| Literature DB >> 25582384 |
Giovanna De Matteis1, Roberta Zanotti2, Sabrina Colarossi3, Caterina De Benedittis3, Andrès Garcia-Montero4, Massimiliano Bonifacio2, Marta Sartori5, Fiorenza Aprili5, Beatrice Caruso5, Elisa Paviati5, Giuseppe Carli2, Omar Perbellini2, Alberto Zamò6, Patrizia Bonadonna7, Giovanni Pizzolo8, Giancesare Guidi5, Giovanni Martinelli3, Simona Soverini3.
Abstract
Patients with Systemic Mastocytosis (SM) need a highly sensitive diagnostic test for D816V detection of the KIT receptor gene. Along with histology/cytology and flow cytometry evaluation, bone marrow (BM) from 110 consecutive adult patients referred with a suspicion of SM to Multidisciplinary Outpatient Clinic for Mastocytosis in Verona were tested both by Amplification Refractory Mutation System Reverse Transcriptase quantitative real time Polymerase Chain Reaction (ARMS-RT-qPCR) and RT-PCR+Restriction Fragment Length Polymorphism (RFLP) followed by Denaturing-High Performance Liquid Chromatography (D-HPLC) and Sanger sequencing. ARMS-RT-qPCR identified D816V mutation in 77 patients, corresponding to 100% of cases showing CD25(+) mast cells (MCs) whereas RT-PCR+RFLP/D-HPLC+sequencing revealed D816V mutations in 47 patients. According to the 2008 WHO criteria 75 SM, 1 Cutaneous Mastocytosis (CM), 1 monoclonal MC activation syndrome (MMAS), and 1 SM Associated with Haematologic Non-Mast Cell Disorder (SM-AHNMD) were diagnosed. Seventeen out 75 SM patients (23%) would have not satisfied sufficient WHO criteria on the basis of the sole RT-PCR+RFLP: these patients had significantly lower serum tryptase levels and amount of CD25(+) MCs. Therefore, ARMS-RT-qPCR might result particularly useful, in patients that do not fulfil major BM histological criterion, for the recognition of indolent SM with a very low MC burden.Entities:
Keywords: D-HPLC; D816V; KIT; Real time PCR; Sequencing; Systemic mastocytosis
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Year: 2014 PMID: 25582384 DOI: 10.1016/j.leukres.2014.11.029
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156