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细胞增殖受体增强的 3D 高通量筛选模型,用于优化乳腺癌细胞的药物疗效评估。

Cell Proliferation Receptor-Enhanced 3D High-Throughput Screening Model for Optimized Drug Efficacy Evaluation in Breast Cancer Cells.

机构信息

Department of Biomedical Engineering, Gachon University, Seongnam 13120, Republic of Korea.

Central R & D Center, Medical & Bio Decision (MBD) Co., Ltd, Suwon 16229, Republic of Korea.

出版信息

Anal Chem. 2022 Aug 30;94(34):11838-11847. doi: 10.1021/acs.analchem.2c02222. Epub 2022 Aug 17.

Abstract

A higher correlation of epidermal growth factor receptor (EGFR)-targeting drugs has been reported with the use of the cell proliferation receptor-enhanced three-dimensional high-throughput screening model (CPRE 3D-HTS model) compared with two-dimensional (2D) cell-based HTS. A greater expression of differential human EGFR 2 (HER2) protein between HER2-positive and HER2-negative cell lines was observed in breast cancer (BC) cell lines cultured using the CPRE 3D-HTS model compared with 2D-cultured cells. When using 2D-cultured cells, properties such as the expression of the cell proliferation receptor are lost as the cells attach to the bottom of the well plate. In an effort to solve this problem, the CPRE 3D-HTS model expressing high cell proliferation receptors was optimized by the selection of alginate as the extracellular matrix. Results from the use of the CPRE 3D-HTS model showed higher drug resistance with increased expression of drug resistance-related proteins. Of particular interest, a higher correlation of HER2-targeted drugs was observed with the use of the CPRE 3D-HTS model. In order to validate this higher correlation of target drugs observed in the CPRE 3D-HTS model, the results of Western blot analysis and high content imaging analysis were analyzed, which confirmed that 3D-cultured BC cell lines showed a greater difference in the expression of HER2-positive and HER2-negative BC cell lines than 2D-cultured cells. Thus, the use of CPRE 3D-HTS using a 384-pillar plate resulted in increased accuracy when screening HER2-targeted drugs in BC, and it is a very useful platform for analyzing the efficacy of targeted drugs by enhancing the expression of HER2.

摘要

与二维(2D)细胞高通量筛选(HTS)相比,表皮生长因子受体(EGFR)靶向药物与细胞增殖受体增强的三维高通量筛选模型(CPRE 3D-HTS 模型)的相关性更高。在乳腺癌(BC)细胞系中使用 CPRE 3D-HTS 模型培养时,与 2D 培养的细胞相比,差异人 EGFR 2(HER2)蛋白在 HER2 阳性和 HER2 阴性细胞系之间的表达更高。当使用 2D 培养的细胞时,随着细胞附着在孔板底部,细胞增殖受体的表达等特性会丢失。为了解决这个问题,通过选择藻酸盐作为细胞外基质对表达高细胞增殖受体的 CPRE 3D-HTS 模型进行了优化。使用 CPRE 3D-HTS 模型的结果显示,随着耐药相关蛋白表达的增加,药物耐药性更高。特别值得注意的是,使用 CPRE 3D-HTS 模型观察到 HER2 靶向药物的相关性更高。为了验证 CPRE 3D-HTS 模型中观察到的靶药物更高的相关性,分析了 Western blot 分析和高内涵成像分析的结果,证实 3D 培养的 BC 细胞系在 HER2 阳性和 HER2 阴性 BC 细胞系之间的表达差异大于 2D 培养的细胞。因此,在 BC 中筛选 HER2 靶向药物时,使用 CPRE 3D-HTS 使用 384 柱板可提高准确性,并且通过增强 HER2 的表达,该平台是分析靶向药物疗效的非常有用的平台。

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