Evidence map›Paper›PMID 32779991›Full record

ArticleBioengineered2020

ELFN1-AS1 accelerates cell proliferation, invasion and migration via regulating miR-497-3p/CLDN4 axis in ovarian cancer.

Youkun Jie, Lu Ye, He Chen, Xiaohong Yu, Li Cai, Wenfeng He, Yonghui Fu

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Article
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  13. International journal of molecular sciences · 2023
    Review
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  15. Article
  16. Claudin-4: A New Molecular Target for Epithelial Cancer Therapy.International journal of molecular sciences · 2023
    Review
  17. lncRNAActa biochimica et biophysica Sinica · 2023
    Article
  18. Long non-coding RNAs involved in retinoblastoma.Journal of cancer research and clinical oncology · 2023
    Review
  19. The Theory ofGenes · 2022
    Article
  20. Prognostic analysis ofAnnals of translational medicine · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Youkun JieDepartment of Pathology, Jiangxi Maternal and Child Health Hospital , Nanchang, Jiangxi, China.
Lu YeDepartment of Pathology, Jiangxi Maternal and Child Health Hospital , Nanchang, Jiangxi, China.
He ChenJiangxi Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University , Nanchang, Jiangxi, China.
Xiaohong YuDepartment of Pathology, Jiangxi Maternal and Child Health Hospital , Nanchang, Jiangxi, China.
Li CaiDepartment of Oncology, Jiangxi Maternal and Child Health Hospital , Nanchang, Jiangxi, China.
Wenfeng HeJiangxi Key Laboratory of Molecular Medicine, The Second Affiliated Hospital of Nanchang University , Nanchang, Jiangxi, China.
Yonghui FuDepartment of Psychiatry, Jiangxi Mental Hospital/Affiliated Mental Hospital of Nanchang University , Nanchang, Jiangxi, China.
Jiangxi Maternal and Child Health Hospital · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies indicated that long non-coding RNAs (LncRNAs) were involved in the progression of multiple cancers including ovarian cancer (OV). LncRNA ELFN1-AS1 functioned as an oncogene in many cancers, but its potential roles in OV were largely unclear. In the current study, we were aimed at clarifying the biological roles and molecular mechanisms of ELFN1-AS1 in OV. We found that ELFN1-AS1 was significantly upregulated in OV tissues and cell lines. High expression of ELFN1-AS1 was associated with poor prognosis in OV patients. Knockdown of ELFN1-AS1 inhibited the proliferation, migration and invasion of SKOV3 cell lines and repressed tumor growth in xenografted ovarian models. Mechanistically, ELFN1-AS1 promoted the proliferation, migration and invasion of SKOV3 cells by sponging miR-497-3p. Additionally, CLDN4 was verified to be the target of miR-497-3p. Rescue experiments revealed that miR-497-3p inhibition could partly reverse the inhibitory effect of ELFN1-AS1 silencing on proliferation, migration and invasion of SKOV3 cell lines. Taken together, our findings indicated that ELFN1-AS1 acted as an oncogene in ovarian cancer through regulating the expression of CLDN4 by directly interacting with miR-497-3p. The results suggested that ELFN1-AS1 might act as a promising therapeutic target for OV.

Indexed as

Cell LineCell Line, TumorCell MovementCell ProliferationClaudin-3Claudin-4Disease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsNerve Tissue ProteinsOvarian NeoplasmsReverse Transcriptase Polymerase Chain ReactionClaudin-3Claudin-4CLDN4 protein, humanELFN1 protein, humanMicroRNAsMIRN497 microRNA, humanNerve Tissue ProteinsCLDN4ELFN1-AS1miR-497-3povarian cancer

Identifiers

PMID32779991
PMCPMC8291874
OpenAlexW3048629563

What OpenQuestion holds

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Registered trials

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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.