Publications by authors named "Jiayao Hao"

Article Synopsis
  • Synovial hyperplasia and inflammation are key features of rheumatoid arthritis (RA), with fibroblast-like synoviocytes (FLSs) being major contributors to chronic inflammation and joint damage.
  • The study found that neutrophil extracellular traps (NETs) are significantly present in RA and activate ATP-citrate lyase (ACLY), which enhances the inflammatory response by affecting glucose metabolism and stimulating key signaling pathways.
  • Targeting ACLY could be a promising therapeutic strategy to reduce inflammation and joint injuries associated with RA, as indicated by its role in activating RA-FLSs and contributing to disease severity.
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Objective: Fibroblast-like synoviocytes (FLS) play a critical role on the exacerbation and deterioration of rheumatoid arthritis (RA). Aberrant activation of FLS pyroptosis signaling is responsible for the hyperplasia of synovium and destruction of cartilage of RA. This study investigated the screened traditional Chinese medicine berberine (BBR), an active alkaloid extracted from the Coptis chinensis plant, that regulates the pyroptosis of FLS and secretion of inflammatory factors in rheumatoid arthritis.

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Background: Mammalian STE20-like kinase 1 (MST1) is involved in the occurrence of cancer and autoimmune diseases by regulating cell proliferation, differentiation, apoptosis and other functions. However, its role and downstream targets in rheumatoid arthritis (RA) remain unclear.

Methods: The model of RA fibroblast-like synoviocytes (RA-FLSs) overexpressing MST1 was constructed by lentiviral transfection in vitro and analyzed the effects of MST1 on apoptosis, migration, invasion, and inflammation of RA-FLSs.

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Rheumatoid arthritis (RA) is an enduring, progressive autoimmune disorder. Abnormal activation of fibroblast-like synoviocytes (FLSs) has been proposed as the initiating factor for inflammation of the synovium and bone destruction. Neutrophil extracellular traps (NETs), which are web-like structures composed of DNA, histones, and granule proteins, are involved in the development of RA in multiple aspects.

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Background: The systemic immune-inflammation index (SII) is a cost-efficient indicator for carcinoma prognosis. However, its utility in urothelial carcinoma (UC) prognosis is disputed. This meta-analysis aims to assess SII's prognostic value in UC.

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