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	<updated>2026-04-14T23:53:08Z</updated>
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		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Imatinib&amp;diff=22827</id>
		<title>Imatinib</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Imatinib&amp;diff=22827"/>
		<updated>2018-12-05T17:15:06Z</updated>

		<summary type="html">&lt;p&gt;170762564: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;u&amp;gt;&#039;&#039;&#039;Introduction&#039;&#039;&#039;&amp;lt;/u&amp;gt;&amp;lt;br&amp;gt;Imatinib (“Gleevec” or “Glivec”), is a 2-phenyl amino pyrimidine derivative. It can be classified as tyrosine kinase [[Enzyme Inhibitors|inhibitor]] (TKI) &amp;lt;ref name=&amp;quot;(1)&amp;quot;&amp;gt;Cancer Research UK, Imatinib(Glivec) [Available at]:https://www.cancerresearchuk.org/about-cancer/cancer-in-general/treatment/cancer-drugs/drugs/imatinib&amp;lt;/ref&amp;gt; .This protein has revolutionized the treatment of [[Chronic myeloid leukimia|chronic myeloid leukemia ]](CML) in 2001. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;&#039;&#039;&#039;&amp;lt;u&amp;gt;Clinical Pharmacology&amp;amp;nbsp;&amp;lt;/u&amp;gt;&#039;&#039;&#039;&amp;lt;br&amp;gt;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.&amp;amp;nbsp;Deregulation of tyrosine kinase activity has been shown to play a central role in the pathogenesis of human cancers.&amp;amp;nbsp; &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;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.&amp;lt;ref name=&amp;quot;(2)&amp;quot;&amp;gt;Iqbal, N., &amp;amp;amp;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/&amp;lt;/ref&amp;gt;&amp;lt;br&amp;gt;&#039;&#039;&amp;lt;br&amp;gt;&#039;&#039;&#039;&#039;&#039;&amp;lt;u&amp;gt;Clinical implications&amp;amp;nbsp;:&amp;lt;/u&amp;gt;&amp;amp;nbsp;&#039;&#039;&#039;&#039;&#039;&#039;&amp;lt;br&amp;gt;&#039;&#039;&#039;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)&amp;lt;ref&amp;gt;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/&amp;lt;/ref&amp;gt;. It is a chemotherapy drug that works by slowing or stopping the growth of cancer cells.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
= &amp;lt;br&amp;gt;&#039;&#039;&#039;References&amp;amp;nbsp;:&#039;&#039;&#039;  =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&#039;&#039;&#039;&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>170762564</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Imatinib&amp;diff=22826</id>
		<title>Imatinib</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Imatinib&amp;diff=22826"/>
		<updated>2018-12-05T17:11:41Z</updated>

		<summary type="html">&lt;p&gt;170762564: General information about an inhibitory drug used to treat specific cancers such as CML.&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;u&amp;gt;&#039;&#039;&#039;Introduction&#039;&#039;&#039;&amp;lt;/u&amp;gt;&amp;lt;br&amp;gt;Imatinib (“Gleevec” or “Glivec”), is a 2-phenyl amino pyrimidine derivative. It can be classified as tyrosine kinase [[Enzyme Inhibitors|inhibitor]] (TKI) &amp;lt;ref name=&amp;quot;(1)&amp;quot;&amp;gt;Cancer Research UK, Imatinib(Glivec) [Available at]:https://www.cancerresearchuk.org/about-cancer/cancer-in-general/treatment/cancer-drugs/drugs/imatinib&amp;lt;/ref&amp;gt; .This protein has revolutionized the treatment of [[Chronic myeloid leukimia|chronic myeloid leukemia ]](CML) in 2001. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;&#039;&#039;&#039;&amp;lt;u&amp;gt;Clinical Pharmacology&amp;amp;nbsp;&amp;lt;/u&amp;gt;&#039;&#039;&#039;&amp;lt;br&amp;gt;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.&amp;amp;nbsp;Deregulation of tyrosine kinase activity has been shown to play a central role in the pathogenesis of human cancers.&amp;amp;nbsp; &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;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.&amp;lt;ref name=&amp;quot;(2)&amp;quot;&amp;gt;Iqbal, N., &amp;amp;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/&amp;lt;/ref&amp;gt;&amp;lt;br&amp;gt;&#039;&#039;&#039;&amp;lt;br&amp;gt;&amp;lt;u&amp;gt;Clinical implications&amp;amp;nbsp;:&amp;lt;/u&amp;gt;&amp;amp;nbsp;&#039;&#039;&#039;&#039;&#039;&#039;&amp;lt;br&amp;gt;&#039;&#039;&#039;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). It is a chemotherapy drug that works by slowing or stopping the growth of cancer cells.&amp;lt;br&amp;gt; &lt;br /&gt;
&lt;br /&gt;
= &amp;lt;br&amp;gt;&#039;&#039;&#039;References&amp;amp;nbsp;:&#039;&#039;&#039;  =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&#039;&#039;&#039;&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>170762564</name></author>
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