Division of Blood and Marrow Transplantation, Department of Medicine, University of California, San Diego (UCSD), La Jolla, California.
Moores Cancer Center, University of California, San Diego (UCSD), La Jolla, California.
Am J Physiol Cell Physiol. 2022 Sep 1;323(3):C678-C693. doi: 10.1152/ajpcell.00023.2022. Epub 2022 Jul 25.
Cancer immunoediting progresses through elimination, equilibrium, and escape. Each of these phases is characterized by breaching, remodeling, and rebuilding tissue planes and structural barriers that engage extracellular matrix (ECM) components, in particular matrix proteoglycans. Some of the signals emanating from matrix proteoglycan remodeling are readily co-opted by the growing tumor to sustain an environment of tumor-promoting and immune-suppressive inflammation. Yet other matrix-derived cues can be viewed as part of a homeostatic response by the host, aiming to eliminate the tumor and restore tissue integrity. These latter signals may be harnessed for therapeutic purposes to tip the polarity of the tumor immune milieu toward anticancer immunity. In this review, we attempt to showcase the importance and complexity of matrix proteoglycan signaling in both cancer-restraining and cancer-promoting inflammation. We propose that the era of matrix diagnostics and therapeutics for cancer is fast approaching the clinic.
癌症免疫编辑通过消除、平衡和逃逸三个阶段进行。每个阶段的特点是破坏、重塑和重建组织平面和结构屏障,这些屏障涉及细胞外基质(ECM)成分,特别是基质蛋白聚糖。基质蛋白聚糖重塑产生的一些信号很容易被生长中的肿瘤利用,以维持促进肿瘤和抑制免疫的炎症环境。然而,其他基质衍生的信号可以被视为宿主的一种动态平衡反应的一部分,旨在消除肿瘤并恢复组织完整性。这些后者的信号可以被用于治疗目的,以使肿瘤免疫微环境的极性向抗肿瘤免疫倾斜。在这篇综述中,我们试图展示基质蛋白聚糖信号在抑制和促进癌症炎症中的重要性和复杂性。我们提出,用于癌症的基质诊断和治疗的时代即将快速进入临床。