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Bcr-Abl tyrosine kinase inhibitors- current status

Bcr-Abl plays a central role in the development of chromosome positive leukaemia. Chronic Myeloid leukaemia occurs due to increase proliferation and resistance to apoptosis by Bcr-Abl positive cells. Imatinib (STI571) is the first drug in the family of Bcr-Abl tyrosine kinase inhibitors while Niloti...

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Autores principales: Mughal, Anum, Aslam, Hafiz Muhammad, Khan, Aga Muhammad Hammad, Saleem, Shafaq, Umah, Ribak, Saleem, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706229/
https://www.ncbi.nlm.nih.gov/pubmed/23787070
http://dx.doi.org/10.1186/1750-9378-8-23
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author Mughal, Anum
Aslam, Hafiz Muhammad
Khan, Aga Muhammad Hammad
Saleem, Shafaq
Umah, Ribak
Saleem, Maria
author_facet Mughal, Anum
Aslam, Hafiz Muhammad
Khan, Aga Muhammad Hammad
Saleem, Shafaq
Umah, Ribak
Saleem, Maria
author_sort Mughal, Anum
collection PubMed
description Bcr-Abl plays a central role in the development of chromosome positive leukaemia. Chronic Myeloid leukaemia occurs due to increase proliferation and resistance to apoptosis by Bcr-Abl positive cells. Imatinib (STI571) is the first drug in the family of Bcr-Abl tyrosine kinase inhibitors while Nilotinib (AMN107) and Dasatinib (BMS-345825) are second generation drugs that are intended to have less resistance and intolerance than imatinib. Ponatinib (AP24534) an orally active Bcr-Abl Tyrosine Kinase Inhibitor and Bafetinib (INNO-406) have efficacy against various point mutations in the Bcr-Abl kinase. 1, 3, 4 thiadiazole derivatives has also displayed moderate inhibitory action on both Abl and Src kinase family. However there are varieties of Bcr-Abl inhibitors but Nilotinib is still the frontline tyrosine kinase inhibitors.
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spelling pubmed-37062292013-07-10 Bcr-Abl tyrosine kinase inhibitors- current status Mughal, Anum Aslam, Hafiz Muhammad Khan, Aga Muhammad Hammad Saleem, Shafaq Umah, Ribak Saleem, Maria Infect Agent Cancer Letter to the Editor Bcr-Abl plays a central role in the development of chromosome positive leukaemia. Chronic Myeloid leukaemia occurs due to increase proliferation and resistance to apoptosis by Bcr-Abl positive cells. Imatinib (STI571) is the first drug in the family of Bcr-Abl tyrosine kinase inhibitors while Nilotinib (AMN107) and Dasatinib (BMS-345825) are second generation drugs that are intended to have less resistance and intolerance than imatinib. Ponatinib (AP24534) an orally active Bcr-Abl Tyrosine Kinase Inhibitor and Bafetinib (INNO-406) have efficacy against various point mutations in the Bcr-Abl kinase. 1, 3, 4 thiadiazole derivatives has also displayed moderate inhibitory action on both Abl and Src kinase family. However there are varieties of Bcr-Abl inhibitors but Nilotinib is still the frontline tyrosine kinase inhibitors. BioMed Central 2013-06-20 /pmc/articles/PMC3706229/ /pubmed/23787070 http://dx.doi.org/10.1186/1750-9378-8-23 Text en Copyright © 2013 Mughal et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Mughal, Anum
Aslam, Hafiz Muhammad
Khan, Aga Muhammad Hammad
Saleem, Shafaq
Umah, Ribak
Saleem, Maria
Bcr-Abl tyrosine kinase inhibitors- current status
title Bcr-Abl tyrosine kinase inhibitors- current status
title_full Bcr-Abl tyrosine kinase inhibitors- current status
title_fullStr Bcr-Abl tyrosine kinase inhibitors- current status
title_full_unstemmed Bcr-Abl tyrosine kinase inhibitors- current status
title_short Bcr-Abl tyrosine kinase inhibitors- current status
title_sort bcr-abl tyrosine kinase inhibitors- current status
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706229/
https://www.ncbi.nlm.nih.gov/pubmed/23787070
http://dx.doi.org/10.1186/1750-9378-8-23
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