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BRCA-deficient mouse mammary tumor organoids to study cancer-drug resistance.

Alexandra A DuarteEwa GogolaNorman SachsMarco BarazasStefano AnnunziatoJulian R de RuiterArno VeldsSohvi BlatterJulia M HouthuijzenMarieke van de VenHans CleversPiet BorstJos JonkersSven Rottenberg
Published in: Nature methods (2017)
Poly(ADP-ribose) polymerase inhibition (PARPi) is a promising new therapeutic approach for the treatment of cancers that show homologous recombination deficiency (HRD). Despite the success of PARPi in targeting HRD in tumors that lack the tumor suppressor function of BRCA1 or BRCA2, drug resistance poses a major obstacle. We developed three-dimensional cancer organoids derived from genetically engineered mouse models (GEMMs) for BRCA1- and BRCA2-deficient cancers. Unlike conventional cell lines or mammospheres, organoid cultures can be efficiently derived and rapidly expanded in vitro. Orthotopically transplanted organoids give rise to mammary tumors that recapitulate the epithelial morphology and preserve the drug response of the original tumor. Notably, GEMM-tumor-derived organoids can be easily genetically modified, making them a powerful tool for genetic studies of tumor biology and drug resistance.
Keyphrases
  • papillary thyroid
  • dna damage
  • mouse model
  • emergency department
  • squamous cell
  • dna repair
  • induced pluripotent stem cells
  • drug delivery
  • dna methylation
  • genome wide
  • cancer therapy
  • childhood cancer