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Towards personalized induction therapy for esophageal adenocarcinoma: organoids derived from endoscopic biopsy recapitulate the pre-treatment tumor.
Derouet, Mathieu F; Allen, Jonathan; Wilson, Gavin W; Ng, Christine; Radulovich, Nikolina; Kalimuthu, Sangeetha; Tsao, Ming-Sound; Darling, Gail E; Yeung, Jonathan C.
Afiliação
  • Derouet MF; Latner Thoracic Surgery Research Laboratories, Princess Margaret Cancer Research Tower, University Health Network, Toronto, ON, Canada.
  • Allen J; Latner Thoracic Surgery Research Laboratories, Princess Margaret Cancer Research Tower, University Health Network, Toronto, ON, Canada.
  • Wilson GW; Latner Thoracic Surgery Research Laboratories, Princess Margaret Cancer Research Tower, University Health Network, Toronto, ON, Canada.
  • Ng C; Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
  • Radulovich N; Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
  • Kalimuthu S; Department of Pathology, University Health Network, Toronto, Canada.
  • Tsao MS; Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
  • Darling GE; Department of Pathology, University Health Network, Toronto, Canada.
  • Yeung JC; Latner Thoracic Surgery Research Laboratories, Princess Margaret Cancer Research Tower, University Health Network, Toronto, ON, Canada.
Sci Rep ; 10(1): 14514, 2020 09 03.
Article em En | MEDLINE | ID: mdl-32884042
ABSTRACT
Esophageal adenocarcinoma has few known recurrent mutations and therefore robust, reliable and reproducible patient-specific models are needed for personalized treatment. Patient-derived organoid culture is a strategy that may allow for the personalized study of esophageal adenocarcinoma and the development of personalized induction therapy. We therefore developed a protocol to establish EAC organoids from endoscopic biopsies of naïve esophageal adenocarcinomas. Histologic characterization and molecular characterization of organoids by whole exome sequencing demonstrated recapitulation of the tumors' histology and genomic (~ 60% SNV overlap) characteristics. Drug testing using clinically appropriate chemotherapeutics and targeted therapeutics showed an overlap between the patient's tumor response and the corresponding organoids' response. Furthermore, we identified Barrett's esophagus epithelium as a potential source of organoid culture contamination. In conclusion, organoids can be robustly cultured from endoscopic biopsies of esophageal adenocarcinoma and recapitulate the originating tumor. This model demonstrates promise as a tool to better personalize therapy for esophageal adenocarcinoma patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Adenocarcinoma / Medicina de Precisão / Quimioterapia de Indução Tipo de estudo: Guideline / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Adenocarcinoma / Medicina de Precisão / Quimioterapia de Indução Tipo de estudo: Guideline / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2020 Tipo de documento: Article