Evidence map›Paper›PMID 32881056›Full record

ArticleJournal of clinical laboratory analysis2020

Long non-coding RNA XIST binding to let-7c-5p contributes to rheumatoid arthritis through its effects on proliferation and differentiation of osteoblasts via regulation of STAT3.

Zong-Qiang Wang, Dian-Hui Xiu, Jin-Lan Jiang, Gui-Feng Liu

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Journal of clinical laboratory analysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. The lncRNA XIST/miR-150-5p/c-Fos axis regulates sepsis-induced myocardial injury via TXNIP-modulated pyroptosis.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  10. Review
  11. Article
  12. Biological Function of Long Non-coding RNA (LncRNA) Xist.Frontiers in cell and developmental biology · 2021
    Review
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Zong-Qiang WangMedical Department, China-Japan Union Hospital of Jilin University, Changchun, China.
Dian-Hui XiuDepartment of Radiology, China-Japan Union Hospital of Jilin University, Changchun, China.
Jin-Lan JiangDepartment of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, China.
Gui-Feng LiuDepartment of Radiology, China-Japan Union Hospital of Jilin University, Changchun, China.ORCID https://orcid.org/0000-0001-6851-8293
Union Hospital · CN

Funding

National Youth Science Foundation of China 80151459The Education Department of Jilin Province 13th Five-Year Science and Technology Research Project 2016-No. 467
6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA), a chronic autoimmune disease, affects around 1% population worldwide, with the life quality of patients severely reduced. In this study, it is intended to explore the role of long non-coding RNA X-inactive specific transcript (lncRNA XIST) in RA and the underlying mechanisms associated with let-7c-5p and signal transducer and activator of transcription 3 (STAT3).

methodsLncRNA XIST, let-7c-5p, and STAT3 expressions were determined in RA and normal cartilage tissues, and their relationship was analyzed in osteoblasts. The regulatory effects of lncRNA XIST in RA were investigated when XIST expression was upregulated or downregulated in osteoblasts. TNF-α, IL-2, IL-6, alkaline phosphatase (ALP), osteocalcin, TGF-β1, and IGF1 were measured in vivo in RA rats.

resultsLncRNA XIST and STAT3 were expressed at high levels and let-7c-5p expressed at a low level in RA cartilage tissues. LncRNA XIST silencing or let-7c-5p enhancement led to decreased levels of TNF-α, IL-2, and IL-6, suggestive of suppressed inflammatory response, and increased levels of ALP, osteocalcin, TGF-β1, and IGF-1 as well as reduced damage in cartilage tissues.

conclusionLncRNA XIST downregulation could promote proliferation and differentiation of osteoblasts in RA, serving as a future therapeutic target for RA.

Indexed as

AdultAnimalsArthritis, RheumatoidCell DifferentiationCell ProliferationCells, CulturedFemaleHumansMaleMicroRNAsMiddle AgedOsteoblastsRatsRats, WistarRNA, Long NoncodingSTAT3 Transcription FactorMicroRNAsMIRNlet-7c microRNA, humanMIRNLET7 microRNA, ratRNA, Long NoncodingSTAT3 protein, humanStat3 protein, ratSTAT3 Transcription FactorXIST non-coding RNALet-7c-5plong non-coding RNA X-inactive specific transcriptosteoblastrheumatoid arthritissignal transducer and activator of transcription 3

Identifiers

PMID32881056
PMCPMC7676202
OpenAlexW3015135352

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.