TY - JOUR
T1 - Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
AU - Grassi, Ludovica
AU - Alfonsi, Romina
AU - Francescangeli, Federica
AU - Signore, Michele
AU - De Angelis, Maria Laura
AU - Addario, Antonio
AU - Costantini, Manuela
AU - Flex, Elisabetta
AU - Ciolfi, Andrea
AU - Pizzi, Simone
AU - Bruselles, Alessandro
AU - Pallocca, Matteo
AU - Simone, Giuseppe
AU - Haoui, Mustapha
AU - Falchi, Mario
AU - Milella, Michele
AU - Sentinelli, Steno
AU - Di Matteo, Paola
AU - Stellacci, Emilia
AU - Gallucci, Michele
AU - Muto, Giovanni
AU - Tartaglia, Marco
AU - De Maria Marchiano, Ruggero
AU - Bonci, Désirée
PY - 2019
Y1 - 2019
N2 - 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.
AB - 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.
KW - Cancer Research
KW - Cell Biology
KW - Cellular and Molecular Neuroscience
KW - Immunology
KW - Cancer Research
KW - Cell Biology
KW - Cellular and Molecular Neuroscience
KW - Immunology
UR - http://hdl.handle.net/10807/132788
UR - http://www.nature.com/cddis/marketing/index.html
U2 - 10.1038/s41419-019-1453-0
DO - 10.1038/s41419-019-1453-0
M3 - Article
SN - 2041-4889
VL - 10
SP - N/A-N/A
JO - CELL DEATH & DISEASE
JF - CELL DEATH & DISEASE
ER -