Evidence map›Paper›PMID 27615604›Full record

ArticleScientific reports2016

miR-224-3p inhibits autophagy in cervical cancer cells by targeting FIP200.

Wang Fang, Shan Shu, Li Yongmei, Zhu Endong, Yin Lirong, Sun Bei

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.7field-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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
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  10. Review
  11. Virus, Exosome, and MicroRNA: New Insights into Autophagy.Advances in experimental medicine and biology · 2022
    Article
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  15. The Emerging Roles of Autophagy-Related MicroRNAs in Cancer.International journal of biological sciences · 2021
    Review
  16. Article
  17. Review
  18. Autophagy in cancers including brain tumors: role of MicroRNAs.Cell communication and signaling : CCS · 2020
    Review
  19. Article
  20. Article
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

6 authors at 2 institutions in 1 country.

Wang FangThe Second Hospital of Tianjin Medical University, 300070 Tianjin, China.
Shan ShuThe Second Hospital of Tianjin Medical University, 300070 Tianjin, China.
Li YongmeiDepartment of Medical Microbiology, School of Basic Medical Sciences, Tianjin Medical University, 300070 Tianjin, China.
Zhu EndongKey Laboratory of Hormones and Development (Ministry of Health), Metabolic Diseases Hospital &Tianjin Institute of Endocrinology, Department of physiology, Tianjin Medical University, 300070 Tianjin, China.
Yin LirongThe Second Hospital of Tianjin Medical University, 300070 Tianjin, China.
Sun BeiKey Laboratory of Hormones and Development (Ministry of Health), Metabolic Diseases Hospital &Tianjin Institute of Endocrinology, Department of physiology, Tianjin Medical University, 300070 Tianjin, China.
Tianjin Medical University · CNSecond Hospital of Tianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CC) is a malignant solid tumor, which is one of the main causes of morbidity and mortality in women. Persistent High-risk human papillomavirus (hrHPV) infection is closely related to cervical cancer and autophagy has been suggested to inhibit viral infections. miRNAs have been reported to regulate autophagy in many solid tumors with many studies implicating miR-224-3p in the regulation of autophagy. In this study, we performed a miRNA microarray analysis on CC tissues and found that a large number of miRNAs with differential expressions in hrHPV-infected tissues. We identified miR-224-3p as a candidate miRNA selectively up regulated in HPV-infected tissues and cell lines. Further analysis revealed that miR-224-3p regulates autophagy in cervical cancer tissues and cell lines. While the overexpression of miR-224-3p inhibits autophagy in HPV-infected cells, knocking down endogenous miR-224-3p increases autophagy activity in the same cells. In addition, we found that miR-224-3p directly inhibits the expression of autophagy related gene, FAK family-interacting protein of 200 kDa (FIP200). In summary, we found that miR-224-3p regulates autophagy in hrHPV-induced cervical cancer cells through targeting FIP200 expression.

Indexed as

Autophagy3' Untranslated RegionsAutophagy-Related ProteinsBase SequenceBinding SitesFemaleGene ExpressionGene Expression Regulation, NeoplasticHeLa CellsHumansMicroRNAsPapillomavirus InfectionsProtein-Tyrosine KinasesRNA InterferenceUterine Cervical Neoplasms3' Untranslated RegionsAutophagy-Related ProteinsMicroRNAsMIRN224 microRNA, humanProtein-Tyrosine KinasesRB1CC1 protein, human

Identifiers

PMID27615604
PMCPMC5018969
OpenAlexW2519608228

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.