4.7 Review

Matrix proteoglycans in tumor inflammation and immunity

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 323, Issue 3, Pages C678-C693

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00023.2022

Keywords

dendritic; immunotherapy; matrix; proteoglycans; versican

Funding

  1. NationalInstitutes of Health (NIH)/National Cancer Institute [R01CA252937]
  2. American Cancer Society [127508-RSG-15-045-01-LIB]
  3. Leukemia and Lymphoma Society [6551-18]
  4. UW Trillium Myeloma Fund
  5. Robert J. Shillman Foundation

Ask authors/readers for more resources

Matrix proteoglycan signaling plays a crucial role in both the formation and inhibition of tumors, and this signaling is complex in cancer-restraining and cancer-promoting inflammation. The use of matrix diagnostics and therapeutics may help improve anti-cancer immunity.
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.

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