SLC25A38基因在急性淋巴细胞白血病患者中的差异表达

P. Prakash, S Kumar, Sanjay Kumar, hraddha Raj, Poonam Sinha
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引用次数: 0

摘要

SLC25A38基因产生的蛋白质属于线粒体溶质载体家族SLC25。它涉及凋亡途径,调节内在的caspase依赖性凋亡。目的:探讨急性淋巴细胞白血病(ALL)患者SLC25A38基因的表达水平。材料与方法:横断面研究于2019年4月至2020年3月在印度比哈尔邦巴特那英迪拉甘地医学科学研究所生物化学系进行。该研究包括30名白血病患者,其中25名成年男性,5名成年女性,10名健康志愿者作为对照组。采用实时定量聚合酶链反应检测ALL患者SLC25A38基因转化为甘油醛3-磷酸脱氢酶(GAPDH)基因相对于正常健康志愿者的表达水平。所有收集的数据均使用SPSS 16.0版社会科学统计软件包进行分析。结果:ALL患者SLC25A38基因转化为GAPDH的平均表达量是正常健康志愿者的5.3倍。2-∆∆Ct法测定表达倍数。胚细胞丰度与SLC25A38基因表达水平呈正相关(Pearson’s r=0.408, p=0.025)。其表达水平与骨髓中母细胞的比例有关。结论:SLC25A38基因高表达是ALL的共同特征,可能是一种新的预后和诊断生物标志物,也是ALL潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Expression of SLC25A38 Gene in Patients of Acute Lymphoblastic Leukaemia
Introduction: The SLC25A38 gene produces protein that belongs to the mitochondrial solute carrier family, SLC25. It is implicated in apoptotic pathways, which regulate intrinsic caspase-dependent apoptosis. Aim: To determine level of expression of SLC25A38 gene in patients of Acute Lymphoblastic Leukaemia (ALL). Materials and Methods: A cross-sectional study was done in the Department of Biochemistry, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India, from April 2019 to March 2020. The study included 30 leukaemia patients out of which 25 were adult males and five were adult females and 10 healthy volunteers were included as the control group. Level of expression of SLC25A38 gene normalised to Glyceraldehyde 3-phosphate Dehydrogenase (GAPDH) gene relative to normal healthy volunteers among the ALL patients was measured using quantitative real time polymerase chain reaction. All data collected were analysed using Statistical Package for the Social Sciences (SPSS) version 16.0 software. Results: An average of 5.3 fold expression of SLC25A38 gene normalised to GAPDH relative to normal healthy volunteer among the ALL patients was seen. The fold of expression was determined by 2-∆∆Ct method. There was a positive correlation between blast cell abundance and level of SLC25A38 gene expression (Pearson’s r=0.408, p=0.025). The expression level was found to be associated with the proportion of blast cells in the bone marrow. Conclusion: High expression of SLC25A38 gene is a common feature in ALL and may be a novel biomarker for prognosis and diagnosis, as well as a potential therapeutic target for ALL.
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