| Literature DB >> 31148598 |
Hee-Gyeong Yi1, Young Hun Jeong2, Yona Kim3, Yeong-Jin Choi4,5, Hyo Eun Moon3, Sung Hye Park6, Kyung Shin Kang7, Mihyeon Bae1, Jinah Jang8,9, Hyewon Youn10, Sun Ha Paek11, Dong-Woo Cho12.
Abstract
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.Entities:
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Year: 2019 PMID: 31148598 DOI: 10.1038/s41551-019-0363-x
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671