Evidence map›Paper›PMID 31815639›Full record

ArticleJournal of ovarian research2019

miR-552 promotes ovarian cancer progression by regulating PTEN pathway.

Wenman Zhao, Tao Han, Bao Li, Qianyun Ma, Pinghua Yang, Hengyu Li

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 72 citations in OpenAlex.

  1. The cross-talk between GSK-3β, RKIP, and PTEN as potential targets for therapeutic implications in cancer: a comprehensive insight.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
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  4. How MicroRNAs Command the Battle against Cancer.International journal of molecular sciences · 2024
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  8. Cancer resistance via the downregulation of the tumor suppressorsExploration of targeted anti-tumor therapy · 2023
    Review
  9. Integration of TE Induces Cancer Specific Alternative Splicing Events.International journal of molecular sciences · 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

6 authors at 4 institutions in 1 country.

Wenman ZhaoDepartment of General surgery, Cao county people's hospital, East of Qinghe Road, Heze, 274400, Shandong province, China. cxrmyyzwm@126.com.
Tao HanDepartment of Oncology, General Hospital of Northern Theater Command, Shenyang, 110016, Liaoning Province, China.
Bao LiDepartment of General surgery, Cao county people's hospital, East of Qinghe Road, Heze, 274400, Shandong province, China.
Qianyun MaDepartment of Urology surgery, First Affiliated Hospital of Second Military Medical University, Shanghai, 200433, China.
Pinghua YangDepartment of Biliary Tract Surgery, Third Affiliated Hospital of Second Military Medical University, Shanghai, 200438, China. yangpinghua2008@163.com.
Hengyu LiDepartment of Breast and Thyroid surgery, First Affiliated Hospital of Second Military Medical University, Shanghai, 200433, China. lhy@smmu.edu.cn.ORCID http://orcid.org/0000-0001-8354-2224
Second Military Medical University · CNArmy Medical University · CNBoxing People's Hospital · CNGeneral Hospital of Shenyang Military Region · CN

Funding

China Postdoctoral Science Foundation 2014M552624the National Natural Science Foundation of Shanghai 1438600the National Natural Science Foundation of Shanghai 19ZR1400300
6 · The paper itself

Abstract

backgroundIncreasing researches have demonstrated the critical functions of MicroRNAs (miRNAs) in the progression of malignant tumors, including ovarian cancer. It was reported that miR-552 was an important oncogene in both breast cancer and colorectal cancer. However, the role of miR-552 in ovarian cancer (OC) remains to be elucidated.

methodsRT-PCR and western blot analysis were used to detect the expression of miR-552 and PTEN. The impact of miR-552 on ovarian cancer proliferation and metastasis was investigated in vitro. The prognostic value of miR-552 was evaluated using the online bioinformatics tool Kaplan-Meier plotter.

resultsIn the present study, we for first found that miR-552 was upregulated in ovarian cancer, especially in metastatic and recurrence ovarian cancer. Forced miR-552 expression promotes the growth and metastasis of ovarian cancer cells. Consistently, miR-552 interference inhibits the proliferation and metastasis of ovarian cancer cells. Mechanically, bioinformatics and luciferase reporter analysis identified Phosphatase and tension homolog (PTEN) as a direct target of miR-552. miR-552 downregulated the PTEN mRNA and protein expression in ovarian cancer cells. Furthermore, the PTEN siRNA abolishes the discrepancy of growth and metastasis capacity between miR-552 mimic ovarian cells and control cells. More importantly, upregulation of miR-552 predicts the poor prognosis of ovarian cancer patients.

conclusionOur findings revealed that miR-552 could promote ovarian cancer cells progression by targeting PTEN signaling and might therefore be useful to predict patient prognosis.

Indexed as

Cell Line, TumorCell MovementDisease ProgressionFemaleHumansMicroRNAsMiddle AgedNeoplasm Recurrence, LocalOvarian NeoplasmsPTEN PhosphohydrolaseSignal TransductionMicroRNAsMIRN552 microRNA, humanPTEN PhosphohydrolasePTEN protein, humanMetastasismiR-552Ovarian cancerProliferationPTEN

Identifiers

PMID31815639
PMCPMC6900846
OpenAlexW2992277018

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.