Abstract

Gliomas represent the most common malignant primary brain tumors, and a high-grade subset of these tumors including glioblastoma are particularly refractory to current standard-of-care therapies including maximal surgical resection and chemoradiation. The prognosis of patients with these tumors continues to be poor with existing treatments and understanding treatment failure is required. The dynamic interplay between the tumor and its microenvironment has been increasingly recognized as a key mechanism by which cellular adaptation, tumor heterogeneity, and treatment resistance develops. Beyond ongoing lines of investigation into the peritumoral cellular milieu and microenvironmental architecture, recent studies have identified the growing role of mechanical properties of the microenvironment. Elucidating the impact of these biophysical factors on disease heterogeneity is crucial for designing durable therapies and may offer novel approaches for intervention and disease monitoring. Specifically, pharmacologic targeting of mechanical signal transduction substrates such as specific ion channels that have been implicated in glioma progression or the development of agents that alter the mechanical properties of the microenvironment to halt disease progression have the potential to be promising treatment strategies based on early studies. Similarly, the development of technology to measure mechanical properties of the microenvironment in vitro and in vivo and simulate these properties in bioengineered models may facilitate the use of mechanical properties as diagnostic or prognostic biomarkers that can guide treatment. Here, we review current perspectives on the influence of mechanical properties in glioma with a focus on biophysical features of tumor-adjacent tissue, the role of fluid mechanics, and mechanisms of mechanical signal transduction. We highlight the implications of recent discoveries for novel diagnostics, therapeutic targets, and accurate preclinical modeling of glioma.

Highlights

  • Contemporary Management of Malignant Glioma and Biological ConsiderationsMortality due to cancer continues to rise worldwide with improving medical management of other disease processes

  • Malignant gliomas are a group of primary brain tumors that harbor a poor prognosis for afflicted patients [1, 2]

  • This group comprises the most common type of malignant glioma accounting for approximately 48.6% of all primary malignant brain tumors [1]

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Summary

INTRODUCTION

Mortality due to cancer continues to rise worldwide with improving medical management of other disease processes. Groups have been able to thoroughly characterize a few signal transduction pathways that utilize ligand-mediated, receptor-mediated, and integrin-mediated mechanosensation [45, 76, 77, 79, 95] Other studies in this area have focused on defining downstream components of signaling mediators following the initial mechanosensation event, and this has led to the identification YAP/TAZ, PHIP, and MGAT, among others that play a role in glioma stemness and disease progression; a unifying mechanism that considers heterogeneity in mechanical properties of the glioma microenvironment as well genetic and treatment-related drivers of plasticity is lacking and requires further investigation [96,97,98,99,100,101,102,103,104]. Further research is needed to establish and validate MRE as a reliable surrogate for such clinical

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