The use of nanoimprinted scaffolds as 3D culture models to facilitate spontaneous tumor cell migration and well-regulated spheroid formation

Abstract Two-dimensional (2D) cell cultures are essential for drug development and tumor research. However, the limitations of 2D cultures are widely recognized, and a better technique is needed. Recent studies have indicated that a strong physical contact between cells and 2D substrates induces cel...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biomaterials 2011-09, Vol.32 (26), p.6052-6058
Hauptverfasser: Yoshii, Yukie, Waki, Atsuo, Yoshida, Kaori, Kakezuka, Anna, Kobayashi, Maki, Namiki, Hideo, Kuroda, Yusei, Kiyono, Yasushi, Yoshii, Hiroshi, Furukawa, Takako, Asai, Tatsuya, Okazawa, Hidehiko, Gelovani, Juri G, Fujibayashi, Yasuhisa
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6058
container_issue 26
container_start_page 6052
container_title Biomaterials
container_volume 32
creator Yoshii, Yukie
Waki, Atsuo
Yoshida, Kaori
Kakezuka, Anna
Kobayashi, Maki
Namiki, Hideo
Kuroda, Yusei
Kiyono, Yasushi
Yoshii, Hiroshi
Furukawa, Takako
Asai, Tatsuya
Okazawa, Hidehiko
Gelovani, Juri G
Fujibayashi, Yasuhisa
description Abstract Two-dimensional (2D) cell cultures are essential for drug development and tumor research. However, the limitations of 2D cultures are widely recognized, and a better technique is needed. Recent studies have indicated that a strong physical contact between cells and 2D substrates induces cellular characteristics that differ from those of tumors growing in vivo . 3D cell cultures using various substrates are then developing; nevertheless, conventional approaches have failed in maintenance of cellular proliferation and viability, uniformity, reproducibility, and/or simplicity of these assays. Here, we developed a 3D culture system with inorganic nanoscale scaffolding using nanoimprinting technology (nano-culture plates), which reproduced the characteristics of tumor cells growing in vivo . Diminished cell-to-substrate physical contact facilitated spontaneous tumor cell migration, intercellular adhesion, and multi-cellular 3D-spheroid formation while maintaining cellular proliferation and viability. The resulting multi-cellular spheroids formed hypoxic core regions similar to tumors growing in vivo . This technology allows creating uniform and highly-reproducible 3D cultures, which is easily applicable for microscopic and spectrophotometric assays, which can be used for high-throughput/high-content screening of anticancer drugs and should accelerate discovery of more effective anticancer therapies.
doi_str_mv 10.1016/j.biomaterials.2011.04.076
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_883016254</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0142961211004984</els_id><sourcerecordid>883016254</sourcerecordid><originalsourceid>FETCH-LOGICAL-c576t-7af8733f674d6f9ff6afa13260c5f2a799b13ee113078b83ff9ddce772a7329a3</originalsourceid><addsrcrecordid>eNqNUstuFDEQtBCILIFfQBYXTrP4NWMPBySU8JIicSCcLa_dTrzM2IvtAeUf-Gg82YAQFzhZ7a7u6q5qhJ5RsqWEDi_2211Is6mQg5nKlhFKt0RsiRzuoQ1VUnX9SPr7aEOoYN04UHaCHpWyJy0mgj1EJ4wOgnCpNujH5TXgpQBOHkcTU5gPOcQKDhdrvE-TK9gUzM-xXaa6ZMBzcjAVXBP2xoYp1DYILocUq4mQlpZZ5pSxhWnCc7jKpoYUsYkOf29fXYarZTK3BIdryCk47FOeb1GP0QPfNoInd-8p-vz2zeXZ--7i47sPZ68vOtvLoXbSeCU594MUbvCj94PxhnI2ENt7ZuQ47igHoJQTqXaKez86Z0HKluNsNPwUPT_2PeT0dYFS9RzKOvBxA60UbzqzXvwbKXuieiFJQ748Im1OpWTwugk5m3yjKdGrbXqv_7RNr7ZpInSzrRU_vaNZdjO436W_fGqA8yOgSQ_fAmRdbIBowYUMtmqXwv_xvPqrjZ1CDNZMX-AGyj4tOa41VBemif60HtB6P5QSIkYl-E9E4sgj</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>875085470</pqid></control><display><type>article</type><title>The use of nanoimprinted scaffolds as 3D culture models to facilitate spontaneous tumor cell migration and well-regulated spheroid formation</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Yoshii, Yukie ; Waki, Atsuo ; Yoshida, Kaori ; Kakezuka, Anna ; Kobayashi, Maki ; Namiki, Hideo ; Kuroda, Yusei ; Kiyono, Yasushi ; Yoshii, Hiroshi ; Furukawa, Takako ; Asai, Tatsuya ; Okazawa, Hidehiko ; Gelovani, Juri G ; Fujibayashi, Yasuhisa</creator><creatorcontrib>Yoshii, Yukie ; Waki, Atsuo ; Yoshida, Kaori ; Kakezuka, Anna ; Kobayashi, Maki ; Namiki, Hideo ; Kuroda, Yusei ; Kiyono, Yasushi ; Yoshii, Hiroshi ; Furukawa, Takako ; Asai, Tatsuya ; Okazawa, Hidehiko ; Gelovani, Juri G ; Fujibayashi, Yasuhisa</creatorcontrib><description>Abstract Two-dimensional (2D) cell cultures are essential for drug development and tumor research. However, the limitations of 2D cultures are widely recognized, and a better technique is needed. Recent studies have indicated that a strong physical contact between cells and 2D substrates induces cellular characteristics that differ from those of tumors growing in vivo . 3D cell cultures using various substrates are then developing; nevertheless, conventional approaches have failed in maintenance of cellular proliferation and viability, uniformity, reproducibility, and/or simplicity of these assays. Here, we developed a 3D culture system with inorganic nanoscale scaffolding using nanoimprinting technology (nano-culture plates), which reproduced the characteristics of tumor cells growing in vivo . Diminished cell-to-substrate physical contact facilitated spontaneous tumor cell migration, intercellular adhesion, and multi-cellular 3D-spheroid formation while maintaining cellular proliferation and viability. The resulting multi-cellular spheroids formed hypoxic core regions similar to tumors growing in vivo . This technology allows creating uniform and highly-reproducible 3D cultures, which is easily applicable for microscopic and spectrophotometric assays, which can be used for high-throughput/high-content screening of anticancer drugs and should accelerate discovery of more effective anticancer therapies.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2011.04.076</identifier><identifier>PMID: 21640378</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>3D cell culture ; Advanced Basic Science ; Animals ; Cell Culture Techniques - methods ; Cell Line, Tumor ; Cell Movement - physiology ; Cell Proliferation ; Cell Survival - physiology ; Dentistry ; Humans ; Hypoxia ; Mice ; Multi-cellular spheroid ; Nanoimprinting technology ; Spheroids, Cellular - cytology ; Tissue Scaffolds ; Tumor cell migration</subject><ispartof>Biomaterials, 2011-09, Vol.32 (26), p.6052-6058</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c576t-7af8733f674d6f9ff6afa13260c5f2a799b13ee113078b83ff9ddce772a7329a3</citedby><cites>FETCH-LOGICAL-c576t-7af8733f674d6f9ff6afa13260c5f2a799b13ee113078b83ff9ddce772a7329a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0142961211004984$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21640378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoshii, Yukie</creatorcontrib><creatorcontrib>Waki, Atsuo</creatorcontrib><creatorcontrib>Yoshida, Kaori</creatorcontrib><creatorcontrib>Kakezuka, Anna</creatorcontrib><creatorcontrib>Kobayashi, Maki</creatorcontrib><creatorcontrib>Namiki, Hideo</creatorcontrib><creatorcontrib>Kuroda, Yusei</creatorcontrib><creatorcontrib>Kiyono, Yasushi</creatorcontrib><creatorcontrib>Yoshii, Hiroshi</creatorcontrib><creatorcontrib>Furukawa, Takako</creatorcontrib><creatorcontrib>Asai, Tatsuya</creatorcontrib><creatorcontrib>Okazawa, Hidehiko</creatorcontrib><creatorcontrib>Gelovani, Juri G</creatorcontrib><creatorcontrib>Fujibayashi, Yasuhisa</creatorcontrib><title>The use of nanoimprinted scaffolds as 3D culture models to facilitate spontaneous tumor cell migration and well-regulated spheroid formation</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Abstract Two-dimensional (2D) cell cultures are essential for drug development and tumor research. However, the limitations of 2D cultures are widely recognized, and a better technique is needed. Recent studies have indicated that a strong physical contact between cells and 2D substrates induces cellular characteristics that differ from those of tumors growing in vivo . 3D cell cultures using various substrates are then developing; nevertheless, conventional approaches have failed in maintenance of cellular proliferation and viability, uniformity, reproducibility, and/or simplicity of these assays. Here, we developed a 3D culture system with inorganic nanoscale scaffolding using nanoimprinting technology (nano-culture plates), which reproduced the characteristics of tumor cells growing in vivo . Diminished cell-to-substrate physical contact facilitated spontaneous tumor cell migration, intercellular adhesion, and multi-cellular 3D-spheroid formation while maintaining cellular proliferation and viability. The resulting multi-cellular spheroids formed hypoxic core regions similar to tumors growing in vivo . This technology allows creating uniform and highly-reproducible 3D cultures, which is easily applicable for microscopic and spectrophotometric assays, which can be used for high-throughput/high-content screening of anticancer drugs and should accelerate discovery of more effective anticancer therapies.</description><subject>3D cell culture</subject><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement - physiology</subject><subject>Cell Proliferation</subject><subject>Cell Survival - physiology</subject><subject>Dentistry</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Mice</subject><subject>Multi-cellular spheroid</subject><subject>Nanoimprinting technology</subject><subject>Spheroids, Cellular - cytology</subject><subject>Tissue Scaffolds</subject><subject>Tumor cell migration</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUstuFDEQtBCILIFfQBYXTrP4NWMPBySU8JIicSCcLa_dTrzM2IvtAeUf-Gg82YAQFzhZ7a7u6q5qhJ5RsqWEDi_2211Is6mQg5nKlhFKt0RsiRzuoQ1VUnX9SPr7aEOoYN04UHaCHpWyJy0mgj1EJ4wOgnCpNujH5TXgpQBOHkcTU5gPOcQKDhdrvE-TK9gUzM-xXaa6ZMBzcjAVXBP2xoYp1DYILocUq4mQlpZZ5pSxhWnCc7jKpoYUsYkOf29fXYarZTK3BIdryCk47FOeb1GP0QPfNoInd-8p-vz2zeXZ--7i47sPZ68vOtvLoXbSeCU594MUbvCj94PxhnI2ENt7ZuQ47igHoJQTqXaKez86Z0HKluNsNPwUPT_2PeT0dYFS9RzKOvBxA60UbzqzXvwbKXuieiFJQ748Im1OpWTwugk5m3yjKdGrbXqv_7RNr7ZpInSzrRU_vaNZdjO436W_fGqA8yOgSQ_fAmRdbIBowYUMtmqXwv_xvPqrjZ1CDNZMX-AGyj4tOa41VBemif60HtB6P5QSIkYl-E9E4sgj</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Yoshii, Yukie</creator><creator>Waki, Atsuo</creator><creator>Yoshida, Kaori</creator><creator>Kakezuka, Anna</creator><creator>Kobayashi, Maki</creator><creator>Namiki, Hideo</creator><creator>Kuroda, Yusei</creator><creator>Kiyono, Yasushi</creator><creator>Yoshii, Hiroshi</creator><creator>Furukawa, Takako</creator><creator>Asai, Tatsuya</creator><creator>Okazawa, Hidehiko</creator><creator>Gelovani, Juri G</creator><creator>Fujibayashi, Yasuhisa</creator><general>Elsevier Ltd</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>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20110901</creationdate><title>The use of nanoimprinted scaffolds as 3D culture models to facilitate spontaneous tumor cell migration and well-regulated spheroid formation</title><author>Yoshii, Yukie ; Waki, Atsuo ; Yoshida, Kaori ; Kakezuka, Anna ; Kobayashi, Maki ; Namiki, Hideo ; Kuroda, Yusei ; Kiyono, Yasushi ; Yoshii, Hiroshi ; Furukawa, Takako ; Asai, Tatsuya ; Okazawa, Hidehiko ; Gelovani, Juri G ; Fujibayashi, Yasuhisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c576t-7af8733f674d6f9ff6afa13260c5f2a799b13ee113078b83ff9ddce772a7329a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>3D cell culture</topic><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement - physiology</topic><topic>Cell Proliferation</topic><topic>Cell Survival - physiology</topic><topic>Dentistry</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>Mice</topic><topic>Multi-cellular spheroid</topic><topic>Nanoimprinting technology</topic><topic>Spheroids, Cellular - cytology</topic><topic>Tissue Scaffolds</topic><topic>Tumor cell migration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshii, Yukie</creatorcontrib><creatorcontrib>Waki, Atsuo</creatorcontrib><creatorcontrib>Yoshida, Kaori</creatorcontrib><creatorcontrib>Kakezuka, Anna</creatorcontrib><creatorcontrib>Kobayashi, Maki</creatorcontrib><creatorcontrib>Namiki, Hideo</creatorcontrib><creatorcontrib>Kuroda, Yusei</creatorcontrib><creatorcontrib>Kiyono, Yasushi</creatorcontrib><creatorcontrib>Yoshii, Hiroshi</creatorcontrib><creatorcontrib>Furukawa, Takako</creatorcontrib><creatorcontrib>Asai, Tatsuya</creatorcontrib><creatorcontrib>Okazawa, Hidehiko</creatorcontrib><creatorcontrib>Gelovani, Juri G</creatorcontrib><creatorcontrib>Fujibayashi, Yasuhisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshii, Yukie</au><au>Waki, Atsuo</au><au>Yoshida, Kaori</au><au>Kakezuka, Anna</au><au>Kobayashi, Maki</au><au>Namiki, Hideo</au><au>Kuroda, Yusei</au><au>Kiyono, Yasushi</au><au>Yoshii, Hiroshi</au><au>Furukawa, Takako</au><au>Asai, Tatsuya</au><au>Okazawa, Hidehiko</au><au>Gelovani, Juri G</au><au>Fujibayashi, Yasuhisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The use of nanoimprinted scaffolds as 3D culture models to facilitate spontaneous tumor cell migration and well-regulated spheroid formation</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>32</volume><issue>26</issue><spage>6052</spage><epage>6058</epage><pages>6052-6058</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract Two-dimensional (2D) cell cultures are essential for drug development and tumor research. However, the limitations of 2D cultures are widely recognized, and a better technique is needed. Recent studies have indicated that a strong physical contact between cells and 2D substrates induces cellular characteristics that differ from those of tumors growing in vivo . 3D cell cultures using various substrates are then developing; nevertheless, conventional approaches have failed in maintenance of cellular proliferation and viability, uniformity, reproducibility, and/or simplicity of these assays. Here, we developed a 3D culture system with inorganic nanoscale scaffolding using nanoimprinting technology (nano-culture plates), which reproduced the characteristics of tumor cells growing in vivo . Diminished cell-to-substrate physical contact facilitated spontaneous tumor cell migration, intercellular adhesion, and multi-cellular 3D-spheroid formation while maintaining cellular proliferation and viability. The resulting multi-cellular spheroids formed hypoxic core regions similar to tumors growing in vivo . This technology allows creating uniform and highly-reproducible 3D cultures, which is easily applicable for microscopic and spectrophotometric assays, which can be used for high-throughput/high-content screening of anticancer drugs and should accelerate discovery of more effective anticancer therapies.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>21640378</pmid><doi>10.1016/j.biomaterials.2011.04.076</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0142-9612
ispartof Biomaterials, 2011-09, Vol.32 (26), p.6052-6058
issn 0142-9612
1878-5905
language eng
recordid cdi_proquest_miscellaneous_883016254
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects 3D cell culture
Advanced Basic Science
Animals
Cell Culture Techniques - methods
Cell Line, Tumor
Cell Movement - physiology
Cell Proliferation
Cell Survival - physiology
Dentistry
Humans
Hypoxia
Mice
Multi-cellular spheroid
Nanoimprinting technology
Spheroids, Cellular - cytology
Tissue Scaffolds
Tumor cell migration
title The use of nanoimprinted scaffolds as 3D culture models to facilitate spontaneous tumor cell migration and well-regulated spheroid formation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T20%3A27%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20use%20of%20nanoimprinted%20scaffolds%20as%203D%20culture%20models%20to%20facilitate%20spontaneous%20tumor%20cell%20migration%20and%20well-regulated%20spheroid%20formation&rft.jtitle=Biomaterials&rft.au=Yoshii,%20Yukie&rft.date=2011-09-01&rft.volume=32&rft.issue=26&rft.spage=6052&rft.epage=6058&rft.pages=6052-6058&rft.issn=0142-9612&rft.eissn=1878-5905&rft_id=info:doi/10.1016/j.biomaterials.2011.04.076&rft_dat=%3Cproquest_cross%3E883016254%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=875085470&rft_id=info:pmid/21640378&rft_els_id=1_s2_0_S0142961211004984&rfr_iscdi=true