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Engineering a High-Throughput 3-D In Vitro Glioblastoma Model

机译:设计高通量3D体外胶质母细胞瘤模型

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摘要

Glioblastoma multiforme (GBM) is the most common and malignant primary brain tumor in adults because of its highly invasive behavior. The existing treatment for GBM, which involves a combination of resection, chemotherapy, and radiotherapy, has a very limited success rate with a median survival rate of <1 year. This is mainly because of the failure of early detection and effective treatment. We designed a novel 3-D GBM cell culture model based on microwells that could mimic in vitro environment and help to bypass the lack of suitable animal models for preclinical toxicity tests. Microwells were fabricated from simple and inexpensive polyethylene glycol material for the control of in vitro 3-D culture. We applied the 3-D micropatterning system to GBM (U-87) cells using the photolithography technique to control the cell spheroids’ shape, size, and thickness. Our preliminary results suggested that uniform GBM spheroids can be formed in 3-D, and the size of these GBM spheroids depends on the size of microwells. The viability of the spheroids generated in this manner was quantitatively evaluated using live/dead assay and shown to improve over 21 days. We believe that in vitro 3-D cell culture model could help to reduce the time of the preclinical brain tumor growth studies. The proposed novel platform could be useful and cost-effective for high-throughput screening of cancer drugs and assessment of treatment responses.
机译:多形性胶质母细胞瘤(GBM)是成年人中最常见,最恶性的原发性脑肿瘤,因为它具有高度侵袭性。 GBM的现有治疗包括切除,化学疗法和放射疗法的结合,成功率非常有限,中位生存期不到1年。这主要是由于早期检测和有效治疗的失败。我们设计了一种基于微孔的新型3-D GBM细胞培养模型,该模型可以模拟体外环境,并有助于绕开缺乏合适的动物模型进行临床前毒性测试的过程。微孔由简单且便宜的聚乙二醇材料制成,用于控制体外3-D培养。我们使用光刻技术将3-D微图案化系统应用于GBM(U-87)细胞,以控制细胞球体的形状,大小和厚度。我们的初步结果表明,可以在3-D中形成均匀的GBM球状体,这些GBM球状体的大小取决于微孔的大小。使用活/死分析定量评估以此方式产生的球体的生存力,并显示在21天内有所改善。我们相信,体外3-D细胞培养模型可以帮助减少临床前脑肿瘤生长研究的时间。拟议的新型平台对于癌症药物的高通量筛选和治疗反应评估可能是有用且具有成本效益的。

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