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BRAFV600E-mutation is invariably present and associated to oncogene-induced senescence in Erdheim-Chester disease.

Authors :
Cangi, Maria Giulia
Biavasco, Riccardo
Cavalli, Giulio
Grassini, Greta
Dal-Cin, Elena
Campochiaro, Corrado
Guglielmi, Barbara
Berti, Alvise
Lampasona, Vito
von Deimling, Andreas
Sabbadini, Maria Grazia
Ferrarini, Marina
Doglioni, Claudio
Dagna, Lorenzo
Source :
Annals of the Rheumatic Diseases; Aug2015, Vol. 74 Issue 8, p1596-1602, 7p, 2 Color Photographs, 2 Charts, 1 Graph
Publication Year :
2015

Abstract

Objectives Erdheim-Chester disease (ECD) is a rare form of histiocytosis characterised by uncontrolled chronic inflammation. The oncogenic BRAF <superscript>V600E</superscript> mutation has been reported in biopsies in 19 out of 37 patients with ECD from the largest published cohort, but never found in the patients' peripheral blood. Also, the role of the mutation in the pathogenesis of the disease has not been elucidated yet. BRAF <superscript>V600E</superscript> has been associated with oncogene-induced senescence (OIS), a protective mechanism against oncogenic events, characterised by the induction of proinflammatory pathways. Methods We verified the BRAF status in biopsies and peripheral blood from 18 patients with ECD from our cohort and matched controls by means of immunohistochemistry and of an ultrasensitive assay, based on the combination of a locked nucleic acid PCR and pyrosequencing. Droplet digital PCR was used to confirm the findings. We also evaluated the presence of senescence markers in ECD histiocytes. Results BRAF <superscript>V600E</superscript> mutation was present in all the biopsy and peripheral blood samples from patients with ECD and in none of the controls. ECD histiocytes and a fraction of circulating monocytes from patients with ECD showed signs of a constitutive activation of the MAPK pathway. Moreover, BRAF-mutated histiocytes expressed markers of OIS. Conclusions The oncogenic BRAF <superscript>V600E</superscript> mutation is present in biopsies and in the peripheral blood from all patients with ECD who were evaluated and is associated with OIS. These findings have significant implications for the pathogenesis, diagnosis and treatment of ECD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00034967
Volume :
74
Issue :
8
Database :
Complementary Index
Journal :
Annals of the Rheumatic Diseases
Publication Type :
Academic Journal
Accession number :
108385477
Full Text :
https://doi.org/10.1136/annrheumdis-2013-204924