Publications by authors named "Jiequan Wang"

Synovial hyperplasia, inflammation and immune cell infiltration are the central pathological basis of rheumatoid arthritis (RA). Nonetheless, the cellular, molecular and immunological mechanisms of RA remain poorly understood. An integrated analysis of single-cell RNA (scRNA) and bulk RNA sequencing datasets‌ aimed to unravel the cellular landscape, differentiation trajectory, transcriptome signature, and immunoinfiltration feature of RA synovium.

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Rheumatoid arthritis (RA) is a common autoimmune disease whose pathogenesis is poorly understand. Gaps in laboratory biomarkers cause a lack of clinically available strategies for the early diagnosis and treatment of RA. This study aims to identify serum exosomal lncRNAs as promising biomarkers and to unravel potential mechanisms by which they affect characteristic genes of fibroblast-like synoviocytes (FLSs) to induce RA malignant properties.

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Article Synopsis
  • * Extracellular vesicles (EVs) play a critical role in facilitating communication between cells by transferring ncRNAs, which can influence the functions and activities of the recipient cells in RA.
  • * The review explores the levels of EVs and their ncRNA content in RA patients, discusses relevant signaling pathways, and highlights the therapeutic potential of using exosomes for gene therapy in RA treatment.
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Objective: The present study aims to investigate the effect of common cold on the serum clozapine concentrations in hospitalized patients with schizophrenia.

Methods: A total of 65 schizophrenic patients with common cold receiving clozapine treatment were retrospectively enrolled. The demographic data, medication situation, clozapine concentration, and parameters of routine haematological and biochemical laboratory tests were obtained from the medical record system.

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  • * This study investigated potential biomarkers by analyzing the expression of specific miRNAs in the plasma of AUD patients compared to healthy controls and used machine learning to identify those most relevant to AUD.
  • * The research identified 22 key miRNAs and established a network connecting these miRNAs to target genes in the hippocampus, offering insights that could improve the diagnosis and treatment of AUD moving forward.
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  • - Gout arthritis (GA) is an inflammatory condition caused by the buildup of monosodium urate crystals, influenced by genetic, environmental, and metabolic factors, leading to activation of the immune system due to persistent high uric acid levels.
  • - Current treatments for GA include anti-inflammatory drugs and uric acid-lowering agents, but their effectiveness is limited, and the underlying molecular mechanisms, especially regarding NLRP3 inflammasome activation, remain poorly understood.
  • - The NLRP3 inflammasome plays a crucial role in GA initiation and progression, making it a potential target for diagnosis and treatment; pharmacological inhibition of this inflammasome could lead to new therapeutic strategies, with ongoing research into natural products and novel
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  • Rheumatoid arthritis (RA) is an autoimmune disease characterized by chronic inflammation, with unclear mechanisms hindering early diagnosis and effective treatment.
  • This study analyzed multiple datasets to identify gene expressions in synovial tissues and blood to find potential diagnostic and therapeutic biomarkers for RA.
  • The research found 266 differentially expressed genes linked to immune signaling, with five specific genes showing high diagnostic potential and suggesting important roles in the disease's inflammatory processes.
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Alcohol use disorder (AUD) is one of the most prevalent neuropsychological disorders worldwide, and its pathogenesis is convoluted and poorly understood. There is considerable evidence demonstrating significant associations between multiple heritable factors and the onset and progression of AUD. In recent years, a substantial body of research conducted by emerging biotechnologies has increasingly highlighted the crucial roles of noncoding RNAs (ncRNAs) in the pathophysiology of mental diseases.

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Aims: The present study aimed to investigate how Schizophrenia (SCZ)-specific long non-coding RNAs (lncRNAs) served as competing endogenous RNAs (ceRNAs) to modulate the biological functions and pathways involved in the pathogenesis of SCZ.

Main Methods: Microarray dataset (GSE54913) was obtained from Gene Expression Omnibus (GEO) database. Differently expressed (DE) lncRNAs and mRNAs were identified by "limma" package.

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Histone acetyltransferases are responsible for histone acetylation, while histone deacetylases (HDACs) counteract histone acetylation. An unbalanced dynamic between histone acetylation and deacetylation may lead to aberrant chromatin landscape and chromosomal function. HDAC2, a member of class I HDAC family, serves a crucial role in the modulation of cell signaling, immune response and gene expression.

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Telomeres are "protective messengers" at the ends of eukaryotic chromosomes that protect them from degradation, end to end fusion and recombination. Admittedly, telomeres progressively shorten with age that can also be significantly accelerated by pathological conditions, which are often considered as potential contributors for cellular senescence. It is commonly believed that constant accumulation of senescent cells may lead to dysfunctional tissues and organs, thereby accelerating aging process and subsequent occurrence of age-related diseases.

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Telomeres, protective DNA-protein complexes at the end of eukaryotic linear chromosomes, play pivotal roles in the maintenance of genomic stability during cell division. When telomeres are severely shortened, cells stop dividing and die, consequently leading to tissues degeneration. Concretely, replicative senescence and genomic damage are generally accompanied with telomere shortening, which may be a potential contributor in the pathogenesis of neurological disorders.

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  • Innate immunity uses pattern recognition receptors (PRRs) such as NOD-like receptors (NLRs), which help detect invading pathogens and trigger inflammatory responses for their elimination.
  • NLRC5, a significant member of the NLR family, shows increased expression in immune cells during inflammation and is involved in various immune responses, though its role in immune diseases remains debated.
  • Despite NLRC5's potential as a therapeutic target due to its involvement in inflammation and immune diseases, the limited understanding of its functions and mechanisms complicates drug development, making further research essential.
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Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease and the pathogenesis remains unclear. Previous studies suggested that fibroblast-like synoviocytes (FLSs) play an important role in RA pathogenesis, including the injury of cartilage, the hyperplasia of the synovium and the release of inflammatory cytokines. We used complete Freund's adjuvant (CFA) induced rats as animal models for studying the RA pathogenesis.

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