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表达 EGFR 家族受体的肿瘤的 3D 体外模型:研究受体生物学和靶向药物开发的有力工具。

3D in vitro models of tumors expressing EGFR family receptors: a potent tool for studying receptor biology and targeted drug development.

机构信息

Institute of Biology and Biomedicine, Lobachevsky University, 23 Gagarin ave., Nizhny Novgorod 603950, Russia; Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 16/10 Miklukho-Maklay St., Moscow 117997, Russia.

Institute of Biology and Biomedicine, Lobachevsky University, 23 Gagarin ave., Nizhny Novgorod 603950, Russia.

出版信息

Drug Discov Today. 2019 Jan;24(1):99-111. doi: 10.1016/j.drudis.2018.09.003. Epub 2018 Sep 8.

Abstract

Carcinomas overexpressing EGFR family receptors are of high clinical importance, because the receptors have prognostic value and are used as molecular targets for anticancer therapy. Insufficient drug efficacy necessitates further in-depth research of the receptor biology and improvement in preclinical stages of drug evaluation. Here, we review the currently used advanced 3D in vitro models of tumors, including tumor spheroids, models in natural and synthetic matrices, tumor organoids and microfluidic-based models, as a potent tool for studying EGFR biology and targeted drug development. We are especially focused on factors that affect the biology of tumor cells, causing modification in the expression and basic phosphorylation of the receptors, crosstalk with other signaling pathways and switch between downstream cascades, resulting ultimately in the resistance to antitumor agents.

摘要

过表达表皮生长因子受体家族的癌瘤具有重要的临床意义,因为这些受体具有预后价值,并被用作抗癌治疗的分子靶标。由于药物疗效不足,需要进一步深入研究受体生物学,并改进药物评价的临床前阶段。在这里,我们回顾了目前使用的肿瘤先进的 3D 体外模型,包括肿瘤球体、天然和合成基质模型、肿瘤类器官和基于微流控的模型,作为研究表皮生长因子受体生物学和靶向药物开发的有力工具。我们特别关注影响肿瘤细胞生物学的因素,这些因素导致受体的表达和基本磷酸化发生改变,与其他信号通路发生串扰,并在下游级联之间切换,最终导致对抗肿瘤药物产生耐药性。

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