替莫唑胺
放化疗
离体
癌症研究
胶质瘤
癌症
U87型
胶质母细胞瘤
细胞外基质
医学
病理
体内
生物
内科学
细胞生物学
生物技术
作者
Hee‐Gyeong Yi,Young Hun Jeong,Yona Kim,Yeong‐Jin Choi,Hyo Eun Moon,Sung‐Hye Park,Kyung Shin Kang,Mihyeon Bae,Jinah Jang,Hyewon Youn,Sun Ha Paek,Dong‐Woo Cho
标识
DOI:10.1038/s41551-019-0363-x
摘要
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. A tumour-on-a-chip model featuring patient-derived glioblastoma cells, vascular endothelial cells and decellularized extracellular matrix from brain tissue can be used to identify patient-specific resistance to standard chemoradiotherapy.
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