pdgfr α-介导的信号在胶质母细胞瘤耐药中的作用:体外研究。

IF 1.7 4区 生物学 Q4 CELL BIOLOGY
Sneha Raut, Meet Makwana, Prakash Pillai
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引用次数: 0

摘要

当细胞脱离细胞外基质(ECM)时,细胞会逃避程序性死亡,这是恶性胶质母细胞瘤(GBM)的一个关键特征,有助于肿瘤的存活、扩散和对治疗的抵抗。我们关注生长因子受体,特别是血小板衍生生长因子受体-α (PDGFRα)的作用,以及整合素表达模式在介导这种耐药性中的作用。我们首先在非贴壁条件下使用polyhema处理的板培养细胞以诱导对anoikis的抗性。我们进行了细胞存活、迁移和球体形成等实验。为了描述PDGFRα信号在anoikis耐药中的作用,我们进一步使用关键信号分子的药物抑制剂,如AG1295 (PDGFRα阻滞剂)、HS173 (PI3K抑制剂)、U0126 (ERK抑制剂)和AG490 (JAK-STAT抑制剂),导致细胞存活、增殖和迁移减少。这些发现强调了PDGFRα和相关信号通路在介导GBM的anoikis耐药中的关键作用,为干预提供了潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of PDGFRα-mediated signalling in anoikis resistance in glioblastoma: in vitro study.

Anoikis resistance, the evasion of programmed cell death when cells detach from the extracellular matrix (ECM), is a critical feature of glioblastoma (GBM) malignancy, contributing to tumor survival, spread, and resistance to therapy. We focused on the role of growth factor receptors, particularly platelet-derived growth factor receptor-α (PDGFRα), and integrin expression patterns in mediating this resistance. We first cultured cells under non-adherent conditions using polyHEMA-treated plates to induce anoikis resistance. We performed assays like cell survival, migration, and sphere formation. To delineate the role of PDGFRα signalling in anoikis resistance, we further employed pharmacological inhibitors of key signalling molecules such as AG1295 (PDGFRα blocker), HS173 (PI3K inhibitor), U0126 (ERK inhibitor), and AG490 (JAK-STAT inhibitor) which led to a decrease in cell survival, proliferation, and migration. These findings highlight the critical role of PDGFRα and associated signalling pathways in mediating anoikis resistance in GBM, offering potential therapeutic targets for intervention.

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来源期刊
CiteScore
3.70
自引率
4.80%
发文量
96
审稿时长
3 months
期刊介绍: In Vitro Cellular & Developmental Biology - Animal is a journal of the Society for In Vitro Biology (SIVB). Original manuscripts reporting results of research in cellular, molecular, and developmental biology that employ or are relevant to organs, tissue, tumors, and cells in vitro will be considered for publication. Topics covered include: Biotechnology; Cell and Tissue Models; Cell Growth/Differentiation/Apoptosis; Cellular Pathology/Virology; Cytokines/Growth Factors/Adhesion Factors; Establishment of Cell Lines; Signal Transduction; Stem Cells; Toxicology/Chemical Carcinogenesis; Product Applications.
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