基质
体内
肿瘤进展
肿瘤微环境
弹性成像
癌症研究
病理
癌症
磁共振成像
生物物理学
生物
化学
医学
肿瘤细胞
免疫组织化学
内科学
超声波
放射科
生物技术
作者
Frank Sauer,Steffen Grosser,Mehrgan Shahryari,Alexander Hayn,Jing Guo,Jürgen Braun,Susanne Briest,Benjamin Wolf,Bahriye Aktas,Lars‐Christian Horn,Ingolf Sack,Josef A. Käs
标识
DOI:10.1002/advs.202303523
摘要
Abstract Cancer progression is caused by genetic changes and associated with various alterations in cell properties, which also affect a tumor's mechanical state. While an increased stiffness has been well known for long for solid tumors, it has limited prognostic power. It is hypothesized that cancer progression is accompanied by tissue fluidization , where portions of the tissue can change position across different length scales. Supported by tabletop magnetic resonance elastography (MRE) on stroma mimicking collagen gels and microscopic analysis of live cells inside patient derived tumor explants, an overview is provided of how cancer associated mechanisms, including cellular unjamming, proliferation, microenvironment composition, and remodeling can alter a tissue's fluidity and stiffness . In vivo, state‐of‐the‐art multifrequency MRE can distinguish tumors from their surrounding host tissue by their rheological fingerprints. Most importantly, a meta‐analysis on the currently available clinical studies is conducted and universal trends are identified. The results and conclusions are condensed into a gedankenexperiment about how a tumor can grow and eventually metastasize into its environment from a physics perspective to deduce corresponding mechanical properties. Based on stiffness, fluidity , spatial heterogeneity , and texture of the tumor front a roadmap for a prognosis of a tumor's aggressiveness and metastatic potential is presented.
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