the association between prevalence of jak2v617f mutation and blood indicies in groups of patients with myeloproliferative neoplasms in rasul akram hospital

نویسندگان

akram asghari hematology-oncology department, rasul akram hospital, tehran university of medical sciences, tehran,

ali shahriari ahmadi hematology-oncology department, rasul akram hospital, tehran university of medical sciences, tehran, iran

ali basi hematology-oncology department, firoozgar hospital, tehran university of medical sciences, tehran, iran

masood vkili hematology-oncology department, rasul akram hospital, tehran university of medical sciences, tehran, iran

چکیده

introduction : myeloproliferative neoplasms (mpns) are a group of clonal malignant hematologic disease, where the main and common members are; polycythemia vera (pv), primary myelofibrosis (pmf), and essential thrombocytosis (et). these group of diseases are able to be transformed into each other. methods:   this cross sectional study conducted the evaluation of jak2v161f mutation in dna in peripheral blood of 91 patients with known or suspected diagnosis of mpns by real time pcr method and survey of peripheral blood smear. result: . prevalence of jak2v617f mutation between patients was %58.2 and pv had most common prevalence ratio between other groups. while mean age of patients was 50/9 yr (for 39.6% male and 60.4% female), three patients (equal of %3.3) were atypical presentation and 2 patients die due to malignant transformation. there were significant differences in age, wbc and plt (in pv) with prevalence of jak2v617f mutation. these differences were not significant in other group. discussion: current study showed a high rate of association between jak2v617f mutation in patients with pv, et, pmf in iranian patients. therefore, peripheral blood mutation screening for jak2 v617f can be incorporated into the initial evaluation of patients suspected to have chronic myeloproliferative neoplasm and used of this test for determining of association between jak2v617f mutation, treatment of patients with blood indexes and patients of prognosis.

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Myeloproliferative Neoplasms Associated with Mutation in JAK2V617F and Tyrosine Kinase Inhibitors as Therapeutic Strategy

MPNs including a heterogeneous group of clonal or oligoclonal hamtopathies characterized by proliferation and accumulation of mature myeloid cells. JAK2 tyrosine kinase mutation is the most common molecular lesion identified in 90% of cases. JAK2 is involved in EPO signaling pathway, and mutations in it lead to EPO-independent spontaneous phosphorylation. Most tyrosine kinase inhibitors (TKI) a...

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The Association Between JAK2V617F Mutation and Bone Marrow Fibrosis at Diagnosis in Patients with Philadelphia-Negative Chronic Myeloproliferative Neoplasms

OBJECTIVE Bone marrow fibrosis is the second most common complication that causes morbidity and mortality inpatients with Philadelphia-negative myeloproliferative neoplasms (MPNs). The aim of this study was to investigate theassociation between JAK2V617F mutation and bone marrow fibrosis at diagnosis in patients with MPNs. MATERIAL AND METHODS In total, 149 patients with MPNs were retrospecti...

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Evaluation of JAK2V617F mutation prevalence in myeloproliferative neoplasm by AS-RT-PCR

Abstract Objective JAK2 is a non-receptor tyrosine kinase that plays a major role in myeloid disorders. JAK2V617F mutation is characterized by a G to T transverse at nucleotide 1849 in exon 12 of the JAK2 gene, located on the chromosome 9p, leading to a substitution of valine to phenylalanine at amino acid position 617 in the JAK2 protein. Methods In this study we evaluated RNA from 89 pati...

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عنوان ژورنال:
international journal of hematology-oncology and stem cell research

جلد ۵، شماره ۴، صفحات ۱۰-۱۳

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