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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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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. |
format | Online Article Text |
id | pubmed-3706229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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