4.5 Article

Development of high-resolution melting analysis for the detection of the MYD88 L265P mutation

期刊

CLINICAL BIOCHEMISTRY
卷 46, 期 4-5, 页码 385-387

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.clinbiochem.2012.11.007

关键词

MYD88; Mutation; High-resolution melting analysis; Diffuse large B-cell lymphoma

资金

  1. Science and Technology Special Project in Clinical Medicine of Jiangsu Province [BL2012056]
  2. 333 Project of Jiangsu Province [BRA2011085]
  3. Natural Science Foundation of Jiangsu Province [BK2009206]
  4. Social Development Foundation of Zhenjiang [SH2010015, SH2011056]

向作者/读者索取更多资源

Objective: Recurrent L265P mutation of myeloid differentiation primary response gene 88 (MYD88) has been identified in a proportion of diffuse large B-cell lymphoma (DLBCL) and chronic lymphocytic leukemia. The present study aimed to establish a rapid, sensitive, and reliable method using high-resolution melting analysis (HRMA) to detect MYD88 L265P mutation in DLBCL. Designs and methods: The sensitivity of HRMA in the detection of MYD88 L265P mutation was evaluated. MYD88 L265P mutation was further screened in 120 patients with DLBCL The results of HRMA were validated by direct DNA sequencing. Results:. For the detection of MYD88 L265P mutation, the reproducible maximal sensitivity of HRMA was 5% higher than that obtained by direct DNA sequencing (25%). Heterozygous MYD88 L265P mutations were identified in 11(9.2%) DLBCL cases, all of which were diagnosed as non-germinal-center B cell (non-GCB) DLBCL. Conclusions: The HRMA assay is a rapid, sensitive, reliable, and high-throughput method to screen MYD88 L265P mutation and could be used in clinical diagnostic laboratories. 2012 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

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