Evidence map›Paper›PMID 33372387›Full record

ArticleJournal of cellular and molecular medicine2021

LINC01116 promotes proliferation and migration of endometrial stromal cells by targeting FOXP1 via sponging miR-9-5p in endometriosis.

Liangyi Cui, Silei Chen, Dandan Wang, Qing Yang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Liquid Biopsy in Endometriosis: A Systematic Review.International journal of molecular sciences · 2023
    Pooled it
  2. Article
  3. Review
  4. Review
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  7. Review
  8. Trace elements and metal nanoparticles: mechanistic approaches to mitigating chemotherapy-induced toxicity-a review of literature evidence.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2024
    Review
  9. Review
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  16. Corrigendum.Journal of cellular and molecular medicine · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. The Role of Long Non-Coding RNAs in Endometriosis.International journal of molecular sciences · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Liangyi CuiDepartment of Obstetrics & Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID 0000-0003-4953-9552
Silei ChenDepartment of Obstetrics & Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.
Dandan WangDepartment of Obstetrics & Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.
Qing YangDepartment of Obstetrics & Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID 0000-0002-6379-7577
China Medical University · CN

Funding

Key Research and Development Guidance Plan of Liaoning Province 2018225062National Natural Science Foundation of China 81872125the Local Technology and Development Key Program of Liaoning Province 2019416020
6 · The paper itself

Abstract

Endometriosis is a common multi-factorial gynaecological disease. Recent studies have revealed that long non-coding RNAs (lncRNAs) are involved in the pathogenesis of endometriosis. In the present study, the expression profiles of lncRNAs in 6 pairs of endometriosis ectopic endometrium (ecEM) and eutopic endometrium (euEM) tissues were analysed by RNA sequencing. From the profiles, LINC01116 was found to be up-regulated in ecEM tissues compared to euEM tissues and was verified by quantitative real-time PCR (qRT-PCR). Then, functional experiments demonstrated that LINC01116 promoted the proliferation and migration of ectopic primary endometrial stromal cells (ESCs), while miR-9-5p exerted the opposite effects. Dual-luciferase reporter assays verified that LINC01116 directly sponged miR-9-5p and relieved the suppression of its target, Forkhead box protein P1 (FOXP1). Rescue experiments further demonstrated that LINC01116 could promote proliferation and migration of ESCs by targeting FOXP1 via sponging miR-9-5p. Overall, our study illuminates that LINC01116 promotes the progression of endometriosis through the miR-9-5p/FOXP1 axis. This finding provides a novel therapeutic target for patients with endometriosis.

Indexed as

Gene Expression RegulationRNA InterferenceAdultCell MovementCell ProliferationComputational BiologyDisease SusceptibilityEndometriosisFemaleForkhead Transcription FactorsGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansMicroRNAsRepressor ProteinsStromal CellsForkhead Transcription FactorsFOXP1 protein, humanMicroRNAsMIRN92 microRNA, humanRepressor ProteinsceRNAendometriosisFOXP1LINC01116miR-9-5p

Identifiers

PMID33372387
PMCPMC7882988
OpenAlexW3115408500

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.