急性淋巴细胞白血病中的肿瘤干细胞

Azadeh Anbarlou, A. Atashi, M. A. Rahnama, M. Soleimani, S. Kaviani
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引用次数: 0

摘要

人们提出了不同的癌症发展模型。其中之一是癌症干细胞模型。在这个模型中,癌细胞的侵袭、复发和对抗癌药物的耐药都与这些细胞有关。最近,我们观察到t -急性淋巴母细胞白血病细胞系的一些群体表现出癌症干细胞的特性。这些细胞用CD133标记物检测。体外transwell实验显示CD133 + Jurkat细胞比CD133 - Jurkat细胞侵袭性更强,基因表达分析证实CD133 + Jurkat细胞高水平表达MMP9基因。CD133 +细胞经多柔比星处理后,Annexin-PI染色显示这些细胞对化疗药物具有高耐药性。我们证明化疗耐药可能是由于ABCG2基因的上调。此外,CD133 +细胞具有不受限制的增殖潜能,并能够分化为低生长潜能的细胞(CD133 -)。完全;我们证明CD133可以作为识别Jurkat细胞系中癌症干细胞的标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cancer stem cells in acute lymphoblastic leukemia
Different models were suggested for cancer development. One of them is cancer stem cell model. In this model, Invasion, relapse and resistance to anti-cancer drugs were seen in cancerous cells are related to these cells. Recently, weobserved that some of population in T-Acute lymphoblastic leukemia cell line display cancer stem cell properties. These cells were detected by CD133 marker. In vitro transwell assay showed that CD133 + Jurkat cells were more invasive than CD133 - Jurkat cells and also gene expression analysis confirmed CD133 + Jurkat cells expressed MMP9 gene in high levels. After treatment of CD133 + cells with doxorubicin, Annexin-PI staining showed that these cells have high resistance to chemotherapy drug. We demonstrated chemotherapy resistance may be because of up regulation of ABCG2 gene. In addition, CD133 + cells had unrestricted proliferation potential and were able to differentiate to cells with low growth potential (CD133 - ). Altogether; we demonstrated that CD133 could be as a marker to recognize cancer stem cells in Jurkat cell line.
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