Establishment of Pancreatic Cancer-Derived Tumor Organoids and Fibroblasts From Fresh Tissue
Tumor organoids are three-dimensional (3D) ex vivo tumor models that recapitulate the biological key features of the original primary tumor tissues. Patient-derived tumor organoids have been used in translational cancer research and can be applied to assess treatment sensitivity and resistance, cell...
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Veröffentlicht in: | Journal of visualized experiments 2023-05 (195) |
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creator | Díaz-Alejo, Jesús Frutos April-Monn, Simon Cihova, Marina Buocikova, Verona Villalón López, Jorge Urbanova, Maria Lechuga, Carmen G Tomas, Miroslav Dubovan, Peter Sánchez, Bárbara Luna Páez, Sonia Camaño Sanjuanbenito, Alfonso Lobo, Eduardo Romio de la Heras, Estefanía Guerra, Carmen de la Pinta, Carolina Barreto Melian, Emma Rodríguez Garrote, Mercedes Carrato, Alfredo Ruiz-Cañas, Laura Sainz, Jr, Bruno Torres, Ana Smolkova, Bozena Earl, Julie |
description | Tumor organoids are three-dimensional (3D) ex vivo tumor models that recapitulate the biological key features of the original primary tumor tissues. Patient-derived tumor organoids have been used in translational cancer research and can be applied to assess treatment sensitivity and resistance, cell-cell interactions, and tumor cell interactions with the tumor microenvironment. Tumor organoids are complex culture systems that require advanced cell culture techniques and culture media with specific growth factor cocktails and a biological basement membrane that mimics the extracellular environment. The ability to establish primary tumor cultures highly depends on the tissue of origin, the cellularity, and the clinical features of the tumor, such as the tumor grade. Furthermore, tissue sample collection, material quality and quantity, as well as correct biobanking and storage are crucial elements of this procedure. The technical capabilities of the laboratory are also crucial factors to consider. Here, we report a validated SOP/protocol that is technically and economically feasible for the culture of ex vivo tumor organoids from fresh tissue samples of pancreatic adenocarcinoma origin, either from fresh primary resected patient donor tissue or patient-derived xenografts (PDX). The technique described herein can be performed in laboratories with basic tissue culture and mouse facilities and is tailored for wide application in the translational oncology field. |
doi_str_mv | 10.3791/65229 |
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Patient-derived tumor organoids have been used in translational cancer research and can be applied to assess treatment sensitivity and resistance, cell-cell interactions, and tumor cell interactions with the tumor microenvironment. Tumor organoids are complex culture systems that require advanced cell culture techniques and culture media with specific growth factor cocktails and a biological basement membrane that mimics the extracellular environment. The ability to establish primary tumor cultures highly depends on the tissue of origin, the cellularity, and the clinical features of the tumor, such as the tumor grade. Furthermore, tissue sample collection, material quality and quantity, as well as correct biobanking and storage are crucial elements of this procedure. The technical capabilities of the laboratory are also crucial factors to consider. Here, we report a validated SOP/protocol that is technically and economically feasible for the culture of ex vivo tumor organoids from fresh tissue samples of pancreatic adenocarcinoma origin, either from fresh primary resected patient donor tissue or patient-derived xenografts (PDX). The technique described herein can be performed in laboratories with basic tissue culture and mouse facilities and is tailored for wide application in the translational oncology field.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/65229</identifier><identifier>PMID: 37306424</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma ; Animals ; Biological Specimen Banks ; Fibroblasts ; Humans ; Mice ; Organoids ; Pancreatic Neoplasms ; Tumor Microenvironment</subject><ispartof>Journal of visualized experiments, 2023-05 (195)</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3830,27901,27902</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.3791/65229$$EView_record_in_Journal_of_Visualized_Experiments$$FView_record_in_$$GJournal_of_Visualized_Experiments</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37306424$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Díaz-Alejo, Jesús Frutos</creatorcontrib><creatorcontrib>April-Monn, Simon</creatorcontrib><creatorcontrib>Cihova, Marina</creatorcontrib><creatorcontrib>Buocikova, Verona</creatorcontrib><creatorcontrib>Villalón López, Jorge</creatorcontrib><creatorcontrib>Urbanova, Maria</creatorcontrib><creatorcontrib>Lechuga, Carmen G</creatorcontrib><creatorcontrib>Tomas, Miroslav</creatorcontrib><creatorcontrib>Dubovan, Peter</creatorcontrib><creatorcontrib>Sánchez, Bárbara Luna</creatorcontrib><creatorcontrib>Páez, Sonia Camaño</creatorcontrib><creatorcontrib>Sanjuanbenito, Alfonso</creatorcontrib><creatorcontrib>Lobo, Eduardo</creatorcontrib><creatorcontrib>Romio de la Heras, Estefanía</creatorcontrib><creatorcontrib>Guerra, Carmen</creatorcontrib><creatorcontrib>de la Pinta, Carolina</creatorcontrib><creatorcontrib>Barreto Melian, Emma</creatorcontrib><creatorcontrib>Rodríguez Garrote, Mercedes</creatorcontrib><creatorcontrib>Carrato, Alfredo</creatorcontrib><creatorcontrib>Ruiz-Cañas, Laura</creatorcontrib><creatorcontrib>Sainz, Jr, Bruno</creatorcontrib><creatorcontrib>Torres, Ana</creatorcontrib><creatorcontrib>Smolkova, Bozena</creatorcontrib><creatorcontrib>Earl, Julie</creatorcontrib><title>Establishment of Pancreatic Cancer-Derived Tumor Organoids and Fibroblasts From Fresh Tissue</title><title>Journal of visualized experiments</title><addtitle>J Vis Exp</addtitle><description>Tumor organoids are three-dimensional (3D) ex vivo tumor models that recapitulate the biological key features of the original primary tumor tissues. Patient-derived tumor organoids have been used in translational cancer research and can be applied to assess treatment sensitivity and resistance, cell-cell interactions, and tumor cell interactions with the tumor microenvironment. Tumor organoids are complex culture systems that require advanced cell culture techniques and culture media with specific growth factor cocktails and a biological basement membrane that mimics the extracellular environment. The ability to establish primary tumor cultures highly depends on the tissue of origin, the cellularity, and the clinical features of the tumor, such as the tumor grade. Furthermore, tissue sample collection, material quality and quantity, as well as correct biobanking and storage are crucial elements of this procedure. The technical capabilities of the laboratory are also crucial factors to consider. Here, we report a validated SOP/protocol that is technically and economically feasible for the culture of ex vivo tumor organoids from fresh tissue samples of pancreatic adenocarcinoma origin, either from fresh primary resected patient donor tissue or patient-derived xenografts (PDX). The technique described herein can be performed in laboratories with basic tissue culture and mouse facilities and is tailored for wide application in the translational oncology field.</description><subject>Adenocarcinoma</subject><subject>Animals</subject><subject>Biological Specimen Banks</subject><subject>Fibroblasts</subject><subject>Humans</subject><subject>Mice</subject><subject>Organoids</subject><subject>Pancreatic Neoplasms</subject><subject>Tumor Microenvironment</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEFLwzAYhoMobs79BclF8FJNvmRNe5S5qSDMwwQPQkmTry7SNjNpBf-91U3x8r7v4eE9PIRMObsUKudX6QwgPyBjnkuWsEw9H_7bI3IS4xtjKbBZdkxGQgmWSpBj8rKInS5rFzcNth31FX3UrQmoO2fofJgYkhsM7gMtXfeND3QVXnXrnY1Ut5YuXRl8WevYRboMvhkC44auXYw9npKjStcRp_uekKflYj2_Sx5Wt_fz64fEgORdIjgHKUErIzMARIYmk5XWHK0ywDkTxloGBvNcZshTqJQFzjikqswFMjEhF7vfbfDvPcauaFw0WNe6Rd_HAjKY8ZlUIh_Q8x1qgo8xYFVsg2t0-Cw4K75FFj8iB-5sf9mXDdo_6tec-AIYemxm</recordid><startdate>20230526</startdate><enddate>20230526</enddate><creator>Díaz-Alejo, Jesús Frutos</creator><creator>April-Monn, Simon</creator><creator>Cihova, Marina</creator><creator>Buocikova, Verona</creator><creator>Villalón López, Jorge</creator><creator>Urbanova, Maria</creator><creator>Lechuga, Carmen G</creator><creator>Tomas, Miroslav</creator><creator>Dubovan, Peter</creator><creator>Sánchez, Bárbara Luna</creator><creator>Páez, Sonia Camaño</creator><creator>Sanjuanbenito, Alfonso</creator><creator>Lobo, Eduardo</creator><creator>Romio de la Heras, Estefanía</creator><creator>Guerra, Carmen</creator><creator>de la Pinta, Carolina</creator><creator>Barreto Melian, Emma</creator><creator>Rodríguez Garrote, Mercedes</creator><creator>Carrato, Alfredo</creator><creator>Ruiz-Cañas, Laura</creator><creator>Sainz, Jr, Bruno</creator><creator>Torres, Ana</creator><creator>Smolkova, Bozena</creator><creator>Earl, Julie</creator><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></search><sort><creationdate>20230526</creationdate><title>Establishment of Pancreatic Cancer-Derived Tumor Organoids and Fibroblasts From Fresh Tissue</title><author>Díaz-Alejo, Jesús Frutos ; 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Patient-derived tumor organoids have been used in translational cancer research and can be applied to assess treatment sensitivity and resistance, cell-cell interactions, and tumor cell interactions with the tumor microenvironment. Tumor organoids are complex culture systems that require advanced cell culture techniques and culture media with specific growth factor cocktails and a biological basement membrane that mimics the extracellular environment. The ability to establish primary tumor cultures highly depends on the tissue of origin, the cellularity, and the clinical features of the tumor, such as the tumor grade. Furthermore, tissue sample collection, material quality and quantity, as well as correct biobanking and storage are crucial elements of this procedure. The technical capabilities of the laboratory are also crucial factors to consider. Here, we report a validated SOP/protocol that is technically and economically feasible for the culture of ex vivo tumor organoids from fresh tissue samples of pancreatic adenocarcinoma origin, either from fresh primary resected patient donor tissue or patient-derived xenografts (PDX). The technique described herein can be performed in laboratories with basic tissue culture and mouse facilities and is tailored for wide application in the translational oncology field.</abstract><cop>United States</cop><pmid>37306424</pmid><doi>10.3791/65229</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Animals Biological Specimen Banks Fibroblasts Humans Mice Organoids Pancreatic Neoplasms Tumor Microenvironment |
title | Establishment of Pancreatic Cancer-Derived Tumor Organoids and Fibroblasts From Fresh Tissue |
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