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Exploration of Dynamic Elastic Modulus Changes on Glioblastoma Cell Populations with Aberrant EGFR Expression as a Potential Therapeutic Intervention Using a Tunable Hyaluronic Acid Hydrogel Platform

机译:使用可调透明质酸水凝胶平台探讨EGFR异常表达作为胶质母细胞瘤细胞群体动态弹性模量的潜在治疗干预方法。

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摘要

Glioblastoma (GBM) is one of most aggressive forms of brain cancer, with a median survival time of 14.6 months following diagnosis. This low survival rate could in part be attributed to the lack of model systems of this type of cancer that faithfully recapitulate the tumor architecture and microenvironment seen in vivo in humans. Therapeutic studies would provide results that could be translated to the clinic efficiently. Here, we assess the role of the tumor microenvironment physical parameters on the tumor, and its potential use as a biomarker using a hyaluronic acid hydrogel system capable of elastic modulus tuning and dynamic elastic moduli changes. Experiments were conducted to assess the sensitivity of glioblastoma cell populations with different mutations to varying elastic moduli. Cells with aberrant epithelial growth factor receptor (EGFR) expression have a predilection for a stiffer environment, sensing these parameters through focal adhesion kinase (FAK). Importantly, the inhibition of FAK or EGFR generally resulted in reversed elastic modulus preference. Lastly, we explore the concept of therapeutically targeting the elastic modulus and dynamically reducing it via chemical or enzymatic degradation, both showing the capability to reduce or stunt proliferation rates of these GBM populations.
机译:胶质母细胞瘤(GBM)是脑癌的一种最具侵袭性的形式,诊断后中位生存时间为14.6个月。这种低的存活率可能部分归因于缺乏这种类型的癌症模型系统,无法忠实地概括人类体内所见的肿瘤结构和微环境。治疗研究将提供可有效转化为临床的结果。在这里,我们评估了肿瘤微环境物理参数在肿瘤上的作用,以及它的潜在用途,它是使用能够透明质酸调节和动态弹性模量变化的透明质酸水凝胶系统作为生物标志物的。进行实验以评估具有不同突变的胶质母细胞瘤细胞群体对变化的弹性模量的敏感性。具有异常上皮生长因子受体(EGFR)表达的细胞倾向于在较硬的环境中通过粘着斑激酶(FAK)感应这些参数。重要的是,抑制FAK或EGFR通常会导致反向的弹性模量偏爱。最后,我们探索了治疗上针对弹性模量并通过化学或酶促降解动态降低其弹性模量的概念,两者均显示出降低或阻碍这些GBM群体增殖速率的能力。

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