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									<identifier>oai:www.peertechzpublications.org:10.17352/2581-5407.000047</identifier>
									<datestamp>2022-10-11</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
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										The effects of thymoquinone and cytozine arabinoside on apoptosis and cell proliferation in acute myeloide leukemia
										</dc:title><dc:creator>Aslı Altun</dc:creator><dc:creator> Nurten Kara</dc:creator><dc:creator> Şengül Tural</dc:creator><dc:creator> Alişan Yıldıran</dc:creator><dc:creator>Leman Tomak</dc:creator><dc:description>&lt;p&gt;Purpose: The aim of this study was to investigate the effects of a chemotherapeutic agent Cytosine Arabinoside (Ara-C) and a natural anticancer agent of Thymoquinone (TQ) on apoptosis and cell proliferation of AML cell lines (Kasumi-6) both alone and in combined form.&lt;/p&gt;&lt;p&gt;Material and method: Kasumi-6 AML cells were treated with three different doses of Ara-C (0.1, 0.5 and 1 µmol) and TQ (25, 50 and 100 µM) for 48 and 72 hours incubations. After Annexin V and Propidium Iodide (PI) staining, apoptosis, viability, and cell proliferation were evaluated for each group in flow cytometry.&lt;/p&gt;&lt;p&gt;Results: As a result, AML cell lines showed a statistically significant difference in a single treatment of the active substances. Their combined treatment showed an increase in apoptosis and a decrease in viability in both groups at 48 and 72 hours incubation times (p &amp;lt; 0.001). In each group, it was observed that apoptosis was increased and viability was decreased and consequently cell proliferation was suppressed.&lt;/p&gt;&lt;p&gt;Conclusion: Ara-C was used for the first time in this study with TQ in AML. It was determined that the combined use of TQ and Ara-C did not have a synergistic effect on apoptosis.&lt;/p&gt;</dc:description>
										<dc:publisher>Global Journal of Cancer Therapy - Peertechz Publications</dc:publisher>
										<dc:date>2022-10-11</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/2581-5407.000047</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Aslı Altun et al.</dc:rights>
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