Imatinib: Difference between revisions
General information about an inhibitory drug used to treat specific cancers such as CML. |
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<br>'''<u>Clinical Pharmacology </u>'''<br>The [[Active site|active sites of]] tyrosine kinases each have a binding site for [[ATP|ATP.]] The catalysed enzymatic activity, known as protein tyrosine [[Phosphorylation|phosphorylation]] is the transfer of a terminal phosphate from ATP to tyrosine residues on its substrates. Deregulation of tyrosine kinase activity has been shown to play a central role in the pathogenesis of human cancers. | <br>'''<u>Clinical Pharmacology </u>'''<br>The [[Active site|active sites of]] tyrosine kinases each have a binding site for [[ATP|ATP.]] The catalysed enzymatic activity, known as protein tyrosine [[Phosphorylation|phosphorylation]] is the transfer of a terminal phosphate from ATP to tyrosine residues on its substrates. Deregulation of tyrosine kinase activity has been shown to play a central role in the pathogenesis of human cancers. | ||
<br>Imatinib works by binding close to the ATP binding site, locking it in a closed conformation, therefore inhibiting the enzyme activity of the protein semicompetitively. This process ultimately prevents the occurance of downstream signaling pathways which promote leukemogenesis.<ref name="(2)">Iqbal, N., &amp; Iqbal, N. (2014). Imatinib: a breakthrough of targeted therapy in cancer. Chemotherapy research and practice, 2014.[Available at]: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055302/</ref><br> | <br>Imatinib works by binding close to the ATP binding site, locking it in a closed conformation, therefore inhibiting the enzyme activity of the protein semicompetitively. This process ultimately prevents the occurance of downstream signaling pathways which promote leukemogenesis.<ref name="(2)">Iqbal, N., &amp;amp; Iqbal, N. (2014). Imatinib: a breakthrough of targeted therapy in cancer. Chemotherapy research and practice, 2014.[Available at]: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055302/</ref><br>''<br>'''''<u>Clinical implications :</u> ''''''<br>'''This medication is used to treat certain types of cancer such as chronic myeloid leukemia (CML) by Inhibiting at BCR-ABL gene on chromosome 22 (Philadelphia chromosome)<ref>Kang, Z. J., Liu, Y. F., Xu, L. Z., Long, Z. J., Huang, D., Yang, Y., Liu, B., Feng, J. X., Pan, Y. J., Yan, J. S., … Liu, Q. (2016). The Philadelphia chromosome in leukemogenesis. Chinese journal of cancer, 35, 48. doi:10.1186/s40880-016-0108-0. [Available at]:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896164/</ref>. It is a chemotherapy drug that works by slowing or stopping the growth of cancer cells.<br> | ||
= <br>'''References :''' = | = <br>'''References :''' = | ||
<references />'''<br><br>''' | <references />'''<br><br>''' | ||
Revision as of 17:15, 5 December 2018
Introduction
Imatinib (“Gleevec” or “Glivec”), is a 2-phenyl amino pyrimidine derivative. It can be classified as tyrosine kinase inhibitor (TKI) [1] .This protein has revolutionized the treatment of chronic myeloid leukemia (CML) in 2001.
Clinical Pharmacology
The active sites of tyrosine kinases each have a binding site for ATP. The catalysed enzymatic activity, known as protein tyrosine phosphorylation is the transfer of a terminal phosphate from ATP to tyrosine residues on its substrates. Deregulation of tyrosine kinase activity has been shown to play a central role in the pathogenesis of human cancers.
Imatinib works by binding close to the ATP binding site, locking it in a closed conformation, therefore inhibiting the enzyme activity of the protein semicompetitively. This process ultimately prevents the occurance of downstream signaling pathways which promote leukemogenesis.[2]
Clinical implications : '
'This medication is used to treat certain types of cancer such as chronic myeloid leukemia (CML) by Inhibiting at BCR-ABL gene on chromosome 22 (Philadelphia chromosome)[3]. It is a chemotherapy drug that works by slowing or stopping the growth of cancer cells.
References :
- ↑ Cancer Research UK, Imatinib(Glivec) [Available at]:https://www.cancerresearchuk.org/about-cancer/cancer-in-general/treatment/cancer-drugs/drugs/imatinib
- ↑ Iqbal, N., &amp; Iqbal, N. (2014). Imatinib: a breakthrough of targeted therapy in cancer. Chemotherapy research and practice, 2014.[Available at]: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055302/
- ↑ Kang, Z. J., Liu, Y. F., Xu, L. Z., Long, Z. J., Huang, D., Yang, Y., Liu, B., Feng, J. X., Pan, Y. J., Yan, J. S., … Liu, Q. (2016). The Philadelphia chromosome in leukemogenesis. Chinese journal of cancer, 35, 48. doi:10.1186/s40880-016-0108-0. [Available at]:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896164/