Activating mutations in the MAP-kinase pathway define non-ossifying fibroma of bone.
Daniel BaumhoerMichal KovacJan SperveslageBaptiste AmelineAnna-Christina StroblArthur KrauseMarcel TrautmannEva WardelmannMichaela NathrathSylvia HöllerJendrik HardesGeorg GoshegerAndreas H KriegVolker ViethRoberto TiraboscoFernanda AmaryAdrienne M FlanaganWolfgang HartmannPublished in: The Journal of pathology (2019)
Non-ossifying fibroma (NOF), which occasionally results in pathologic fracture, is considered the most common benign and self-limiting lesion of the growing skeleton. By DNA sequencing we have identified hotspot KRAS, FGFR1 and NF1 mutations in 48 of 59 patients (81.4%) with NOF, at allele frequencies ranging from 0.04 to 0.61. Our findings define NOF as a genetically driven neoplasm caused in most cases by activated MAP-kinase signalling. Interestingly, this driving force either diminishes over time or at least is not sufficient to prevent autonomous regression and resolution. Beyond its contribution to a better understanding of the molecular pathogenesis of NOF, this study adds another benign lesion to the spectrum of KRAS- and MAP-kinase signalling-driven tumours. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Keyphrases
- single molecule
- protein kinase
- signaling pathway
- tyrosine kinase
- high density
- wild type
- neoadjuvant chemotherapy
- circulating tumor
- lps induced
- bone mineral density
- randomized controlled trial
- single cell
- pi k akt
- inflammatory response
- low grade
- cell proliferation
- lymph node
- locally advanced
- radiation therapy
- immune response
- high grade
- postmenopausal women
- soft tissue
- hip fracture
- nuclear factor
- toll like receptor