Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours

BMC Cancer. 2019 Oct 21;19(1):970. doi: 10.1186/s12885-019-6149-4.

Abstract

Background: Neuroblastoma (NB) is a paediatric tumour of the sympathetic nervous system. Half of all cases are defined high-risk with an overall survival less than 40% at 5 years from diagnosis. The lack of in vitro models able to recapitulate the intrinsic heterogeneity of primary NB tumours has hindered progress in understanding disease pathogenesis and therapy response.

Methods: Here we describe the establishment of 6 patient-derived organoids (PDOs) from cells of NB tumour biopsies capable of self-organising in a structure resembling the tissue of origin.

Results: PDOs recapitulate the histological architecture typical of the NB tumour. Moreover, PDOs expressed NB specific markers such as neural cell adhesion molecules, NB84 antigen, synaptophysin (SYP), chromogranin A (CHGA) and neural cell adhesion molecule NCAM (CD56). Analyses of whole genome genotyping array revealed that PDOs maintained patient-specific chromosomal aberrations such as MYCN amplification, deletion of 1p and gain of chromosome 17q. Furthermore, the PDOs showed stemness features and retained cellular heterogeneity reflecting the high heterogeneity of NB tumours.

Conclusions: We were able to create a novel preclinical model for NB exhibiting self-renewal property and allowing to obtain a reservoir of NB patients' biological material useful for the study of NB molecular pathogenesis and to test drugs for personalised treatments.

Keywords: Neuroblastoma; Patient-derived organoids; Preclinical model.

MeSH terms

  • Autonomic Nervous System Diseases / genetics*
  • Autonomic Nervous System Diseases / metabolism
  • Autonomic Nervous System Diseases / pathology*
  • Biomarkers, Tumor / metabolism
  • Biopsy
  • Child
  • Child, Preschool
  • Chromogranin A / metabolism
  • Chromosome Aberrations
  • Gene Amplification / genetics
  • Humans
  • Infant
  • Models, Biological*
  • N-Myc Proto-Oncogene Protein / genetics
  • Neuroblastoma / genetics*
  • Neuroblastoma / metabolism
  • Neuroblastoma / pathology*
  • Organoids / metabolism
  • Organoids / pathology*
  • Receptors, G-Protein-Coupled / metabolism
  • Synaptophysin / metabolism

Substances

  • Biomarkers, Tumor
  • CHGA protein, human
  • Chromogranin A
  • LGR5 protein, human
  • MYCN protein, human
  • N-Myc Proto-Oncogene Protein
  • Receptors, G-Protein-Coupled
  • SYP protein, human
  • Synaptophysin