The role of glycans in the mechanobiology of cancer.

J Biol Chem

Department of Biomedical Engineering, Texas A&M University, Houston, Texas, USA; Department of Biomedical Engineering, Texas A&M University, College Station, Texas, USA; Artie McFerrin Department of Chemical Engineering, Texas A&M University, College Station, Texas, USA; Department of Translational Medical Sciences, Texas A&M University, Houston, Texas, USA. Electronic address:

Published: March 2023

AI Article Synopsis

  • Cancer is influenced by both genetic factors and physical changes in the extracellular matrix, particularly its stiffening.
  • Cancer cells actively respond to these changes through a process called mechanotransduction, which promotes behavior like survival, proliferation, and migration.
  • Glycans, which are carbohydrate-based molecules, play a crucial role in this process by modifying the mechanical and biochemical environment during cancer progression, and there's ongoing research into how manipulating glycans could advance our understanding of cancer mechanobiology.

Article Abstract

Although cancer is a genetic disease, physical changes such as stiffening of the extracellular matrix also commonly occur in cancer. Cancer cells sense and respond to extracellular matrix stiffening through the process of mechanotransduction. Cancer cell mechanotransduction can enhance cancer-promoting cell behaviors such as survival signaling, proliferation, and migration. Glycans, carbohydrate-based polymers, have recently emerged as important mediators and/or modulators of cancer cell mechanotransduction. Stiffer tumors are characterized by increased glycan content on cancer cells and their associated extracellular matrix. Here we review the role of cancer-associated glycans in coupled mechanical and biochemical alterations during cancer progression. We discuss the recent evidence on how increased expression of different glycans, in the form of glycoproteins and proteoglycans, contributes to both mechanical changes in tumors and corresponding cancer cell responses. We conclude with a summary of emerging tools that can be used to modify glycans for future studies in cancer mechanobiology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930169PMC
http://dx.doi.org/10.1016/j.jbc.2023.102935DOI Listing

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