Evidence map›Paper›PMID 40031981›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2025

[LINC00837/miR-671-5p/SERPINE2 functional axis promotes pathological processes of fibroblast-like synovial cells in rheumatoid arthritis].

Zhoufang Cao, Yuan Wang, Mengna Wang, Yue Sun, Feifei Liu

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Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zhoufang CaoFirst Clinical Medical College, Anhui University of Traditional Chinese Medicine, Hefei 230038, China.
Yuan WangFirst Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei 230031, China.
Mengna WangFirst Clinical Medical College, Anhui University of Traditional Chinese Medicine, Hefei 230038, China.
Yue SunFirst Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei 230031, China.
Feifei LiuFirst Clinical Medical College, Anhui University of Traditional Chinese Medicine, Hefei 230038, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the regulatory effect of LINC00837/miR-671-5p/SERPINE2 functional axis on pathological processes of fibroblast-like synovial cells (FLS) in rheumatoid arthritis (RA).

methodsRA-FLS were transfected with a LINC00837 overexpression plasmid (pcDNA3.1-LINC00837), a LINC00837 interference plasmid (siRNA-LINC00837), or their respective negative control plasmids (pcDNA3.1-NC and siRNA-NC). Dual luciferase was used to verify the targeting relationship between LINC00837 and miR-671-5p and between miR-671-5p and SERPINE2. RT-qPCR was used to detect the expression levels of LINC00837, miR-671-5p and SERPINE2 in normal FLS or the transfected cells, whose proliferation and migration abilities were assessed using Edu assay and scratch healing assay and by detecting the expression levels of Ki-67, PCNA, E-cadherin and N-cadherin with Western blotting. The changes in cellular secretion of the inflammatory cytokines (TNF‑α, IL-17, IL-4 and IL-10) were examined using ELISA.

resultsDual luciferase reporter gene assay showed that LINC00837 was capable of binding to the 3'-UTR of miR-671-5p, and the latter bound to the 3-UTR of SERPINE2 at specific binding sites between them. Compared with normal FLS, RA-FLS showed significantly increased expressions of LINC00837 and SERPINE2, lowered miR-671-5p expression and enhanced proliferation and migration abilities with increased expressions of pro-inflammatory cytokines and reduced expressions of anti-inflammatory cytokines. Transfection of RA-FLS with pcDNA-LINC00837 further enhanced cell proliferation and migration and the changes in the inflammatory cytokines, while transfection with si-LINC00837 produced the opposite changes.

conclusionsRA-FLS have a LINC00837/miR-671-5p/SERPINE2 functional axis, which regulates cell proliferation, migration and secretion of inflammatory factors, and interventions targeting LINC00837 may provide a potential strategy to regulate the pathological processes in RA-FLS.

Indexed as

Arthritis, RheumatoidFibroblastsMicroRNAsRNA, Long NoncodingSynoviocytesCell MovementCell ProliferationCells, CulturedHumansSynovial MembraneTransfectionMicroRNAsMIRN671 microRNA, humanRNA, Long Noncodingfibroblast-like synovial cellsinflammatory factorsLINC00837migrationproliferationrheumatoid arthritis

Identifiers

PMID40031981
PMCPMC11875867

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.