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March 3, 2026Arthritis Research & TherapyOpen Access

MSMP promotes an aberrant phenotype of fibroblast-like synoviocytes in rheumatoid arthritis by blocking autophagy via the RUNX1/GPR137B axis

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Authors

CWCuicui WangYZYanting ZengPTP Q Tan

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Overview

Observational analysis reveals MSMP promotes aberrant fibroblast-like synoviocyte behavior in rheumatoid arthritis, suggesting new therapeutic targets.

Key Points

  • MSMP levels are significantly elevated in fibroblast-like synoviocytes from rheumatoid arthritis patients, impacting joint deterioration.
  • Key findings indicate that MSMP knockdown significantly reduces RA fibroblast-like synoviocytes' migration and invasion capabilities.
  • Utilizing RNA expression analysis and protein assays, this study identifies RUNX1 as a transcription factor regulating GPR137B involved in MSMP signaling.
  • Intra-articular treatment with Ad-shRNA-MSMP showed potential to alleviate arthritis severity in a collagen-induced arthritis model.

Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/69a76629badf0bb9e87dbf40https://doi.org/10.1186/s13075-026-03755-4
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