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乳糜泻患者中选定基因和循环 microRNAs 的表达。

Expression of Selected Genes and Circulating microRNAs in Patients with Celiac Disease.

机构信息

4th Medical Clinic, Department 5-Internal Medicine, Faculty of Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400015 Cluj-Napoca, Romania.

Research Center for Functional Genomics, Biomedicine and Translational Medicine, Faculty of Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400337 Cluj-Napoca, Romania.

出版信息

Medicina (Kaunas). 2022 Jan 25;58(2):180. doi: 10.3390/medicina58020180.

DOI:10.3390/medicina58020180
PMID:35208504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8878253/
Abstract

: Celiac disease (CD) is an immune-mediated enteropathy with characteristic intestinal alterations. CD occurs as a chronic inflammation secondary to gluten sensitivity in genetically susceptible individuals. Until now, the exact cause of the disease has not been established, which is why new studies have appeared that address the involvement of various genes and microRNAs (miRNAs) in the pathogenesis. The aim of the study is to describe the expression of selected genes (Wnt family member 3, ; Wnt family member 11, ; tumor necrosis factor alpha, ; mitogen-activated protein kinase 1, ; AKT serine/threonine kinase 3, ; phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha, ; and cyclin ) and miRNAs (miR-192-5p, miR-194-5p, miR-449a and miR-638) in adult patients with CD. : In total, 15 patients with CD at diagnosis (newly diagnosed), 33 patients on a gluten-free diet (GFD) for at least 1 year and 10 controls (control) were prospectively included. Blood samples were evaluated by quantitative real-time polymerase chain reaction (qRT-PCR). : The results show that , and were significantly overexpressed ( = 0.0249, = 0.0019 and = 0.0275, respectively) when comparing the newly diagnosed group to the controls. The other genes studied in CD patients were mostly with high values compared to controls, without reaching statistical significance. Among the miRNAs, the closest to a statistically significant value was miR-194-5p when the newly diagnosed group versus control ( = 0.0510) and GFD group versus control ( = 0.0671) were compared. The DIANA and miRNet databases identified significant functional activity for miR-449a and miR-192-5p and an interconnection of miR-194-5p and miR-449a with . : In conclusion, genes and circulating miRNAs require further studies as they could represent important biomarkers in clinical practice.

摘要

: 乳糜泻(CD)是一种免疫介导的肠病,具有特征性的肠道改变。CD 是一种慢性炎症,发生于具有遗传易感性的个体对麸质敏感时。到目前为止,尚未确定该病的确切病因,因此出现了一些新的研究,探讨了各种基因和 microRNAs(miRNAs)在发病机制中的作用。本研究旨在描述选定基因(Wnt 家族成员 3,;Wnt 家族成员 11,;肿瘤坏死因子α,;丝裂原活化蛋白激酶 1,;AKT 丝氨酸/苏氨酸激酶 3,;磷脂酰肌醇-4,5-二磷酸 3-激酶催化亚单位α,;和细胞周期蛋白)和 miRNAs(miR-192-5p、miR-194-5p、miR-449a 和 miR-638)在成年 CD 患者中的表达。:共前瞻性纳入 15 例新诊断 CD 患者(新诊断组)、33 例接受无麸质饮食(GFD)至少 1 年的患者(GFD 组)和 10 名对照者(对照组)。采用实时定量聚合酶链反应(qRT-PCR)检测血样。:结果显示,与对照组相比,新诊断组中、和明显过表达(=0.0249、=0.0019 和=0.0275)。在 CD 患者中研究的其他基因与对照组相比,大多数基因值较高,但未达到统计学意义。在 miRNAs 中,新诊断组与对照组(=0.0510)和 GFD 组与对照组(=0.0671)相比,miR-194-5p 最接近统计学意义值。DIANA 和 miRNet 数据库鉴定出 miR-449a 和 miR-192-5p 的显著功能活性,并鉴定出 miR-194-5p 和 miR-449a 与的相互连接。:总之,基因和循环 miRNAs 需要进一步研究,因为它们可能是临床实践中的重要生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/b352d0d84718/medicina-58-00180-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/7ba154d37ae1/medicina-58-00180-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/1c6ed18acea1/medicina-58-00180-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/2b5a60704ad0/medicina-58-00180-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/cc8d7dca4ad9/medicina-58-00180-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/b352d0d84718/medicina-58-00180-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/7ba154d37ae1/medicina-58-00180-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/4f737cd83e50/medicina-58-00180-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/d0ad7cc11e01/medicina-58-00180-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/cd2fb6ee4d8f/medicina-58-00180-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/1c6ed18acea1/medicina-58-00180-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/2b5a60704ad0/medicina-58-00180-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/cc8d7dca4ad9/medicina-58-00180-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b44e/8878253/b352d0d84718/medicina-58-00180-g008.jpg

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