Non-coding RNAs in Brain Tumors, the Contribution of lncRNAs, circRNAs, and snoRNAs to Cancer Development-Their Diagnostic and Therapeutic Potential.
Julia LatowskaAdriana GrabowskaŻaneta ZarębskaKonrad KuczyńskiBogna KuczyńskaKatarzyna RollePublished in: International journal of molecular sciences (2020)
Brain tumors are one of the most frightening ailments that afflict human beings worldwide. They are among the most lethal of all adult and pediatric solid tumors. The unique cell-intrinsic and microenvironmental properties of neural tissues are some of the most critical obstacles that researchers face in the diagnosis and treatment of brain tumors. Intensifying the search for potential new molecular markers in order to develop new effective treatments for patients might resolve this issue. Recently, the world of non-coding RNAs (ncRNAs) has become a field of intensive research since the discovery of their essential impact on carcinogenesis. Some of the most promising diagnostic and therapeutic regulatory RNAs are long non-coding RNAs (lncRNAs), circular RNAs (circRNAs), and small nucleolar RNAs (snoRNAs). Many recent reports indicate the important role of these molecules in brain tumor development, as well as their implications in metastasis. In the following review, we summarize the current state of knowledge about regulatory RNAs, namely lncRNA, circRNAs, and snoRNAs, and their impact on the development of brain tumors in children and adults with particular emphasis on malignant primary brain tumors-gliomas and medulloblastomas (MB). We also provide an overview of how these different ncRNAs may act as biomarkers in these tumors and we present their potential clinical implications.
Keyphrases
- long non coding rna
- end stage renal disease
- healthcare
- transcription factor
- endothelial cells
- ejection fraction
- small molecule
- chronic kidney disease
- emergency department
- poor prognosis
- single cell
- young adults
- prognostic factors
- squamous cell carcinoma
- cell therapy
- high grade
- human health
- single molecule
- bone marrow
- drug induced
- patient reported