Regulation of Tumor Invasion by the Physical Microenvironment: Lessons from Breast and Brain Cancer

被引:22
作者
Beeghly, Garrett F. [1 ]
Amofa, Kwasi Y. [2 ,3 ]
Fischbach, Claudia [1 ,4 ]
Kumar, Sanjay [2 ,3 ,5 ,6 ]
机构
[1] Cornell Univ, Nancy E & Peter C Meinig Sch Biomed Engn, Ithaca, NY 14850 USA
[2] Univ Calif Berkeley Univ Calif San Francisco, Grad Program Bioengn, Berkeley, CA USA
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[4] Cornell Univ, Kavli Inst Cornell Nanoscale Sci, Ithaca, NY USA
[5] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[6] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
breast cancer; glioblastoma; physical microenvironment; mechanobiology; tumor invasion; engineering strategies; INTERSTITIAL FLUID PRESSURE; SMOOTH MUSCLE ACTIN; STEM-CELL NICHE; ON-A-CHIP; IN-VIVO; MECHANICAL-PROPERTIES; EPITHELIAL MORPHOGENESIS; VASCULAR NORMALIZATION; NUCLEAR-DEFORMATION; COLLECTIVE INVASION;
D O I
10.1146/annurev-bioeng-110220-115419
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The success of anticancer therapies is often limited by heterogeneity within and between tumors. While much attention has been devoted to understanding the intrinsic molecular diversity of tumor cells, the surrounding tissue microenvironment is also highly complex and coevolves with tumor cells to drive clinical outcomes. Here, we propose that diverse types of solid tumors share common physical motifs that change in time and space, serving as universal regulators of malignancy. We use breast cancer and glioblastoma as instructive examples and highlight how invasion in both diseases is driven by the appropriation of structural guidance cues, contact-dependent heterotypic interactions with stromal cells, and elevated interstitial fluid pressure and flow. We discuss how engineering strategies show increasing value for measuring and modeling these physical properties for mechanistic studies. Moreover, engineered systems offer great promise for developing and testing novel therapies that improve patient prognosis by normalizing the physical tumor microenvironment.
引用
收藏
页码:29 / 59
页数:31
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