| Literature DB >> 33371412 |
Elena Campaner1,2, Alessandro Zannini1,2, Mariangela Santorsola1,2, Deborah Bonazza3,4, Cristina Bottin3,4, Valeria Cancila5, Claudio Tripodo5,6, Marina Bortul3,7, Fabrizio Zanconati3,4, Stefan Schoeftner1,2, Giannino Del Sal1,2,6.
Abstract
Tumor organoids are tridimensional cell culture systems that are generated in vitro from surgically resected patients' tumors. They can be propagated in culture maintaining several features of the tumor of origin, including cellular and genetic heterogeneity, thus representing a promising tool for precision cancer medicine. Here, we established patient-derived tumor organoids (PDOs) from different breast cancer subtypes (luminal A, luminal B, human epidermal growth factor receptor 2 (HER2)-enriched, and triple negative). The established model systems showed histological and genomic concordance with parental tumors. However, in PDOs, the ratio of diverse cell populations was frequently different from that originally observed in parental tumors. We showed that tumor organoids represent a valuable system to test the efficacy of standard therapeutic treatments and to identify drug resistant populations within tumors. We also report that inhibitors of mechanosignaling and of Yes-associated protein 1 (YAP) activation can restore chemosensitivity in drug resistant tumor organoids.Entities:
Keywords: YAP; breast cancer; dasatinib; drug testing; heterogeneity; mechanotransduction; patient-derived tumor organoids; statin
Year: 2020 PMID: 33371412 PMCID: PMC7770601 DOI: 10.3390/cancers12123869
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639