Tailoring esophageal tumor spheroids on a chip with inverse opal scaffolds for drug screening

Ruolin Shi, X. Wu, Yuanji Zhao, Shegan Gao, Gaofeng Liang
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Abstract

Esophageal cancer (EC) is characterized by high morbidity and mortality, and chemotherapy has become an indispensable means for comprehensive treatment. However, due to the limitation of the effective in vitro disease model, the development of chemotherapeutic agents still faces great challenges. In this paper, we present a novel tumor spheroid on a chip platform based on inverse opal hydrogel scaffolds to screen chemotherapeutic agents for EC treatment. With the microfluidic emulsion approach, the inverse opal hydrogel scaffolds were generated with tunable and organized pores, which could provide spatial confinement for cell growth. Thus, the suspended KYSE-70 cells could successfully form uniform cell spheroids on the inverse opal hydrogel scaffolds. It was demonstrated that the tumor cell spheroids could recapitulate 3D growth patterns in vivo and exhibited higher sensitivity to the chemotherapy agents compared with monolayer cells. Besides, by employing the scaffolds into a microfluidics to construct esophageal tumor on a chip, the device could realize high-throughput tumor cell spheroids generation and drug screening, indicating its promising role in chemotherapy drug development.
利用反蛋白石支架在芯片上定制食管肿瘤球体以进行药物筛选
食管癌(EC)具有高发病率和高死亡率的特点,化疗已成为综合治疗不可或缺的手段。然而,由于有效体外疾病模型的局限性,化疗药物的研发仍面临巨大挑战。本文提出了一种基于反蛋白水凝胶支架的新型肿瘤球形芯片平台,用于筛选治疗心肌梗死的化疗药物。通过微流控乳液方法,逆蛋白石水凝胶支架被制成具有可调且有组织的孔,可为细胞生长提供空间限制。因此,悬浮的 KYSE-70 细胞可以成功地在反蛋白石水凝胶支架上形成均匀的细胞球。实验证明,与单层细胞相比,肿瘤细胞球体能再现体内的三维生长模式,并表现出对化疗药物更高的敏感性。此外,将该支架应用于微流控芯片构建食管肿瘤,可实现高通量的肿瘤细胞球体生成和药物筛选,在化疗药物研发中具有广阔的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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