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囊性包虫病患者的 microRNA 表达谱及可能的细胞途径鉴定。

MicroRNA expression profile in patients with cystic echinococcosis and identification of possible cellular pathways.

机构信息

Hacettepe University, Vocational School of Health Services, Adnan Saygun Street, D-Blocks, Altındag 06100, Ankara, Turkey.

Faculty of Pharmacy, Department of Biochemistry, Hacettepe University, Ankara, Turkey.

出版信息

J Helminthol. 2021 Jan 14;95:e1. doi: 10.1017/S0022149X2000098X.

Abstract

Cystic echinococcosis (CE) is a neglected tropical disease, caused by metacestode (larval) form of the Echinococcus granulosus sensu lato (sl) in humans. MicroRNAs (miRNAs) are small, stable, tissue-specific RNA molecules encoded by the genome that are not translated into proteins. Circulating miRNA expression profiles vary in health and disease. The aim of this study is to determine the altered cellular pathways in CE by comparing the miRNA profiles of controls and CE patients with active or inactive cysts. Following abdominal ultrasonography (US) examination, 20 patients diagnosed with active CE (CE1, CE2, CE3a and CE3b) or inactive CE (CE4 and CE5) and three healthy controls were included in the study. The expression profiles of 372 biologically relevant human miRNAs were investigated in serum samples from CE patients and healthy controls with miScript miRNA HC PCR Array. Compared with the control group, expression of 6 miRNAs (hsa-miR-4659a-5p, hsa-miR-4518, hsa-miR-3977, hsa-miR-4692, hsa-miR-181b-3p, hsa-miR-4491) and one miRNA (hsa-miR-4687-5p) were found to be downregulated in CE patients with active and inactive cysts, respectively (p < 0.05). For downregulated miRNAs in this study, predicted targets were found to be associated mainly with cell proliferation, apoptosis, cell-cell interactions and cell cycle regulation. Further studies in this direction may elucidate the pathogenesis of human CE and the relationship between CE and other pathologies.

摘要

囊性包虫病(CE)是一种被忽视的热带病,由细粒棘球绦虫(Echinococcus granulosus sensu lato,sl)的幼虫(蚴)期引起。微小 RNA(miRNA)是一类由基因组编码的、长度约为 22 个核苷酸的非编码小 RNA 分子,它们不翻译成蛋白质。在健康和疾病状态下,循环 miRNA 的表达谱存在差异。本研究旨在通过比较活动期和非活动期 CE 患者与健康对照的 miRNA 谱,确定 CE 中的改变细胞途径。在腹部超声(US)检查后,将 20 例经诊断为活动期 CE(CE1、CE2、CE3a 和 CE3b)或非活动期 CE(CE4 和 CE5)和 3 名健康对照纳入研究。使用 miScript miRNA HC PCR Array 检测血清样本中 372 种与生物学相关的人类 miRNA 的表达谱。与对照组相比,在活动期和非活动期 CE 患者中,有 6 种 miRNA(hsa-miR-4659a-5p、hsa-miR-4518、hsa-miR-3977、hsa-miR-4692、hsa-miR-181b-3p、hsa-miR-4491)和 1 种 miRNA(hsa-miR-4687-5p)的表达下调(p < 0.05)。在本研究中下调的 miRNA 的预测靶标主要与细胞增殖、凋亡、细胞-细胞相互作用和细胞周期调节有关。在这方面的进一步研究可能阐明人类 CE 的发病机制以及 CE 与其他病理的关系。

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