Evidence map›Paper›PMID 32398968›Full record

ArticleCancer cell international2020

FENDRR suppresses cervical cancer proliferation and invasion by targeting miR-15a/b-5p and regulating TUBA1A expression.

Yunheng Zhu, Xiaohua Zhang, Lifeng Wang, Xiuxiang Zhu, Ziyin Xia, Ling Xu, Jun Xu

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
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  5. lncRNA FENDRR Predicts Adverse Prognosis and Regulates the Development of Esophageal Squamous Cell Carcinoma Through Negatively Modulating miR-495-3p.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
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  8. Review
  9. Review
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  11. Journal of Cancer · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. LncRNA FENDRR Suppresses Melanoma Growth via Influencing c-Myc mRNA Level.Clinical, cosmetic and investigational dermatology · 2023
    Article
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  17. Article
  18. Article
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  20. Review
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.

Yunheng Zhu *1Department of Obstetrics and Gynecology, Minhang Hospital, Fudan University, No.170 Xinsong Road, Minhang District, Shanghai, 201199 China.
Xiaohua Zhang *Minhang District Maternal and Child Health Hospital, Shanghai, 201102 China.
Lifeng Wang1Department of Obstetrics and Gynecology, Minhang Hospital, Fudan University, No.170 Xinsong Road, Minhang District, Shanghai, 201199 China.
Xiuxiang Zhu1Department of Obstetrics and Gynecology, Minhang Hospital, Fudan University, No.170 Xinsong Road, Minhang District, Shanghai, 201199 China.
Ziyin Xia1Department of Obstetrics and Gynecology, Minhang Hospital, Fudan University, No.170 Xinsong Road, Minhang District, Shanghai, 201199 China.
Ling Xu1Department of Obstetrics and Gynecology, Minhang Hospital, Fudan University, No.170 Xinsong Road, Minhang District, Shanghai, 201199 China.ORCID 0000-0002-9456-9390
Jun Xu1Department of Obstetrics and Gynecology, Minhang Hospital, Fudan University, No.170 Xinsong Road, Minhang District, Shanghai, 201199 China.
Fudan University · CNPudong Maternal and Child Health Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious literature has revealed long non-coding RNAs (lncRNAs) are crucial regulators for cell functions and gene expression. LncRNA fetal-lethal non-coding developmental regulatory RNA (FENDRR) was reported as a biological suppressor in several types of human cancers, yet relevant mechanisms and biological effects of FENDRR with regards to cervical cancer (CC) are not explored until now.

methodsIn this study, quantitative real-time polymerase chain reaction (qRT-PCR) analysis detected gene expression in tissues and cells. Gain- or loss-of-function experiments revealed the biological effects of FENDRR and miR-15a/b-5p on CC cell functions. Bioinformatics tools were used to predict the relevant genes. Mechanism experiments including RNA immunoprecipitation (RIP) assay, pull down assay and luciferase reporter assay depicted the binding situation and coexistence of indicated genes.

resultsFENDRR was downregulated in CC tissues and cells, which suppressed CC progression. MiR-15a-5p and miR-15b-5p shared binding sites with FENDRR and had interaction with FENDRR. Tubulin alpha1A (TUBA1A) was downregulated in CC tissues and positively modulated by FENDRR. TUBA1A was the target of miR-15a/b-5p. TUBA1A silencing rescued the effect of FENDRR overexpression on CC cell growth and migration.

conclusionFENDRR inhibits CC progression through upregulating TUBA1A in a miR-15a/b-5p-dependent manner.

Indexed as

Cervical cancerFENDRRmiR-15a/b-5pTUBA1A

Identifiers

PMID32398968
PMCPMC7204253
OpenAlexW3022241110

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LicenceCC BY
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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.