Human Vault RNAs: Exploring Their Potential Role in Cellular Metabolism.
Magdalena TaubeNatalia LisiakEwa TotońBłażej RubiśPublished in: International journal of molecular sciences (2024)
Non-coding RNAs have been described as crucial regulators of gene expression and guards of cellular homeostasis. Some recent papers focused on vault RNAs, one of the classes of non-coding RNA, and their role in cell proliferation, tumorigenesis, apoptosis, cancer response to therapy, and autophagy, which makes them potential therapy targets in oncology. In the human genome, four vault RNA paralogues can be distinguished. They are associated with vault complexes, considered the largest ribonucleoprotein complexes. The protein part of these complexes consists of a major vault protein (MVP) and two minor vault proteins (vPARP and TEP1). The name of the complex, as well as vault RNA, comes from the hollow barrel-shaped structure that resembles a vault. Their sequence and structure are highly evolutionarily conserved and show many similarities in comparison with different species, but vault RNAs have various roles. Vaults were discovered in 1986, and their functions remained unclear for many years. Although not much is known about their contribution to cell metabolism, it has become clear that vault RNAs are involved in various processes and pathways associated with cancer progression and modulating cell functioning in normal and pathological stages. In this review, we discuss known functions of human vault RNAs in the context of cellular metabolism, emphasizing processes related to cancer and cancer therapy efficacy.
Keyphrases
- endothelial cells
- gene expression
- papillary thyroid
- cell death
- cancer therapy
- endoplasmic reticulum stress
- oxidative stress
- transcription factor
- single cell
- squamous cell
- cell therapy
- stem cells
- palliative care
- signaling pathway
- induced pluripotent stem cells
- dna methylation
- mass spectrometry
- young adults
- pluripotent stem cells
- mesenchymal stem cells
- protein protein
- small molecule
- cell cycle arrest
- binding protein
- highly efficient
- childhood cancer
- chemotherapy induced
- molecularly imprinted