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miR-574、miR-499、miR-125b、miR-106a和miR-9可能靶向参与炎症反应途径的TGFBR-1和TGFBR-2基因:慢性淋巴细胞白血病潜在的新型生物标志物。

miR-574, miR-499, miR-125b, miR-106a, and miR-9 potentially target TGFBR-1 and TGFBR-2 genes involving in inflammatory response pathway: Potential novel biomarkers for chronic lymphocytic leukemia.

作者信息

Hadi Nasrin, Namazi Faezeh, Ketabchi Fatemeh, Khosravian Farinaz, Nateghi Behnaz, Talebi Alireza, Baghi Masoud, Mianesaz Hamidreza, Zare Fateme, Salehi Mansoor

机构信息

Medical Genetics Research Center of Genome, Isfahan University of Medical Sciences, Isfahan, Iran; Cellular, Molecular and Genetics Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

Medical Biotechnology Research Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd, Iran.

出版信息

Pathol Res Pract. 2022 Oct;238:154077. doi: 10.1016/j.prp.2022.154077. Epub 2022 Aug 13.

Abstract

MicroARNAs (miRNAs) are linked to a variety of cancers, which resulted in molecular pathway dysregulation in chronic lymphocytic leukemia (CLL). Using five dysregulated miRNAs identified by literature mining and in silico analysis, we were able to demonstrate the critical role that the TGFBR1 and TGFB receptor signaling pathways play in the state of CLL. Assays using real-time PCR were run on 30 patients and 30 healthy controls. This study showed that patient samples have considerably higher levels of miR-574 and miR-499. Notably, the same groups had lower expression levels of miR-125b, miR-106a, and miR-9. Furthermore, we suggested that TGFBR1 and TGFBR2 expression levels were decreased in patients, and we suggested that these genes could be targets for our profile miRNAs. In the current study, we hypothesized that miR-574, miR-499, miR-125b, miR-106a, and miR-9 are likely five new potential biomarkers for early diagnosis. Our research also showed that these profile miRNAs have a role in the formation of CLL, possibly through controlling the TGFBR1 and TGFBR2 pathways. This suggests that these profile miRNAs could serve as biomarkers for the diagnosis and prognosis of CLL.

摘要

微小RNA(miRNA)与多种癌症相关,这导致慢性淋巴细胞白血病(CLL)中分子通路失调。通过文献挖掘和计算机分析鉴定出5种失调的miRNA,我们能够证明转化生长因子β受体1(TGFBR1)和转化生长因子β(TGFβ)受体信号通路在CLL状态中所起的关键作用。对30例患者和30名健康对照进行了实时聚合酶链反应检测。本研究表明,患者样本中miR-574和miR-499的水平显著更高。值得注意的是,同一组中miR-125b、miR-106a和miR-9的表达水平较低。此外,我们发现患者中TGFBR1和TGFBR2的表达水平降低,并且我们认为这些基因可能是我们所分析的miRNA的作用靶点。在当前研究中,我们假设miR-574、miR-499、miR-125b、miR-106a和miR-9可能是早期诊断的5种新的潜在生物标志物。我们的研究还表明,这些分析的miRNA可能通过控制TGFBR1和TGFBR2通路在CLL的形成中发挥作用。这表明这些分析的miRNA可作为CLL诊断和预后的生物标志物。

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