کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2136354 1547906 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cell differentiation and the multiple drug resistance phenotype in human erythroleukemic cells
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی تحقیقات سرطان
پیش نمایش صفحه اول مقاله
Cell differentiation and the multiple drug resistance phenotype in human erythroleukemic cells
چکیده انگلیسی


• PMA not induces differentiation to megakaryocytes in Lucena cells.
• Alox-5 gene is suggested to be related to differentiation erythroleukemic cells.
• Firsthand Alox-5, Mdr1, Nanog, Oct-4 and Sox-2 genes expression in FEPS cells was seen.
• Oct-4 and Sox-2 gene expression is similar in MDR cell lines.
• Alox-5 gene is expressed reversed to Mdr1 gene in erythroleukemic cell lines.

The gene expression of Oct-4, a transcription factor and hematopoietic stem cell marker, is higher in Lucena lines, which is MDR, and the gene Alox-5 has also been implicated in the differentiation of some cell lines. The aim of this study was to compare the response to PMA-induced differentiation in MDR and non-MDR cells. We observed the differentiation to megakaryocytes in the K562 cell line, which is non-MDR. The expression of Alox-5 and Nanog genes was downregulated and that of Mdr-1 was upregulated in K562 cells. The Lucena cell line contained a higher number of megakaryocytes than the non-MDR, but this number was not altered by PMA, as well as Mdr-1 gene expression. However, Alox-5 expression was downregulated. Alox-5, Mdr-1, Nanog, Oct-4 and Sox-2 basal expression was also evaluated in the K562, Lucena and FEPS (also MDR) cell lines. The transcription factors gene expression was similar in MDR cell lines. The expression of Alox-5 was higher in the non-MDR cell line, while FEPS had the lowest expression of this gene. The opposite pattern was observed for Mdr-1 gene expression. These results suggest that the Alox-5 gene might play a role in the differentiation of these cell lines.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Leukemia Research - Volume 42, March 2016, Pages 13–20
نویسندگان
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