135X</identifier><identifier>DOI: 10.1016/j.mrgentox.2017.08.002</identifier><identifier>PMID: 28985944</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; BALB 3T3 Cells ; Bhas 42 ; Carcinogenesis - drug effects ; Carcinogenesis - metabolism ; Carcinogenicity Tests ; Carcinogens - toxicity ; Cell transformation assay ; Cell Transformation, Neoplastic - chemically induced ; Cell Transformation, Neoplastic - metabolism ; Chemical engineering ; Chemical Sciences ; Engineering Sciences ; Genes, ras ; Life Sciences ; Mice ; Micro and nanotechnologies ; Microelectronics ; Nanomaterial ; Nanoparticles - toxicity ; Particle Size ; Silicon Dioxide - toxicity ; Synthetic amorphous silica ; Toxicology</subject><ispartof>Mutation research, 2017-11, Vol.823, p.22-27</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>Attribution - NonCommercial - NoDerivatives</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-2079641361f145e44a16a1cdf1e2ea18c00b17f96226aca58f47f705076b7c7f3</citedby><cites>FETCH-LOGICAL-c516t-2079641361f145e44a16a1cdf1e2ea18c00b17f96226aca58f47f705076b7c7f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mrgentox.2017.08.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28985944$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01667424$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Fontana, Caroline</creatorcontrib><creatorcontrib>Kirsch, Anaïs</creatorcontrib><creatorcontrib>Seidel, Carole</creatorcontrib><creatorcontrib>Marpeaux, Léa</creatorcontrib><creatorcontrib>Darne, Christian</creatorcontrib><creatorcontrib>Gaté, Laurent</creatorcontrib><creatorcontrib>Remy, Aurélie</creatorcontrib><creatorcontrib>Guichard, Yves</creatorcontrib><title>In vitro cell transformation induced by synthetic amorphous silica nanoparticles</title><title>Mutation research</title><addtitle>Mutat Res</addtitle><description>•The Bhas 42 cell transformation assay is suitable for particle-type substances.•Four different silica nanoparticles induced cell transformation in Bhas 42 cells.•The four silica nanoparticles act as tumor-promoter substances in the Bhas 42 model.
Synthetic amorphous silica nanoparticles (SAS) are among the most widely produced and used nanomaterials, but little is known about their carcinogenic potential. This study aims to evaluate the ability of four different SAS, two precipitated, NM-200 and NM-201, and two pyrogenic, NM-202 and NM-203, to induce the transformation process. For this, we used the recently developed in vitro Bhas 42 cell transformation assay (CTA). The genome of the transgenic Bhas 42 cells contains several copies of the v-Ha-ras gene, making them particularly sensitive to tumor-promoter agents. The Bhas 42 CTA, which includes an initiation assay and a promotion assay, was validated in our laboratory using known soluble carcinogenic substances. Its suitability for particle-type substances was verified by using quartz Min-U-Sil 5 (Min-U-Sil) and diatomaceous earth (DE) microparticles. As expected given their known transforming properties, Min-U-Sil responded positively in the Bhas 42 CTA and DE responded negatively. Transformation assays were performed with SAS at concentrations ranging from 2μg/cm2 to 80μg/cm2. Results showed that all SAS have the capacity to induce transformed foci, interestingly only in the promotion assay, suggesting a mode of action similar to tumor-promoter substances. NM-203 exhibited transforming activity at a lower concentration than the other SAS. In conclusion, this study showed for the first time the transforming potential of different SAS, which act as tumor-promoter substances in the Bhas 42 model of cell transformation.</description><subject>Animals</subject><subject>BALB 3T3 Cells</subject><subject>Bhas 42</subject><subject>Carcinogenesis - drug effects</subject><subject>Carcinogenesis - metabolism</subject><subject>Carcinogenicity Tests</subject><subject>Carcinogens - toxicity</subject><subject>Cell transformation assay</subject><subject>Cell Transformation, Neoplastic - chemically induced</subject><subject>Cell Transformation, Neoplastic - metabolism</subject><subject>Chemical engineering</subject><subject>Chemical Sciences</subject><subject>Engineering Sciences</subject><subject>Genes, ras</subject><subject>Life Sciences</subject><subject>Mice</subject><subject>Micro and nanotechnologies</subject><subject>Microelectronics</subject><subject>Nanomaterial</subject><subject>Nanoparticles - toxicity</subject><subject>Particle Size</subject><subject>Silicon Dioxide - toxicity</subject><subject>Synthetic amorphous silica</subject><subject>Toxicology</subject><issn>1383-5718</issn><issn>1879-3592</issn><issn>1873-135X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PAyEQhonR-P0XDFcPuzIsC-xNY_xKmuhBz4SyYGl2oYFtY_-9NFWvnpgwzzuTeRC6AlIDAX6zrMf0acMUv2pKQNRE1oTQA3QKUnRV03b0sNSNbKpWgDxBZzkvC0AaIo_RCZWdbDvGTtHbS8AbP6WIjR0GPCUdsotp1JOPAfvQr43t8XyL8zZMCzt5g_UY02oR1xlnP3ijcdAhrnQqvcHmC3Tk9JDt5c97jj4eH97vn6vZ69PL_d2sMi3wqaJEdJxBw8EBay1jGrgG0zuw1GqQhpA5CNdxSrk2upWOCSdISwSfCyNcc46u93MXelCr5Eedtipqr57vZmr3VyxxwSjbQGH5njUp5pys-wsAUTudaql-daqdTkWkKrZK8GofXK3no-3_Yr_-CnC7B2w5deNtUtl4G4ozn6yZVB_9fzu-AVRxioQ</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Fontana, Caroline</creator><creator>Kirsch, Anaïs</creator><creator>Seidel, Carole</creator><creator>Marpeaux, Léa</creator><creator>Darne, Christian</creator><creator>Gaté, Laurent</creator><creator>Remy, Aurélie</creator><creator>Guichard, Yves</creator><general>Elsevier B.V</general><general>Elsevier</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>1XC</scope><scope>VOOES</scope></search><sort><creationdate>201711</creationdate><title>In vitro cell transformation induced by synthetic amorphous silica nanoparticles</title><author>Fontana, Caroline ; Kirsch, Anaïs ; Seidel, Carole ; Marpeaux, Léa ; Darne, Christian ; Gaté, Laurent ; Remy, Aurélie ; Guichard, Yves</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-2079641361f145e44a16a1cdf1e2ea18c00b17f96226aca58f47f705076b7c7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>BALB 3T3 Cells</topic><topic>Bhas 42</topic><topic>Carcinogenesis - drug effects</topic><topic>Carcinogenesis - metabolism</topic><topic>Carcinogenicity Tests</topic><topic>Carcinogens - toxicity</topic><topic>Cell transformation assay</topic><topic>Cell Transformation, Neoplastic - chemically induced</topic><topic>Cell Transformation, Neoplastic - metabolism</topic><topic>Chemical engineering</topic><topic>Chemical Sciences</topic><topic>Engineering Sciences</topic><topic>Genes, ras</topic><topic>Life Sciences</topic><topic>Mice</topic><topic>Micro and nanotechnologies</topic><topic>Microelectronics</topic><topic>Nanomaterial</topic><topic>Nanoparticles - toxicity</topic><topic>Particle Size</topic><topic>Silicon Dioxide - toxicity</topic><topic>Synthetic amorphous silica</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fontana, Caroline</creatorcontrib><creatorcontrib>Kirsch, Anaïs</creatorcontrib><creatorcontrib>Seidel, Carole</creatorcontrib><creatorcontrib>Marpeaux, Léa</creatorcontrib><creatorcontrib>Darne, Christian</creatorcontrib><creatorcontrib>Gaté, Laurent</creatorcontrib><creatorcontrib>Remy, Aurélie</creatorcontrib><creatorcontrib>Guichard, Yves</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Mutation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fontana, Caroline</au><au>Kirsch, Anaïs</au><au>Seidel, Carole</au><au>Marpeaux, Léa</au><au>Darne, Christian</au><au>Gaté, Laurent</au><au>Remy, Aurélie</au><au>Guichard, Yves</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro cell transformation induced by synthetic amorphous silica nanoparticles</atitle><jtitle>Mutation research</jtitle><addtitle>Mutat Res</addtitle><date>2017-11</date><risdate>2017</risdate><volume>823</volume><spage>22</spage><epage>27</epage><pages>22-27</pages><issn>1383-5718</issn><eissn>1879-3592</eissn><eissn>1873-135X</eissn><abstract>•The Bhas 42 cell transformation assay is suitable for particle-type substances.•Four different silica nanoparticles induced cell transformation in Bhas 42 cells.•The four silica nanoparticles act as tumor-promoter substances in the Bhas 42 model.
Synthetic amorphous silica nanoparticles (SAS) are among the most widely produced and used nanomaterials, but little is known about their carcinogenic potential. This study aims to evaluate the ability of four different SAS, two precipitated, NM-200 and NM-201, and two pyrogenic, NM-202 and NM-203, to induce the transformation process. For this, we used the recently developed in vitro Bhas 42 cell transformation assay (CTA). The genome of the transgenic Bhas 42 cells contains several copies of the v-Ha-ras gene, making them particularly sensitive to tumor-promoter agents. The Bhas 42 CTA, which includes an initiation assay and a promotion assay, was validated in our laboratory using known soluble carcinogenic substances. Its suitability for particle-type substances was verified by using quartz Min-U-Sil 5 (Min-U-Sil) and diatomaceous earth (DE) microparticles. As expected given their known transforming properties, Min-U-Sil responded positively in the Bhas 42 CTA and DE responded negatively. Transformation assays were performed with SAS at concentrations ranging from 2μg/cm2 to 80μg/cm2. Results showed that all SAS have the capacity to induce transformed foci, interestingly only in the promotion assay, suggesting a mode of action similar to tumor-promoter substances. NM-203 exhibited transforming activity at a lower concentration than the other SAS. In conclusion, this study showed for the first time the transforming potential of different SAS, which act as tumor-promoter substances in the Bhas 42 model of cell transformation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28985944</pmid><doi>10.1016/j.mrgentox.2017.08.002</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals BALB 3T3 Cells Bhas 42 Carcinogenesis - drug effects Carcinogenesis - metabolism Carcinogenicity Tests Carcinogens - toxicity Cell transformation assay Cell Transformation, Neoplastic - chemically induced Cell Transformation, Neoplastic - metabolism Chemical engineering Chemical Sciences Engineering Sciences Genes, ras Life Sciences Mice Micro and nanotechnologies Microelectronics Nanomaterial Nanoparticles - toxicity Particle Size Silicon Dioxide - toxicity Synthetic amorphous silica Toxicology |
title | In vitro cell transformation induced by synthetic amorphous silica nanoparticles |
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