Hassani Saeed, Rostami Parsa, Pourtavakol Meshkat, Karamashtiani Amirhossein, Sayyadi Mohammad
Department of Medical Laboratory Sciences, School of Allied Medical Sciences, Arak University of Medical Sciences, Arak, Iran.
Department of Internal Medicine, School of Medical Sciences, Arak University of Medical Sciences, Arak, Iran.
Biochem Biophys Rep. 2024 Oct 18;40:101850. doi: 10.1016/j.bbrep.2024.101850. eCollection 2024 Dec.
Acute myeloid leukemia (AML) has been identified as a top priority for discovering a reliable biomarker for treatment improvement and patient outcome prediction due to the heterogeneous nature of AML and the obstacle to find an appropriate treatment strategy for this malignancy. Considering the involvement of long noncoding RNA (lncRNA) SNHG7 and BGL3 found in various cancers, the exact expression pattern of these lncRNAs and their clinical implications in acute myeloid leukemia (AML) continue to be elusive. In order to demonstrate a possible mechanism underlying AML pathogenesis, our goal was to examine BGL3 and SNHG7 lncRNA expressions in PI3K pathway.
This case-control cross-sectional study were conducted on RNA extracted from blood samples of 30 patients diagnosed with AML (Ayatollah-Khansari hospital, Arak, Iran) and 30 (age and gender matched) healthy controls. The expression levels of SNHG7 and BGL3 lncRNAs and their target genes Akt and PTEN, were measured using qRT-PCR. Subsequently, by means of statistical analysis, we determined the plausible correlation between the expressions of the aforementioned genes and lncRNA respectively.
In AML samples, a considerable increase in the expression levels of SNHG7 lncRNA and Akr gene was accompanied by a marked reduction in the expression levels of BGL3 lncRNA and PTEN gene. Nevertheless, No significant relationship between the expression level of the indicated genes/lncRNAs and age and sex was found. The remarkable correlation between the expression of genes/lncRNAs and the blast percentage in patients was the notable point in the result of this study.
As the most straightforward interpretation of our results, we propose that perhaps the association between SNHG7 and BGL3 built through the interaction between Akt and PTEN may play a crucial role in the AML pathogenesis and any element of this axis could be a potential novel target for further profound treatment strategies. Nonetheless, in the context of Hematological Malignancies, particularly AML, more detailed studies are needed in this area to elucidate the precise role played by this interesting testis-specific pathway.
由于急性髓系白血病(AML)具有异质性,且难以找到针对这种恶性肿瘤的合适治疗策略,因此确定一种可靠的生物标志物以改善治疗和预测患者预后已成为AML研究的首要任务。考虑到长链非编码RNA(lncRNA)SNHG7和BGL3在多种癌症中的作用,这些lncRNA在急性髓系白血病(AML)中的具体表达模式及其临床意义仍不明确。为了阐明AML发病机制的潜在机制,我们的目标是检测PI3K途径中BGL3和SNHG7 lncRNA的表达。
本病例对照横断面研究对从30例诊断为AML的患者(伊朗阿拉克阿亚图拉 - 汗萨里医院)和30例年龄及性别匹配的健康对照者的血液样本中提取的RNA进行检测。使用qRT-PCR测量SNHG7和BGL3 lncRNA及其靶基因Akt和PTEN的表达水平。随后,通过统计分析,我们分别确定了上述基因与lncRNA表达之间的可能相关性。
在AML样本中,SNHG7 lncRNA和Akr基因表达水平显著增加,同时BGL3 lncRNA和PTEN基因表达水平显著降低。然而,未发现所检测基因/lncRNA的表达水平与年龄和性别之间存在显著关系。本研究结果的显著之处在于基因/lncRNA表达与患者原始细胞百分比之间存在显著相关性。
作为对我们结果的最直接解释,我们提出,或许通过Akt与PTEN相互作用建立的SNHG7和BGL3之间的关联可能在AML发病机制中起关键作用,并且该轴的任何一个元素都可能成为进一步深入治疗策略的潜在新靶点。尽管如此,在血液系统恶性肿瘤,特别是AML的背景下,该领域需要更详细的研究来阐明这个有趣的睾丸特异性途径所起的精确作用。