球体
细胞病理学
体外
顺铂
活力测定
生物物理学
化学
生物医学工程
生物
病理
化疗
医学
生物化学
遗传学
作者
Shreya Raghavan,Pooja Mehta,Eric N. Horst,Maria R. Ward,Katelyn R. Rowley,Geeta Mehta
出处
期刊:Oncotarget
[Impact Journals, LLC]
日期:2016-02-24
卷期号:7 (13): 16948-16961
被引量:102
标识
DOI:10.18632/oncotarget.7659
摘要
Multicellular tumor spheroids are powerful in vitro models to perform preclinical chemosensitivity assays. We compare different methodologies to generate tumor spheroids in terms of resultant spheroid morphology, cellular arrangement and chemosensitivity. We used two cancer cell lines (MCF7 and OVCAR8) to generate spheroids using i) hanging drop array plates; ii) liquid overlay on ultra-low attachment plates; iii) liquid overlay on ultra-low attachment plates with rotating mixing (nutator plates). Analysis of spheroid morphometry indicated that cellular compaction was increased in spheroids generated on nutator and hanging drop array plates. Collagen staining also indicated higher compaction and remodeling in tumor spheroids on nutator and hanging drop arrays compared to conventional liquid overlay. Consequently, spheroids generated on nutator or hanging drop plates had increased chemoresistance to cisplatin treatment (20-60% viability) compared to spheroids on ultra low attachment plates (10-20% viability). Lastly, we used a mathematical model to demonstrate minimal changes in oxygen and cisplatin diffusion within experimentally generated spheroids. Our results demonstrate that in vitro methods of tumor spheroid generation result in varied cellular arrangement and chemosensitivity.
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