LncRNA RNA143598的双重作用:类风湿关节炎的生物标志物及其在癌症中的意义

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Qiuhua Wu, Xiaoxia Zhang, Meiyun Qin, Danfei Shi, Yong Li
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引用次数: 0

摘要

目的:类风湿关节炎(RA)是一种具有复杂病理机制的慢性自身免疫性疾病,包括免疫系统失调和慢性炎症。最近的研究表明,长链非编码rna (LncRNAs)在免疫调节中发挥关键作用,并与多种疾病的发病机制有关,包括RA和各种类型的癌症。了解lncrna在RA中的参与及其在癌症中的潜在转录作用可以为疾病机制和治疗靶点提供新的见解。方法:使用GSE94519数据集,我们分析了RA患者和健康对照组的血清LncRNA谱。利用GEO2R技术鉴定了差异表达基因(DEGs),并通过定量聚合酶链反应(qPCR)对39例RA和53例健康样本进行了验证。采用受试者工作特征(ROC)分析评价诊断效果。使用TCGA数据对MTRNR2L1进行泛癌分析,并通过ssGSEA评估免疫浸润。结果:RNA143598在RA患者中表达显著上调,qPCR证实了其诊断潜力(AUC = 0.77)。泛癌分析显示,MTRNR2L1在胶质母细胞瘤(GBM)中高表达,在头颈部鳞状细胞癌(HNSC)中低表达,高表达与预后不良相关。免疫浸润分析显示MTRNR2L1与GBM中CD8 + T细胞、巨噬细胞和树突状细胞相关。结论:RNA143598是一种有前景的RA生物标志物,其转录基因MTRNR2L1在肿瘤预后和免疫调节中具有潜在的作用。这些发现为今后RA和癌症的靶向治疗研究奠定了基础。•RNA143598被确定为诊断类风湿关节炎(RA)的重要生物标志物,具有临床应用前景。•定量PCR验证了RNA143598的诊断潜力,曲线下面积(AUC)为0.77。•MTRNR2L1是RNA143598转录基因,在不同的癌症类型中表现出差异表达,在胶质母细胞瘤(GBM)中表达水平高与预后不良相关。•免疫浸润分析将MTRNR2L1表达与CD8 + T细胞、巨噬细胞和树突状细胞的存在联系起来,提示其在GBM中的免疫调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual roles of LncRNA RNA143598: a biomarker for rheumatoid arthritis and its implications in cancer.

Objective: Rheumatoid arthritis (RA) is a chronic autoimmune disease with complex pathological mechanisms, including immune system dysregulation and chronic inflammation. Recent studies indicate that long non-coding RNAs (LncRNAs) play key roles in immune regulation and have been implicated in the pathogenesis of multiple diseases, including RA and various types of cancer. Understanding the involvement of LncRNAs in RA and their potential transcriptional effects in cancer could provide novel insights into disease mechanisms and therapeutic targets.

Methods: Using the GSE94519 dataset, we analyzed serum LncRNA profiles from RA patients and healthy controls. Differential expression genes (DEGs) were identified using GEO2R, and findings were validated via quantitative polymerase chain reaction (qPCR) in 39 RA and 53 healthy samples. Receiver operating characteristic (ROC) analysis was performed to evaluate diagnostic performance. A pan-cancer analysis of MTRNR2L1 was conducted using TCGA data, with immune infiltration assessed via ssGSEA.

Results: RNA143598 was significantly upregulated in RA patients, and qPCR confirmed its diagnostic potential (AUC = 0.77). Pan cancer analysis shows that MTRNR2L1 is highly expressed in glioblastoma (GBM) and lowly expressed in head and neck squamous cell carcinoma (HNSC), with high GBM expression linked to poor prognosis. Immune infiltration analysis showed MTRNR2L1 correlated with CD8 + T cells, macrophages, and dendritic cells in GBM.

Conclusion: RNA143598 is a promising RA biomarker, and its transcription gene MTRNR2L1 demonstrates potential in cancer prognosis and immune regulation. These findings provide a foundation for future research on targeted therapies for RA and cancer. Key Points • RNA143598 is identified as a significant biomarker for diagnosing rheumatoid arthritis (RA), showing promise for clinical application. • Quantitative PCR validation demonstrates the diagnostic potential of RNA143598, with an area under the curve (AUC) of 0.77. • MTRNR2L1, which is RNA143598 transcribed gene, exhibits differential expression in different cancer types, with high levels associated with poor prognosis in glioblastoma (GBM). • Immune infiltration analysis links MTRNR2L1 expression to the presence of CD8 + T cells, macrophages, and dendritic cells, suggesting its role in immune regulation in GBM.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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