Neurofibromatosis in Children: Actually and Perspectives.
Maria Lucia SurIonel ArmatGenel SurDiana-Cristina PopGabriel SamașcaIulia LupanTeodora-Larisa TimisIoan Alexandru FlorianDaniel G SurPublished in: Children (Basel, Switzerland) (2022)
The three types of neurofibromatosis, namely type 1, type 2, and schwannomatosis, are generally associated with various benign tumors affecting the skin and the nervous system. On rare occasions, especially in patients with neurofibromatosis type 1 (NF1), malignant neoplasms may also be present, several of them possessing a more aggressive course than in individuals without this syndrome. As such, a clear delineation between the three variants of neurofibromatosis is crucial to establish the correct diagnosis and management, as well as predict the neoplasm-related outcomes. Neurofibromin, the principal product of the NF1 gene, is a potent inhibitor of cellular proliferation, having been linked to several key signaling pathways involved in tumor growth. Therefore, it may provide a useful therapeutic target for tumor management in these patients. In this article, we want to present the association between deficiency of neurofibromin and the consequences of the lack of this protein leading to different kinds of malignant tumors. The therapy is still uncertain and most therapeutic options are in development or clinical trials.
Keyphrases
- signaling pathway
- clinical trial
- pi k akt
- end stage renal disease
- copy number
- ejection fraction
- chronic kidney disease
- lps induced
- newly diagnosed
- oxidative stress
- young adults
- induced apoptosis
- epithelial mesenchymal transition
- type diabetes
- stem cells
- randomized controlled trial
- low grade
- adipose tissue
- immune response
- binding protein
- case report
- transcription factor
- mesenchymal stem cells
- soft tissue
- phase ii
- small molecule
- cell proliferation
- gene expression
- high grade
- bone marrow
- toll like receptor
- cell therapy