Breast Cancer Organoids Model Patient-Specific Response to Drug Treatment.
Elena CampanerAlessandro ZanniniMariangela SantorsolaDeborah BonazzaCristina BottinValeria CancilaClaudio TripodoMarina BortulFabrizio ZanconatiStefan SchoeftnerGiannino Del SalPublished in: Cancers (2020)
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.
Keyphrases
- drug resistant
- multidrug resistant
- epidermal growth factor receptor
- acinetobacter baumannii
- induced pluripotent stem cells
- single cell
- tyrosine kinase
- emergency department
- pseudomonas aeruginosa
- ejection fraction
- stem cells
- lymph node
- prognostic factors
- gene expression
- end stage renal disease
- genome wide
- advanced non small cell lung cancer
- patient reported outcomes
- mesenchymal stem cells
- bone marrow
- copy number
- combination therapy
- drug induced
- lymph node metastasis