Axl和血管内皮生长因子受体在单层和球状高分化浆液性卵巢癌模型中的膜定位和异质性变化

IF 2 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
GEN biotechnology Pub Date : 2023-02-01 Epub Date: 2023-02-15 DOI:10.1089/genbio.2022.0034
Yingye Fang, Princess I Imoukhuede
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引用次数: 0

摘要

血管内皮生长因子受体(VEGFR)和Axl是卵巢癌治疗中的靶向受体酪氨酸激酶(RTK)。二维单层培养和三维球形培养是 RTK 靶向药物筛选的常用模型:单层培养简单经济,而球形培养则包括多种遗传和组织学肿瘤特征。RTK的膜定位决定了RTK的信号转导和药物反应,但在这些模型中并没有表征。我们量化了质膜 RTK 的浓度,并显示了单层与球体内 RTK 丰度和异质性的差异。我们发现 OVCAR8 球形细胞质膜上的 VEGFR1 浓度比单层细胞高 10 倍;OVCAR8 球形细胞的异质性比单层细胞更高,表现出低 Axl(6200/细胞)和高 Axl 亚群(25000/细胞)的双峰分布。此外,质膜 Axl 浓度在化疗敏感细胞(OVCAR3)和化疗耐受细胞(OVCAR8)之间相差 100 倍,在化疗耐受细胞系(OVCAR5 与 OVCAR8)之间相差 10 倍。这些系统性的发现可以指导卵巢癌模型的药物筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Axl and Vascular Endothelial Growth Factor Receptors Exhibit Variations in Membrane Localization and Heterogeneity Across Monolayer and Spheroid High-Grade Serous Ovarian Cancer Models.

Vascular endothelial growth factor receptors (VEGFRs) and Axl are receptor tyrosine kinases (RTK) that are targeted in ovarian cancer therapy. Two-dimensional monolayer culture and three-dimensional spheroids are common models for RTK-targeted drug screening: monolayers are simple and economical while spheroids include several genetic and histological tumor features. RTK membrane localization dictates RTK signaling and drug response, however, it is not characterized in these models. We quantify plasma membrane RTK concentrations and show differential RTK abundance and heterogeneity in monolayers versus spheroids. We show VEGFR1 concentrations on the plasma membrane to be 10 times higher in OVCAR8 spheroids than in monolayers; OVCAR8 spheroids are more heterogeneous than monolayers, exhibiting a bimodal distribution of a low-Axl (6200/cell) and a high-Axl subpopulation (25,000/cell). In addition, plasma membrane Axl concentrations differ by 100 times between chemosensitive (OVCAR3) and chemoresistant (OVCAR8) cells and by 10 times between chemoresistant cell lines (OVCAR5 vs. OVCAR8). These systematic findings can guide ovarian cancer model selection for drug screening.

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