Understanding the matrix: collagen modifications in tumors and their implications for immunotherapy.
Rowie BorstLinde MeyaardM Ines Pascoal RamosPublished in: Journal of translational medicine (2024)
Tumors are highly complex and heterogenous ecosystems where malignant cells interact with healthy cells and the surrounding extracellular matrix (ECM). Solid tumors contain large ECM deposits that can constitute up to 60% of the tumor mass. This supports the survival and growth of cancerous cells and plays a critical role in the response to immune therapy. There is untapped potential in targeting the ECM and cell-ECM interactions to improve existing immune therapy and explore novel therapeutic strategies. The most abundant proteins in the ECM are the collagen family. There are 28 different collagen subtypes that can undergo several post-translational modifications (PTMs), which alter both their structure and functionality. Here, we review current knowledge on tumor collagen composition and the consequences of collagen PTMs affecting receptor binding, cell migration and tumor stiffness. Furthermore, we discuss how these alterations impact tumor immune responses and how collagen could be targeted to treat cancer.
Keyphrases
- extracellular matrix
- induced apoptosis
- cell cycle arrest
- wound healing
- cell migration
- immune response
- tissue engineering
- healthcare
- endoplasmic reticulum stress
- cell death
- oxidative stress
- signaling pathway
- cell proliferation
- cell therapy
- climate change
- single cell
- drug delivery
- bone marrow
- dna binding
- inflammatory response