Anexelekto (AXL) no more: microRNA-155 (miR-155) controls the "Uncontrolled" in SARS-CoV-2.
Konstantinos I PapadopoulosAlexandra PapadopoulouTar-Choon AwPublished in: Human cell (2024)
AXL is the gene that encodes the Anexelekto (AXL) receptor tyrosine kinase that demonstrates significant roles in various cellular processes, including cell growth, survival, and migration. Anexelekto is a Greek word meaning excessive and uncontrolled, semantically implying the crucial involvement of AXL in cancer and immune biology, and in promoting cancer metastasis. AXL overexpression appears to drive epithelial to mesenchymal transition, tumor angiogenesis, decreased antitumor immune response, and resistance to therapeutic agents. Recently, AXL has been reported to play important roles in several viral infections, including SARS-CoV-2. We have previously outlined the importance of microRNAs (miRNAs, miRs) and especially miR-155 in SARS-CoV-2 pathophysiology through regulation of the Renin-Angiotensin Aldosterone System (RAAS) and influence on several aspects of host innate immunity. MiRNAs are negative regulators of gene expression, decreasing the stability of target RNAs or limiting their translation and, enthrallingly, miR-155 is also involved in AXL homeostasis-both endogenously and pharmaceutically using repurposed drugs (e.g., metformin)-highlighting thrifty evolutionary host innate immunity mechanisms that successfully can thwart viral entry and replication. Cancer, infections, and immune system disturbances will increasingly involve miRNA diagnostics and therapeutics in the future.
Keyphrases
- tyrosine kinase
- sars cov
- epidermal growth factor receptor
- cell proliferation
- papillary thyroid
- gene expression
- long non coding rna
- immune response
- respiratory syndrome coronavirus
- squamous cell
- long noncoding rna
- dendritic cells
- lymph node metastasis
- genome wide
- small molecule
- transcription factor
- angiotensin ii
- squamous cell carcinoma
- endothelial cells
- weight gain
- vascular endothelial growth factor
- advanced cancer
- weight loss
- palliative care
- physical activity
- drug induced