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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases

The pressure towards innovation and creation of new model systems in regenerative medicine and cancer research has fostered the development of novel potential therapeutic applications. Kidney injuries provoke a high request of organ transplants making it the most demanding system in the field of reg...

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Autores principales: Grassi, Ludovica, Alfonsi, Romina, Francescangeli, Federica, Signore, Michele, De Angelis, Maria Laura, Addario, Antonio, Costantini, Manuela, Flex, Elisabetta, Ciolfi, Andrea, Pizzi, Simone, Bruselles, Alessandro, Pallocca, Matteo, Simone, Giuseppe, Haoui, Mustapha, Falchi, Mario, Milella, Michele, Sentinelli, Steno, Di Matteo, Paola, Stellacci, Emilia, Gallucci, Michele, Muto, Giovanni, Tartaglia, Marco, De Maria, Ruggero, Bonci, Désirée
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393468/
https://www.ncbi.nlm.nih.gov/pubmed/30814510
http://dx.doi.org/10.1038/s41419-019-1453-0
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author Grassi, Ludovica
Alfonsi, Romina
Francescangeli, Federica
Signore, Michele
De Angelis, Maria Laura
Addario, Antonio
Costantini, Manuela
Flex, Elisabetta
Ciolfi, Andrea
Pizzi, Simone
Bruselles, Alessandro
Pallocca, Matteo
Simone, Giuseppe
Haoui, Mustapha
Falchi, Mario
Milella, Michele
Sentinelli, Steno
Di Matteo, Paola
Stellacci, Emilia
Gallucci, Michele
Muto, Giovanni
Tartaglia, Marco
De Maria, Ruggero
Bonci, Désirée
author_facet Grassi, Ludovica
Alfonsi, Romina
Francescangeli, Federica
Signore, Michele
De Angelis, Maria Laura
Addario, Antonio
Costantini, Manuela
Flex, Elisabetta
Ciolfi, Andrea
Pizzi, Simone
Bruselles, Alessandro
Pallocca, Matteo
Simone, Giuseppe
Haoui, Mustapha
Falchi, Mario
Milella, Michele
Sentinelli, Steno
Di Matteo, Paola
Stellacci, Emilia
Gallucci, Michele
Muto, Giovanni
Tartaglia, Marco
De Maria, Ruggero
Bonci, Désirée
author_sort Grassi, Ludovica
collection PubMed
description The pressure towards innovation and creation of new model systems in regenerative medicine and cancer research has fostered the development of novel potential therapeutic applications. Kidney injuries provoke a high request of organ transplants making it the most demanding system in the field of regenerative medicine. Furthermore, renal cancer frequently threaten patients’ life and aggressive forms still remain difficult to treat. Ethical issues related to the use of embryonic stem cells, has fueled research on adult, patient-specific pluripotent stem cells as a model for discovery and therapeutic development, but to date, normal and cancerous renal experimental models are lacking. Several research groups are focusing on the development of organoid cultures. Since organoids mimic the original tissue architecture in vitro, they represent an excellent model for tissue engineering studies and cancer therapy testing. We established normal and tumor renal cell carcinoma organoids previously maintained in a heterogeneous multi-clone stem cell-like enriching medium. Starting from adult normal kidney specimens, we were able to isolate and propagate organoid 3D-structures composed of both differentiated and undifferentiated cells while expressing nephron specific markers. Furthermore, we were capable to establish organoids derived from cancer tissues although with a success rate inferior to that of their normal counterpart. Cancer cultures displayed epithelial and mesenchymal phenotype while retaining tumor specific markers. Of note, tumor organoids recapitulated neoplastic masses when orthotopically injected into immunocompromised mice. Our data suggest an innovative approach of long-term establishment of normal- and cancer-derived renal organoids obtained from cultures of fleshly dissociated adult tissues. Our results pave the way to organ replacement pioneering strategies as well as to new models for studying drug-induced nephrotoxicity and renal diseases. Along similar lines, deriving organoids from renal cancer patients opens unprecedented opportunities for generation of preclinical models aimed at improving therapeutic treatments.
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spelling pubmed-63934682019-02-28 Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases Grassi, Ludovica Alfonsi, Romina Francescangeli, Federica Signore, Michele De Angelis, Maria Laura Addario, Antonio Costantini, Manuela Flex, Elisabetta Ciolfi, Andrea Pizzi, Simone Bruselles, Alessandro Pallocca, Matteo Simone, Giuseppe Haoui, Mustapha Falchi, Mario Milella, Michele Sentinelli, Steno Di Matteo, Paola Stellacci, Emilia Gallucci, Michele Muto, Giovanni Tartaglia, Marco De Maria, Ruggero Bonci, Désirée Cell Death Dis Article The pressure towards innovation and creation of new model systems in regenerative medicine and cancer research has fostered the development of novel potential therapeutic applications. Kidney injuries provoke a high request of organ transplants making it the most demanding system in the field of regenerative medicine. Furthermore, renal cancer frequently threaten patients’ life and aggressive forms still remain difficult to treat. Ethical issues related to the use of embryonic stem cells, has fueled research on adult, patient-specific pluripotent stem cells as a model for discovery and therapeutic development, but to date, normal and cancerous renal experimental models are lacking. Several research groups are focusing on the development of organoid cultures. Since organoids mimic the original tissue architecture in vitro, they represent an excellent model for tissue engineering studies and cancer therapy testing. We established normal and tumor renal cell carcinoma organoids previously maintained in a heterogeneous multi-clone stem cell-like enriching medium. Starting from adult normal kidney specimens, we were able to isolate and propagate organoid 3D-structures composed of both differentiated and undifferentiated cells while expressing nephron specific markers. Furthermore, we were capable to establish organoids derived from cancer tissues although with a success rate inferior to that of their normal counterpart. Cancer cultures displayed epithelial and mesenchymal phenotype while retaining tumor specific markers. Of note, tumor organoids recapitulated neoplastic masses when orthotopically injected into immunocompromised mice. Our data suggest an innovative approach of long-term establishment of normal- and cancer-derived renal organoids obtained from cultures of fleshly dissociated adult tissues. Our results pave the way to organ replacement pioneering strategies as well as to new models for studying drug-induced nephrotoxicity and renal diseases. Along similar lines, deriving organoids from renal cancer patients opens unprecedented opportunities for generation of preclinical models aimed at improving therapeutic treatments. Nature Publishing Group UK 2019-02-27 /pmc/articles/PMC6393468/ /pubmed/30814510 http://dx.doi.org/10.1038/s41419-019-1453-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Grassi, Ludovica
Alfonsi, Romina
Francescangeli, Federica
Signore, Michele
De Angelis, Maria Laura
Addario, Antonio
Costantini, Manuela
Flex, Elisabetta
Ciolfi, Andrea
Pizzi, Simone
Bruselles, Alessandro
Pallocca, Matteo
Simone, Giuseppe
Haoui, Mustapha
Falchi, Mario
Milella, Michele
Sentinelli, Steno
Di Matteo, Paola
Stellacci, Emilia
Gallucci, Michele
Muto, Giovanni
Tartaglia, Marco
De Maria, Ruggero
Bonci, Désirée
Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
title Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
title_full Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
title_fullStr Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
title_full_unstemmed Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
title_short Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
title_sort organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393468/
https://www.ncbi.nlm.nih.gov/pubmed/30814510
http://dx.doi.org/10.1038/s41419-019-1453-0
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