Decorin in the Tumor Microenvironment.

Adv Exp Med Biol

1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

Published: October 2020

AI Article Synopsis

  • The tumor microenvironment significantly impacts cancer development through interactions between tumor cells and the extracellular matrix.
  • Decorin is a key component in this process, recognized for its roles in inflammation and various cancers, acting as a natural inhibitor of growth factors and targeting multiple receptor tyrosine kinases (RTKs).
  • Decorin induces important anti-cancer effects, including cell cycle arrest, apoptosis, and processes that prevent metastasis and blood vessel formation, making it a promising therapeutic candidate for cancers reliant on RTK signaling.

Article Abstract

The tumor microenvironment plays a determining role in cancer development through a plethora of interactions between the extracellular matrix and tumor cells. Decorin is a prototype member of the SLRP family found in a variety of tissues and is expressed in the stroma of various forms of cancer. Decorin has gained recognition for its essential roles in inflammation, fibrotic disorders, and cancer, and due to its antitumor properties, it has been proposed to act as a "guardian from the matrix." Initially identified as a natural inhibitor of transforming growth factor-β, soluble decorin is emerging as a pan-RTK inhibitor targeting a multitude of RTKs, including EGFR, Met, IGF-IR, VEGFR2, and PDGFR. Besides initiating signaling, decorin/RTK interaction can induce caveosomal internalization and receptor degradation. Decorin also triggers cell cycle arrest and apoptosis and evokes antimetastatic and antiangiogenic processes. In addition, as a novel regulatory mechanism, decorin was shown to induce conserved catabolic processes, such as endothelial cell autophagy and tumor cell mitophagy. Therefore, decorin is a promising candidate for combatting cancer, especially the cancer types heavily dependent on RTK signaling.

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Source
http://dx.doi.org/10.1007/978-3-030-48457-6_2DOI Listing

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