Cargando…

Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids

Patient-derived cancer organoids hold great potential to accurately model and predict therapeutic responses. Efficient organoid isolation methods that minimize post-collection manipulation of tissues would improve adaptability, accuracy, and applicability to both experimental and real-time clinical...

Descripción completa

Detalles Bibliográficos
Autores principales: Vilgelm, Anna E., Bergdorf, Kensey, Wolf, Melissa, Bharti, Vijaya, Shattuck-Brandt, Rebecca, Blevins, Ashlyn, Jones, Caroline, Phifer, Courtney, Lee, Mason, Lowe, Cindy, Hongo, Rachel, Boyd, Kelli, Netterville, James, Rohde, Sarah, Idrees, Kamran, Bauer, Joshua A., Westover, David, Reinfeld, Bradley, Baregamian, Naira, Richmond, Ann, Rathmell, W. Kimryn, Lee, Ethan, McDonald, Oliver G., Weiss, Vivian L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415927/
https://www.ncbi.nlm.nih.gov/pubmed/32771978
http://dx.doi.org/10.1016/j.isci.2020.101408
_version_ 1783569231096315904
author Vilgelm, Anna E.
Bergdorf, Kensey
Wolf, Melissa
Bharti, Vijaya
Shattuck-Brandt, Rebecca
Blevins, Ashlyn
Jones, Caroline
Phifer, Courtney
Lee, Mason
Lowe, Cindy
Hongo, Rachel
Boyd, Kelli
Netterville, James
Rohde, Sarah
Idrees, Kamran
Bauer, Joshua A.
Westover, David
Reinfeld, Bradley
Baregamian, Naira
Richmond, Ann
Rathmell, W. Kimryn
Lee, Ethan
McDonald, Oliver G.
Weiss, Vivian L.
author_facet Vilgelm, Anna E.
Bergdorf, Kensey
Wolf, Melissa
Bharti, Vijaya
Shattuck-Brandt, Rebecca
Blevins, Ashlyn
Jones, Caroline
Phifer, Courtney
Lee, Mason
Lowe, Cindy
Hongo, Rachel
Boyd, Kelli
Netterville, James
Rohde, Sarah
Idrees, Kamran
Bauer, Joshua A.
Westover, David
Reinfeld, Bradley
Baregamian, Naira
Richmond, Ann
Rathmell, W. Kimryn
Lee, Ethan
McDonald, Oliver G.
Weiss, Vivian L.
author_sort Vilgelm, Anna E.
collection PubMed
description Patient-derived cancer organoids hold great potential to accurately model and predict therapeutic responses. Efficient organoid isolation methods that minimize post-collection manipulation of tissues would improve adaptability, accuracy, and applicability to both experimental and real-time clinical settings. Here we present a simple and minimally invasive fine-needle aspiration (FNA)-based organoid culture technique using a variety of tumor types including gastrointestinal, thyroid, melanoma, and kidney. This method isolates organoids directly from patients at the bedside or from resected tissues, requiring minimal tissue processing while preserving the histologic growth patterns and infiltrating immune cells. Finally, we illustrate diverse downstream applications of this technique including in vitro high-throughput chemotherapeutic screens, in situ immune cell characterization, and in vivo patient-derived xenografts. Thus, routine clinical FNA-based collection techniques represent an unappreciated substantial source of material that can be exploited to generate tumor organoids from a variety of tumor types for both discovery and clinical applications.
format Online
Article
Text
id pubmed-7415927
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-74159272020-08-12 Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids Vilgelm, Anna E. Bergdorf, Kensey Wolf, Melissa Bharti, Vijaya Shattuck-Brandt, Rebecca Blevins, Ashlyn Jones, Caroline Phifer, Courtney Lee, Mason Lowe, Cindy Hongo, Rachel Boyd, Kelli Netterville, James Rohde, Sarah Idrees, Kamran Bauer, Joshua A. Westover, David Reinfeld, Bradley Baregamian, Naira Richmond, Ann Rathmell, W. Kimryn Lee, Ethan McDonald, Oliver G. Weiss, Vivian L. iScience Article Patient-derived cancer organoids hold great potential to accurately model and predict therapeutic responses. Efficient organoid isolation methods that minimize post-collection manipulation of tissues would improve adaptability, accuracy, and applicability to both experimental and real-time clinical settings. Here we present a simple and minimally invasive fine-needle aspiration (FNA)-based organoid culture technique using a variety of tumor types including gastrointestinal, thyroid, melanoma, and kidney. This method isolates organoids directly from patients at the bedside or from resected tissues, requiring minimal tissue processing while preserving the histologic growth patterns and infiltrating immune cells. Finally, we illustrate diverse downstream applications of this technique including in vitro high-throughput chemotherapeutic screens, in situ immune cell characterization, and in vivo patient-derived xenografts. Thus, routine clinical FNA-based collection techniques represent an unappreciated substantial source of material that can be exploited to generate tumor organoids from a variety of tumor types for both discovery and clinical applications. Elsevier 2020-07-24 /pmc/articles/PMC7415927/ /pubmed/32771978 http://dx.doi.org/10.1016/j.isci.2020.101408 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Vilgelm, Anna E.
Bergdorf, Kensey
Wolf, Melissa
Bharti, Vijaya
Shattuck-Brandt, Rebecca
Blevins, Ashlyn
Jones, Caroline
Phifer, Courtney
Lee, Mason
Lowe, Cindy
Hongo, Rachel
Boyd, Kelli
Netterville, James
Rohde, Sarah
Idrees, Kamran
Bauer, Joshua A.
Westover, David
Reinfeld, Bradley
Baregamian, Naira
Richmond, Ann
Rathmell, W. Kimryn
Lee, Ethan
McDonald, Oliver G.
Weiss, Vivian L.
Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids
title Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids
title_full Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids
title_fullStr Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids
title_full_unstemmed Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids
title_short Fine-Needle Aspiration-Based Patient-Derived Cancer Organoids
title_sort fine-needle aspiration-based patient-derived cancer organoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415927/
https://www.ncbi.nlm.nih.gov/pubmed/32771978
http://dx.doi.org/10.1016/j.isci.2020.101408
work_keys_str_mv AT vilgelmannae fineneedleaspirationbasedpatientderivedcancerorganoids
AT bergdorfkensey fineneedleaspirationbasedpatientderivedcancerorganoids
AT wolfmelissa fineneedleaspirationbasedpatientderivedcancerorganoids
AT bhartivijaya fineneedleaspirationbasedpatientderivedcancerorganoids
AT shattuckbrandtrebecca fineneedleaspirationbasedpatientderivedcancerorganoids
AT blevinsashlyn fineneedleaspirationbasedpatientderivedcancerorganoids
AT jonescaroline fineneedleaspirationbasedpatientderivedcancerorganoids
AT phifercourtney fineneedleaspirationbasedpatientderivedcancerorganoids
AT leemason fineneedleaspirationbasedpatientderivedcancerorganoids
AT lowecindy fineneedleaspirationbasedpatientderivedcancerorganoids
AT hongorachel fineneedleaspirationbasedpatientderivedcancerorganoids
AT boydkelli fineneedleaspirationbasedpatientderivedcancerorganoids
AT nettervillejames fineneedleaspirationbasedpatientderivedcancerorganoids
AT rohdesarah fineneedleaspirationbasedpatientderivedcancerorganoids
AT idreeskamran fineneedleaspirationbasedpatientderivedcancerorganoids
AT bauerjoshuaa fineneedleaspirationbasedpatientderivedcancerorganoids
AT westoverdavid fineneedleaspirationbasedpatientderivedcancerorganoids
AT reinfeldbradley fineneedleaspirationbasedpatientderivedcancerorganoids
AT baregamiannaira fineneedleaspirationbasedpatientderivedcancerorganoids
AT richmondann fineneedleaspirationbasedpatientderivedcancerorganoids
AT rathmellwkimryn fineneedleaspirationbasedpatientderivedcancerorganoids
AT leeethan fineneedleaspirationbasedpatientderivedcancerorganoids
AT mcdonaldoliverg fineneedleaspirationbasedpatientderivedcancerorganoids
AT weissvivianl fineneedleaspirationbasedpatientderivedcancerorganoids