Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models
ABSTRACT Three‐dimensional (3D) cell culture models of solid tumors are currently having a tremendous impact in the in vitro screening of candidate anti‐tumoral therapies. These 3D models provide more reliable results than those provided by standard 2D in vitro cell cultures. However, 3D manufacturi...
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Veröffentlicht in: | Biotechnology and bioengineering 2014-08, Vol.111 (8), p.1672-1685 |
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description | ABSTRACT
Three‐dimensional (3D) cell culture models of solid tumors are currently having a tremendous impact in the in vitro screening of candidate anti‐tumoral therapies. These 3D models provide more reliable results than those provided by standard 2D in vitro cell cultures. However, 3D manufacturing techniques need to be further optimized in order to increase the robustness of these models and provide data that can be properly correlated with the in vivo situation. Therefore, in the present study the parameters used for producing multicellular tumor spheroids (MCTS) by liquid overlay technique (LOT) were optimized in order to produce heterogeneous cellular agglomerates comprised of cancer cells and stromal cells, during long periods. Spheroids were produced under highly controlled conditions, namely: (i) agarose coatings; (ii) horizontal stirring, and (iii) a known initial cell number. The simultaneous optimization of these parameters promoted the assembly of 3D characteristic cellular organization similar to that found in the in vivo solid tumors. Such improvements in the LOT technique promoted the assembly of highly reproducible, individual 3D spheroids, with a low cost of production and that can be used for future in vitro drug screening assays. Biotechnol. Bioeng. 2014;111: 1672–1685. © 2014 Wiley Periodicals, Inc.
Liquid Overlay Technique is one of the lowest cost and easy to handle techniques for production of tumor spheroids that mimic the solid tumors formed in vivo. In this work, the authors suggest useful guidelines to perform this in vitro cell culture technique, in order to obtain 3D cell culture models under controlled conditions. The results obtained demonstrate that the optimized parameters promote the formation of multicellular tumor spheroids with reproducible structure and uniform size and shape. |
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Three‐dimensional (3D) cell culture models of solid tumors are currently having a tremendous impact in the in vitro screening of candidate anti‐tumoral therapies. These 3D models provide more reliable results than those provided by standard 2D in vitro cell cultures. However, 3D manufacturing techniques need to be further optimized in order to increase the robustness of these models and provide data that can be properly correlated with the in vivo situation. Therefore, in the present study the parameters used for producing multicellular tumor spheroids (MCTS) by liquid overlay technique (LOT) were optimized in order to produce heterogeneous cellular agglomerates comprised of cancer cells and stromal cells, during long periods. Spheroids were produced under highly controlled conditions, namely: (i) agarose coatings; (ii) horizontal stirring, and (iii) a known initial cell number. The simultaneous optimization of these parameters promoted the assembly of 3D characteristic cellular organization similar to that found in the in vivo solid tumors. Such improvements in the LOT technique promoted the assembly of highly reproducible, individual 3D spheroids, with a low cost of production and that can be used for future in vitro drug screening assays. Biotechnol. Bioeng. 2014;111: 1672–1685. © 2014 Wiley Periodicals, Inc.
Liquid Overlay Technique is one of the lowest cost and easy to handle techniques for production of tumor spheroids that mimic the solid tumors formed in vivo. In this work, the authors suggest useful guidelines to perform this in vitro cell culture technique, in order to obtain 3D cell culture models under controlled conditions. The results obtained demonstrate that the optimized parameters promote the formation of multicellular tumor spheroids with reproducible structure and uniform size and shape.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.25210</identifier><identifier>PMID: 24615162</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>3D MCTS ; Biotechnology ; cancer ; Cell culture ; Cell Line, Tumor ; Cellular ; Coculture Techniques - instrumentation ; Coculture Techniques - methods ; Correlation analysis ; Drug Screening Assays, Antitumor - instrumentation ; Drug Screening Assays, Antitumor - methods ; Equipment Design ; Humans ; in vitro models ; In vitro testing ; LOT ; Optimization ; Spheroids ; Spheroids, Cellular - cytology ; Spheroids, Cellular - pathology ; Surgical implants ; Three dimensional ; Three dimensional models ; Tumor Cells, Cultured - cytology ; Tumor Cells, Cultured - pathology ; tumor microenvironment ; Tumors</subject><ispartof>Biotechnology and bioengineering, 2014-08, Vol.111 (8), p.1672-1685</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><rights>Copyright John Wiley and Sons, Limited Aug 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6300-5a58eda323043f6a10735af037b4a06e826d8975ced4b24944532bec4e641b9c3</citedby><cites>FETCH-LOGICAL-c6300-5a58eda323043f6a10735af037b4a06e826d8975ced4b24944532bec4e641b9c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.25210$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.25210$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24615162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Costa, Elisabete C.</creatorcontrib><creatorcontrib>Gaspar, Vítor M.</creatorcontrib><creatorcontrib>Coutinho, Paula</creatorcontrib><creatorcontrib>Correia, Ilídio J.</creatorcontrib><title>Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>ABSTRACT
Three‐dimensional (3D) cell culture models of solid tumors are currently having a tremendous impact in the in vitro screening of candidate anti‐tumoral therapies. These 3D models provide more reliable results than those provided by standard 2D in vitro cell cultures. However, 3D manufacturing techniques need to be further optimized in order to increase the robustness of these models and provide data that can be properly correlated with the in vivo situation. Therefore, in the present study the parameters used for producing multicellular tumor spheroids (MCTS) by liquid overlay technique (LOT) were optimized in order to produce heterogeneous cellular agglomerates comprised of cancer cells and stromal cells, during long periods. Spheroids were produced under highly controlled conditions, namely: (i) agarose coatings; (ii) horizontal stirring, and (iii) a known initial cell number. The simultaneous optimization of these parameters promoted the assembly of 3D characteristic cellular organization similar to that found in the in vivo solid tumors. Such improvements in the LOT technique promoted the assembly of highly reproducible, individual 3D spheroids, with a low cost of production and that can be used for future in vitro drug screening assays. Biotechnol. Bioeng. 2014;111: 1672–1685. © 2014 Wiley Periodicals, Inc.
Liquid Overlay Technique is one of the lowest cost and easy to handle techniques for production of tumor spheroids that mimic the solid tumors formed in vivo. In this work, the authors suggest useful guidelines to perform this in vitro cell culture technique, in order to obtain 3D cell culture models under controlled conditions. The results obtained demonstrate that the optimized parameters promote the formation of multicellular tumor spheroids with reproducible structure and uniform size and shape.</description><subject>3D MCTS</subject><subject>Biotechnology</subject><subject>cancer</subject><subject>Cell culture</subject><subject>Cell Line, Tumor</subject><subject>Cellular</subject><subject>Coculture Techniques - instrumentation</subject><subject>Coculture Techniques - methods</subject><subject>Correlation analysis</subject><subject>Drug Screening Assays, Antitumor - instrumentation</subject><subject>Drug Screening Assays, Antitumor - methods</subject><subject>Equipment Design</subject><subject>Humans</subject><subject>in vitro models</subject><subject>In vitro testing</subject><subject>LOT</subject><subject>Optimization</subject><subject>Spheroids</subject><subject>Spheroids, Cellular - cytology</subject><subject>Spheroids, Cellular - pathology</subject><subject>Surgical implants</subject><subject>Three dimensional</subject><subject>Three dimensional models</subject><subject>Tumor Cells, Cultured - cytology</subject><subject>Tumor Cells, Cultured - pathology</subject><subject>tumor microenvironment</subject><subject>Tumors</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhiMEokvhwB9AlrjQQ9rxZ-IjLaVUqihCRe3NcpwJdUnWi-0Ay6_Hy7Y9ICE4jWb0zKMZvVX1nMI-BWAHnc_7TDIKD6oFBd3UwDQ8rBYAoGouNdupnqR0U9qmVepxtcOEopIqtqguz1fZT_6nzT4sSRjI6L_OvifhG8bRrklGd70sIyQ5kCHEaR5tRnKNGWP4jEvvCH9DXKjdPOY5YiJT6HFMT6tHgx0TPrutu9Wnt8cXR-_qs_OT06PXZ7VTHKCWVrbYW844CD4oS6Hh0g7Am05YUNgy1be6kQ570TGhhZCcdegEKkE77fhu9WrrXcVQrkzZTD45HEe7xDAnQxsORdqK9t-olEJLxin9D1RQ3kgOG-vLP9CbMMdl-XlD8abVvFWF2ttSLoaUIg5mFf1k49pQMJsMTcnQ_M6wsC9ujXM3YX9P3oVWgIMt8N2PuP67yRyeXtwp6-2GTxl_3G_Y-MWopjxiLt-fmCv9gX_kV9oA_wWcarKE</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Costa, Elisabete C.</creator><creator>Gaspar, Vítor M.</creator><creator>Coutinho, Paula</creator><creator>Correia, Ilídio J.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201408</creationdate><title>Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models</title><author>Costa, Elisabete C. ; Gaspar, Vítor M. ; Coutinho, Paula ; Correia, Ilídio J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6300-5a58eda323043f6a10735af037b4a06e826d8975ced4b24944532bec4e641b9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>3D MCTS</topic><topic>Biotechnology</topic><topic>cancer</topic><topic>Cell culture</topic><topic>Cell Line, Tumor</topic><topic>Cellular</topic><topic>Coculture Techniques - instrumentation</topic><topic>Coculture Techniques - methods</topic><topic>Correlation analysis</topic><topic>Drug Screening Assays, Antitumor - instrumentation</topic><topic>Drug Screening Assays, Antitumor - methods</topic><topic>Equipment Design</topic><topic>Humans</topic><topic>in vitro models</topic><topic>In vitro testing</topic><topic>LOT</topic><topic>Optimization</topic><topic>Spheroids</topic><topic>Spheroids, Cellular - cytology</topic><topic>Spheroids, Cellular - pathology</topic><topic>Surgical implants</topic><topic>Three dimensional</topic><topic>Three dimensional models</topic><topic>Tumor Cells, Cultured - cytology</topic><topic>Tumor Cells, Cultured - pathology</topic><topic>tumor microenvironment</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Costa, Elisabete C.</creatorcontrib><creatorcontrib>Gaspar, Vítor M.</creatorcontrib><creatorcontrib>Coutinho, Paula</creatorcontrib><creatorcontrib>Correia, Ilídio J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Costa, Elisabete C.</au><au>Gaspar, Vítor M.</au><au>Coutinho, Paula</au><au>Correia, Ilídio J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>2014-08</date><risdate>2014</risdate><volume>111</volume><issue>8</issue><spage>1672</spage><epage>1685</epage><pages>1672-1685</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>ABSTRACT
Three‐dimensional (3D) cell culture models of solid tumors are currently having a tremendous impact in the in vitro screening of candidate anti‐tumoral therapies. These 3D models provide more reliable results than those provided by standard 2D in vitro cell cultures. However, 3D manufacturing techniques need to be further optimized in order to increase the robustness of these models and provide data that can be properly correlated with the in vivo situation. Therefore, in the present study the parameters used for producing multicellular tumor spheroids (MCTS) by liquid overlay technique (LOT) were optimized in order to produce heterogeneous cellular agglomerates comprised of cancer cells and stromal cells, during long periods. Spheroids were produced under highly controlled conditions, namely: (i) agarose coatings; (ii) horizontal stirring, and (iii) a known initial cell number. The simultaneous optimization of these parameters promoted the assembly of 3D characteristic cellular organization similar to that found in the in vivo solid tumors. Such improvements in the LOT technique promoted the assembly of highly reproducible, individual 3D spheroids, with a low cost of production and that can be used for future in vitro drug screening assays. Biotechnol. Bioeng. 2014;111: 1672–1685. © 2014 Wiley Periodicals, Inc.
Liquid Overlay Technique is one of the lowest cost and easy to handle techniques for production of tumor spheroids that mimic the solid tumors formed in vivo. In this work, the authors suggest useful guidelines to perform this in vitro cell culture technique, in order to obtain 3D cell culture models under controlled conditions. The results obtained demonstrate that the optimized parameters promote the formation of multicellular tumor spheroids with reproducible structure and uniform size and shape.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24615162</pmid><doi>10.1002/bit.25210</doi><tpages>14</tpages></addata></record> |
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subjects | 3D MCTS Biotechnology cancer Cell culture Cell Line, Tumor Cellular Coculture Techniques - instrumentation Coculture Techniques - methods Correlation analysis Drug Screening Assays, Antitumor - instrumentation Drug Screening Assays, Antitumor - methods Equipment Design Humans in vitro models In vitro testing LOT Optimization Spheroids Spheroids, Cellular - cytology Spheroids, Cellular - pathology Surgical implants Three dimensional Three dimensional models Tumor Cells, Cultured - cytology Tumor Cells, Cultured - pathology tumor microenvironment Tumors |
title | Optimization of liquid overlay technique to formulate heterogenic 3D co-cultures models |
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