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原发性干燥综合征患者小唾液腺转录组和网络分析。

Transcriptomic and Network Analysis of Minor Salivary Glands of Patients With Primary Sjögren's Syndrome.

机构信息

Department of Oral Biology, State University of New York at Buffalo, Buffalo, NY, United States.

Genomics and Bioinformatics Core, State University of New York at Buffalo, Buffalo, NY, United States.

出版信息

Front Immunol. 2021 Jan 8;11:606268. doi: 10.3389/fimmu.2020.606268. eCollection 2020.

Abstract

Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease characterized primarily by immune-mediated destruction of exocrine tissues, such as those of the salivary and lacrimal glands, resulting in the loss of saliva and tear production, respectively. This disease predominantly affects middle-aged women, often in an insidious manner with the accumulation of subtle changes in glandular function occurring over many years. Patients commonly suffer from pSS symptoms for years before receiving a diagnosis. Currently, there is no effective cure for pSS and treatment options and targeted therapy approaches are limited due to a lack of our overall understanding of the disease etiology and its underlying pathology. To better elucidate the underlying molecular nature of this disease, we have performed RNA-sequencing to generate a comprehensive global gene expression profile of minor salivary glands from an ethnically diverse cohort of patients with pSS. Gene expression analysis has identified a number of pathways and networks that are relevant in pSS pathogenesis. Moreover, our detailed integrative analysis has revealed a primary Sjögren's syndrome molecular signature that may represent important players acting as potential drivers of this disease. Finally, we have established that the global transcriptomic changes in pSS are likely to be attributed not only to various immune cell types within the salivary gland but also epithelial cells which are likely playing a contributing role. Overall, our comprehensive studies provide a database-enriched framework and resource for the identification and examination of key pathways, mediators, and new biomarkers important in the pathogenesis of this disease with the long-term goals of facilitating earlier diagnosis of pSS and to mitigate or abrogate the progression of this debilitating disease.

摘要

原发性干燥综合征(pSS)是一种系统性自身免疫性疾病,主要表现为外分泌腺(如唾液腺和泪腺)的免疫介导破坏,分别导致唾液和泪液产生的丧失。这种疾病主要影响中年女性,通常以隐匿的方式发生,多年来腺体功能的细微变化逐渐积累。患者通常在被诊断为 pSS 之前多年就出现了 pSS 症状。目前,尚无有效的 pSS 治疗方法,由于我们对疾病的病因和潜在病理机制的总体理解有限,治疗选择和靶向治疗方法也受到限制。为了更好地阐明这种疾病的潜在分子性质,我们对来自不同种族 pSS 患者的小唾液腺进行了 RNA 测序,生成了一个全面的全局基因表达谱。基因表达分析确定了一些与 pSS 发病机制相关的途径和网络。此外,我们详细的综合分析揭示了原发性干燥综合征的分子特征,它可能代表着作为该疾病潜在驱动因素的重要参与者。最后,我们已经确定 pSS 中的全局转录组变化不仅可能归因于唾液腺中的各种免疫细胞类型,还可能归因于可能发挥作用的上皮细胞。总的来说,我们的综合研究为识别和研究该疾病发病机制中的关键途径、介质和新的生物标志物提供了一个丰富数据库的框架和资源,其长期目标是促进 pSS 的早期诊断,并减轻或消除这种使人衰弱的疾病的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d17/7821166/e6ee1d84da0f/fimmu-11-606268-g001.jpg

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