Radio-lncRNAs: Biological Function and Potential Use as Biomarkers for Personalized Oncology.
Joanna Kozłowska-MasłońKacper GuglasAnna PaszkowskaTomasz KolendaMarta PodralskaAnna TeresiakRenata BliźniakKatarzyna LamperskaPublished in: Journal of personalized medicine (2022)
Long non-coding RNAs (lncRNAs) consist of at least 200 nucleotides. Although these molecules do not code proteins, they carry many regulatory functions in normal cells, as well as in cancer cells. For instance, many of these molecules have been previously correlated with tumorigenesis of different cancers and their reaction to various stress factors, such as radiotherapy, chemotherapy, or reactive oxygen species (ROS). The lncRNAs are associated not only with dysregulation in cancers after applied treatment but also with beneficial effects that may be achieved by modulating their expression, often significantly enhancing the patients' outcomes. A multitude of these molecules was previously considered as potential biomarkers of tumor development, progression, or cells' response to radio- or chemotherapy. Irradiation, which is often used in treating numerous cancer types, is not always sufficient due to cells gaining resistance in multiple ways. In this review, studies considering lncRNAs and their reaction to radiotherapy were examined. These molecules were divided regarding their role in specific processes strictly related to irradiation, and their influence on this type of treatment was explained, showing how vast an impact they have on IR-supported combat with the disease. This review aims to shed some light on potential future lncRNA-based biomarkers and therapeutic targets.
Keyphrases
- induced apoptosis
- long non coding rna
- cell cycle arrest
- locally advanced
- reactive oxygen species
- poor prognosis
- early stage
- end stage renal disease
- signaling pathway
- cell death
- radiation induced
- radiation therapy
- network analysis
- ejection fraction
- newly diagnosed
- palliative care
- metabolic syndrome
- chronic kidney disease
- type diabetes
- adipose tissue
- papillary thyroid
- oxidative stress
- dna damage
- peritoneal dialysis
- cell proliferation
- combination therapy
- transcription factor
- young adults
- risk assessment
- weight loss
- genome wide analysis
- pi k akt
- binding protein
- lymph node metastasis
- genome wide identification