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A bioprinted human-glioblastoma-on-a-chip for the identification of patient-specific responses to chemoradiotherapy.
Yi, Hee-Gyeong; Jeong, Young Hun; Kim, Yona; Choi, Yeong-Jin; Moon, Hyo Eun; Park, Sung Hye; Kang, Kyung Shin; Bae, Mihyeon; Jang, Jinah; Youn, Hyewon; Paek, Sun Ha; Cho, Dong-Woo.
Afiliação
  • Yi HG; Department of Mechanical Engineering, POSTECH, Pohang, Korea.
  • Jeong YH; School of Mechanical Engineering, Kyungpook National University, Daegu, Korea.
  • Kim Y; Department of Neurosurgery, Cancer Research Institute and Ischemic/Hypoxic Disease Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Choi YJ; Division of Integrative Biosciences and Biotechnology, POSTECH, Pohang, Korea.
  • Moon HE; Powder & Ceramics Division, Korea Institute of Materials Science, Changwon, Korea.
  • Park SH; Department of Neurosurgery, Cancer Research Institute and Ischemic/Hypoxic Disease Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Kang KS; Department of Pathology, Seoul National University College of Medicine, Seoul, Korea.
  • Bae M; School of Physical Sciences and Engineering, Anderson University, Anderson, IN, USA.
  • Jang J; Department of Mechanical Engineering, POSTECH, Pohang, Korea.
  • Youn H; Department of Creative IT Engineering, POSTECH, Pohang, Korea.
  • Paek SH; School of Interdisciplinary Bioscience and Bioengineering, POSTECH, Pohang, Korea.
  • Cho DW; Department of Nuclear Medicine and Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Nat Biomed Eng ; 3(7): 509-519, 2019 07.
Article em En | MEDLINE | ID: mdl-31148598
Patient-specific ex vivo models of human tumours that recapitulate the pathological characteristics and complex ecology of native tumours could help determine the most appropriate cancer treatment for individual patients. Here, we show that bioprinted reconstituted glioblastoma tumours consisting of patient-derived tumour cells, vascular endothelial cells and decellularized extracellular matrix from brain tissue in a compartmentalized cancer-stroma concentric-ring structure that sustains a radial oxygen gradient, recapitulate the structural, biochemical and biophysical properties of the native tumours. We also show that the glioblastoma-on-a-chip reproduces clinically observed patient-specific resistances to treatment with concurrent chemoradiation and temozolomide, and that the model can be used to determine drug combinations associated with superior tumour killing. The patient-specific tumour-on-a-chip model might be useful for the identification of effective treatments for glioblastoma patients resistant to the standard first-line treatment.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma / Dispositivos Lab-On-A-Chip / Quimiorradioterapia / Bioimpressão Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Nat Biomed Eng Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma / Dispositivos Lab-On-A-Chip / Quimiorradioterapia / Bioimpressão Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Nat Biomed Eng Ano de publicação: 2019 Tipo de documento: Article