Article
Different spectra of recurrent gene mutations in subsets of chronic lymphocytic leukemia harboring stereotyped B-cell receptors.
Haematologica - 1 Aug 2016
Sutton Lesley-Ann, Young Emma, Baliakas Panagiotis, Hadzidimitriou Anastasia, Moysiadis Theodoros, Plevova Karla, Rossi Davide, Kminkova Jana, Stalika Evangelia, Pedersen Lone Bredo, Malcikova Jitka, Agathangelidis Andreas, Davis Zadie, Mansouri Larry, Scarfò Lydia, Boudjoghra Myriam, Navarro Alba, Muggen Alice F, Yan Xiao-Jie, Nguyen-Khac Florence, Larrayoz Marta, Panagiotidis Panagiotis, Chiorazzi Nicholas, Niemann Carsten Utoft, Belessi Chrysoula, Campo Elias, Strefford Jonathan C, Langerak Anton W, Oscier David, Gaidano Gianluca, Pospisilova Sarka, Davi Frederic, Ghia Paolo, Stamatopoulos Kostas, Rosenquist Richard
Abstract excerpt
We report on markedly different frequencies of genetic lesions within subsets of chronic lymphocytic leukemia patients carrying mutated or unmutated stereotyped B-cell receptor immunoglobulins in the largest cohort (n=565) studied for this purpose. By combining data on recurrent gene mutations (BIRC3, MYD88, NOTCH1, SF3B1 and TP53) and cytogenetic aberrations, we reveal a subset-biased acquisition of gene...
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