Translational regulation of cell invasion through extracellular matrix-an emerging role for ribosomes.
David R SherwoodIsabel W Kenny-GanzertSiddharthan Balachandar ThendralPublished in: F1000Research (2023)
Many developmental and physiological processes require cells to invade and migrate through extracellular matrix barriers. This specialized cellular behavior is also misregulated in many diseases, such as immune disorders and cancer. Cell invasive activity is driven by pro-invasive transcriptional networks that activate the expression of genes encoding numerous different proteins that expand and regulate the cytoskeleton, endomembrane system, cell adhesion, signaling pathways, and metabolic networks. While detailed mechanistic studies have uncovered crucial insights into pro-invasive transcriptional networks and the distinct cell biological attributes of invasive cells, less is known about how invasive cells modulate mRNA translation to meet the robust, dynamic, and unique protein production needs of cell invasion. In this review we outline known modes of translation regulation promoting cell invasion and focus on recent studies revealing elegant mechanisms that expand ribosome biogenesis within invasive cells to meet the increased protein production requirements to invade and migrate through extracellular matrix barriers.
Keyphrases
- extracellular matrix
- induced apoptosis
- cell cycle arrest
- signaling pathway
- gene expression
- endoplasmic reticulum stress
- binding protein
- cell adhesion
- long non coding rna
- poor prognosis
- mesenchymal stem cells
- single cell
- cell proliferation
- epithelial mesenchymal transition
- small molecule
- amino acid
- anti inflammatory