雌二醇对早幼粒细胞白血病衍生细胞株NB4中mir -21和miR-155表达的影响

IF 0.4 Q4 PEDIATRICS
Robab Naghibzadeh, N. Obeidi, Alireza Farsinejd, Gholamreza Khamisipour, Masoud Tohid Far
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引用次数: 0

摘要

由于雌激素参与调节干细胞的增殖和承诺,以及miR-21和miR-155表达对急性髓性白血病(AML)增殖和集落形成的影响,本研究的目的是评估雌二醇对急性早幼粒细胞白血病(APL) NB4细胞系中miR-21和miR-155表达的影响。材料与方法本实验采用不同剂量雌二醇(5、25、50、75、100、150、200、250 μg/ml)和对照处理NB4细胞24、48 h。分别用台盼蓝排除法、流式细胞术和MTT法测定细胞活力、细胞凋亡和细胞增殖。采用绝对定量实时PCR检测miR-155和miR-21的表达水平。结果雌二醇有效剂量(200 μg/ml)可降低NB4细胞活力(呈剂量依赖性,P = 0.004)并导致细胞凋亡。此外,miR-155、miR-21的表达显著且呈剂量依赖性降低(p<0.05)。结论雌二醇有效剂量可引起NB4细胞凋亡。这种物质可以作为治疗APL的药物。然而,需要进一步的评估来支持雌二醇治疗APL的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Estradiol on miR-21& miR-155 Expression in promyelocytic leukemia-derived cell line NB4
BackgroundDue to the estrogen participation in modulating the proliferation and commitment of stem cells and the effects of miR-21 and miR-155 expression on reduced proliferation and colony formation of acute myeloid leukemia (AML), the aim of the present study was to evaluate the effect of estradiol on expression of miR-21 and miR-155 in the NB4 cell line, as an acute promyelocytic leukemia (APL).Materials and MethodsIn the present experiment, NB4 cells were treated with different quantities of estradiol (5, 25, 50, 75, 100, 150, 200, 250 μg/ml) and vehicle control for 24 and 48 hours. Viability, apoptosis, and cellular proliferation were estimated by trypan blue exclusion, flow cytometry, and MTT assays, respectively. The level of miR-155 and miR-21 expression was studied using absolute quantitative real-time PCR.ResultsResults showed that estradiol in the effective dose (200 μg/ml) led to decreased cellular viability (in a dose dependent manner, P = 0.004) and apoptosis of NB4 cells. In addition, the expressions of miR-155 and miR-21 were significantly and dose-dependently decreased (p<0.05).ConclusionEstradiol at the effective dose caused apoptosis in NB4 cell line. This substance can be used as a drug for the treatment of APL. However, further assessments are needed to support the effectiveness of estradiol in the treatment of APL.
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来源期刊
CiteScore
0.80
自引率
33.30%
发文量
33
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