Literature DB >> 27581134

Molecular Detection of BCR-ABL in Chronic Myeloid Leukemia.

Ya-Zhen Qin1, Xiao-Jun Huang2.   

Abstract

All chronic myeloid leukemia (CML) patients have the BCR-ABL fusion gene. The constitutively activated BCR-ABL tyrosine kinase is a critical pathogenetic event in CML. Tyrosine kinase inhibitors (TKIs), such as imatinib, are synthesized small molecules that primarily target BCR-ABL tyrosine kinases and have become a first-line treatment for CML. Detection of BCR-ABL transcript level by real-time quantitative polymerase chain reaction (RQ-PCR) is a clinical routine for evaluating TKI treatment efficacy and predicting long-term response. Furthermore, because they are a main TKI resistance mechanism, the BCR-ABL tyrosine kinase domain (TKD) point mutations that are detected by Sanger sequencing can help clinicians make decisions on subsequent treatment selections. Here, we present protocols for the two abovementioned molecular methods for CML analysis.

Entities:  

Keywords:  BCR-ABL; Chronic myeloid leukemia; Real-time quantitative polymerase chain reaction; Sanger sequencing; Tyrosine kinase inhibitor

Mesh:

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Year:  2016        PMID: 27581134     DOI: 10.1007/978-1-4939-4011-0_1

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Verbascoside potentiates the effect of tyrosine kinase inhibitors on the induction of apoptosis and oxidative stress via the Abl-mediated MAPK signalling pathway in chronic myeloid leukaemia.

Authors:  Gulsum Akgun-Cagliyan; Aysegul Cort-Donmez; Emine Kilic-Toprak; Fatih Altintas
Journal:  Exp Ther Med       Date:  2022-06-14       Impact factor: 2.751

2.  [Analysis of the efficacy and influencing factors of nilotinib or dasatinib as second- or third-line treatment in patients with chronic myeloid leukemia in the chronic phase and accelerated phase].

Authors:  T Yuan; Y Y Lai; Y Z Qin; H X Shi; X J Huang; Y Hou; Q Jiang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2020-02-14
  2 in total

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