Department of Pathology, University of California, San Francisco, USA.
Department of Biomedical Engineering, University of Minnesota, USA; University of Minnesota Physical Sciences in Oncology Center, USA; Masonic Cancer Center, University of Minnesota, USA; Institute for Engineering in Medicine, University of Minnesota, USA; Stem Cell Institute, University of Minnesota, USA.
Curr Opin Cell Biol. 2021 Oct;72:63-71. doi: 10.1016/j.ceb.2021.05.004. Epub 2021 Jun 27.
Organized extracellular matrix (ECM), in the form of aligned architectures, is a critical mediator of directed cancer cell migration by contact guidance, leading to metastasis in solid tumors. Current models suggest anisotropic force generation through the engagement of key adhesion and cytoskeletal complexes drives contact-guided migration. Likewise, disrupting the balance between cell-cell and cell-ECM forces, driven by ECM engagement for cells at the tumor-stromal interface, initiates and drives local invasion. Furthermore, processes such as traction forces exerted by cancer and stromal cells, spontaneous reorientation of matrix-producing fibroblasts, and direct binding of ECM modifying proteins lead to the emergence of collagen alignment in tumors. Thus, as we obtain a deeper understanding of the origins of ECM alignment and the mechanisms by which it is maintained to direct invasion, we are poised to use the new paradigm of stroma-targeted therapies to disrupt this vital axis of disease progression in solid tumors.
有序的细胞外基质 (ECM) 以定向排列的结构形式,通过接触导向作用是定向癌细胞迁移的关键介质,导致实体瘤转移。目前的模型表明,通过关键黏附和细胞骨架复合物的参与产生各向异性力,驱动接触导向迁移。同样,破坏肿瘤-基质界面处细胞与细胞-细胞外基质之间的力平衡,由 ECM 与细胞的相互作用驱动,会引发并驱动局部浸润。此外,诸如癌细胞和基质细胞施加的牵引力、产生基质的成纤维细胞自发的重新定向以及 ECM 修饰蛋白的直接结合等过程,导致肿瘤中胶原的定向排列。因此,随着我们对 ECM 排列的起源以及维持其定向侵袭的机制有了更深入的了解,我们有望利用针对基质的靶向治疗新范例来破坏实体瘤疾病进展这一重要轴。