Abstract

ABSTRACTObjective: This study aims to investigate the gene mutation characteristics of chronic neutrophilic leukaemia (CNL).Method: This study retrospectively analyses the molecular biological characteristics, laboratory characteristics and clinical data of four patients with CNL that were admitted in the second Hospital of Shanxi Medical University from May 2014 to October 2016. On the basis of the molecular biological data of 22 patients with CNL and 4 patients with CNL, we further analysed the characteristics of CNL molecular mutation.Results: Two out of the four patients with CNL were carriers of colony-stimulating factor 3 receptor (CSF3R) mutation, among which two were carriers of CSF3R T618I mutation combined with ASXL1 mutation and SETBP1 mutation, and two were only carriers of JAK2 V617F mutation. According to the molecular biological data of 22 patients with CNL, 20 patients were positive for CSF3R mutation. Two patients were positive for JAK2 V617F mutation. A total of 10 patients were positive for SETBP1 mutation which was correlated with the CSF3R T618I gene mutation (P = 0.03). A total of 13 patients were positive for ASXL1 mutation. No patients carried mutations in ASXL2 and MPL genes.Conclusion and Discussion: CSF3R mutation is the main tumorigenic mutation in CNL, in which CSF3R T618I mutation is the main mutation, and an extremely small number of CNL patients may be caused by JAK2 V617F mutation. SETBP1 and ASXL1 are the most common concomitant mutations in CNL with CSF3R mutation, and SETBP1 and CSF3R T618Imutations may have a certain correlation.

Highlights

  • Chronic neutrophilic leukaemia (CNL) is a potentially aggressive myeloprolife-rative neoplasm with a low incidence which is characterized mainly by a continuous increase in mature neutrophils in peripheral blood [1]

  • Two cases with Colony-stimulating factor 3 receptor (CSF3R) mutation were detected in four patients with CNL, all of which exhibited CSF3R T618I mutation combined with ASXL1(1c.2509C > T, 2c.2214C > A) and SETBP1mutations (D868N and I871 T)

  • In the present study, in addition to CSF3R mutation, JAK2 V617F, CALR, MPL, SETBP1, ASXL1 and ASXL2 gene mutations were analyzed in four patients with CNL

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Summary

Introduction

Chronic neutrophilic leukaemia (CNL) is a potentially aggressive myeloprolife-rative neoplasm with a low incidence which is characterized mainly by a continuous increase in mature neutrophils in peripheral blood [1]. Colony-stimulating factor 3 receptor (CSF3R) gene mutation is a highly specific and sensitive molecular marker of CNL [2,3]. Other mutated genes, such as JAK2 V617F and CALR, can be detected in some patientswith CNL [4,5,6,7,8], thereby suggesting that these mutated genes may be involved in CNL pathogenesis and development. The discovery of all mutated molecules suggested the heterogeneity of molecular pathogenesis in CNL. The molecular mutation characteristics of CNL are analysed based on the gene mutation in 4 patients with CNL in our hospital and in 18 patients in the literature to improve the understanding of the molecular mechanism of CNL

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