LINC00641/miR-378a and Their Cross-Talk with TNF-α/IFN-γ as Potential Biomarkers in Ulcerative Colitis and Crohn's Diseases.

IF 1.9 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nour A Abdel Hameed, Olfat G Shaker, Nabil A Hasona
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引用次数: 0

Abstract

The most well-known forms of inflammatory bowel disease (IBD) that affect the entire gastrointestinal tract are ulcerative colitis (UC) and Crohn's disease (CD). The serum profile of inflammatory biomarkers and noncoding RNA and their role in the propagation of the inflammatory process remains controversial. Thus, this study was designed to examine the relationship between hematological profile, C-reactive protein (CRP), tumor necrosis factor-alpha (TNF-α), interferon-gamma (INF-γ), and the expression of LINC00641 and miR-378a in individuals with IBDs. In addition, we elucidated the correlation between the expression of LINC00641 and miR-378a and the biochemical variables analyzed. This retrospective study analyzed 94 unrelated participants. Group I included healthy controls, Group II consisted of participants diagnosed with UC, and Group III consisted of participants diagnosed with CD. Patients with IBDs experienced significant elevations in CRP, total leukocyte count, platelets, erythrocyte sedimentation rate, TNF-α, and INF-γ. However, participants with IBD had lower hemoglobin and albumin levels than healthy control participants. Moreover, the expression levels of LINC00641 and miR-378a were elevated in participants with IBD, with a significant difference between participants with IBD and healthy controls. The most striking observation was a clear association between serum LINC00641 and miR-378a levels and the biochemical variables assessed. This study demonstrated a positive correlation between the expression of LINC00641/miR-378a and TNF-α in patients with UC and CD patients. This study suggests that LINC00641 and miR-378a are prospective biomarkers and noninvasive screening tools for IBDs, which may help predict the progression of complications.

LINC00641/miR-378a及其与TNF-α/IFN-γ的交互作用作为溃疡性结肠炎和克罗恩病的潜在生物标志物
最著名的影响整个胃肠道的炎症性肠病(IBD)形式是溃疡性结肠炎(UC)和克罗恩病(CD)。炎症生物标志物和非编码RNA的血清特征及其在炎症过程传播中的作用仍然存在争议。因此,本研究旨在检测ibd患者血液学特征、c反应蛋白(CRP)、肿瘤坏死因子α (TNF-α)、干扰素γ (INF-γ)与LINC00641和miR-378a表达之间的关系。此外,我们阐明了LINC00641和miR-378a的表达与所分析的生化变量之间的相关性。这项回顾性研究分析了94名不相关的参与者。I组包括健康对照组,II组包括诊断为UC的参与者,III组包括诊断为CD的参与者。ibd患者的CRP、白细胞总数、血小板、红细胞沉降率、TNF-α和INF-γ显著升高。然而,IBD患者的血红蛋白和白蛋白水平低于健康对照组。此外,在IBD参与者中,LINC00641和miR-378a的表达水平升高,IBD参与者与健康对照组之间存在显著差异。最引人注目的观察结果是血清LINC00641和miR-378a水平与评估的生化变量之间存在明确的关联。本研究证实了UC和CD患者中LINC00641/miR-378a与TNF-α的表达呈正相关。这项研究表明,LINC00641和miR-378a是ibd的前瞻性生物标志物和无创筛查工具,可能有助于预测并发症的进展。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
78
审稿时长
2.2 months
期刊介绍: Journal of Interferon & Cytokine Research (JICR) provides the latest groundbreaking research on all aspects of IFNs and cytokines. The Journal delivers current findings on emerging topics in this niche community, including the role of IFNs in the therapy of diseases such as multiple sclerosis, the understanding of the third class of IFNs, and the identification and function of IFN-inducible genes.
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