Evidence map›Paper›PMID 33488865›Full record

ArticleArchives of medical science : AMS2021

MicroRNA-101 inhibits growth and metastasis of human ovarian cancer cells by targeting PI3K/AKT.

Min Wei, Hongjuan Jin, ShuLi Yang, Zhuo Li, Xinlei Wang, LiXiang Li, Yan Jia, ManHua Cui

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Tumor Cell-Derived Exosomal miR-770 Inhibits M2 Macrophage PolarizationFrontiers in cell and developmental biology · 2021
    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

8 authors at 2 institutions in 1 country.

Min WeiDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
Hongjuan JinDepartment of Plastic and Reconstructive Surgery, The First Hospital of Jilin University, Changchun, Jilin, China.
ShuLi YangDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
Zhuo LiDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
Xinlei WangDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
LiXiang LiDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
Yan JiaDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
ManHua CuiDepartment of Gynecology and Obstetrics, The Second Hospital of Jilin University, Changchun, Jilin, China.
Second Affiliated Hospital of Jilin University · CNFirst Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOvarian cancer is the most frequent cause of gynecological cancer related mortality in woman. This study was designed to investigate the role and therapeutic potential of miRNA-101 in ovarian cancer. MATERIAL AND

methodsExpression analysis was carried out by real-time quantitative polymerase chain reaction. Transfections were performed with the help of Lipofectamine 2000 reagent. AO/EB and annexin V/PI staining was used to detect apoptosis and flow cytometry was used for cell cycle analysis. Western blotting was employed for cell cycle analysis.

resultsIt was found that miRNA-101 was significantly down-regulated in ovarian cancer cells. The over-expression of miRNA-101 causes a significant decrease in the viability of ovarian cancer cells via the initiation of apoptosis and sub-G1 arrest of OVACAR-3 cells. It was indicated that PTEN was the potential target of miRNA-101 in OVACAR-3 cells. There was 4.5-fold up-regulation of PTEN expression in ovarian cancer cell lines and the over-expression of miRNA-101 in OVACAR-3 cells resulted in the down-regulation of PTEN expression. The inhibition of PTEN in the OVACAR-3 cells arrested the proliferation of these cells. The over-expression of miRNA-101 causes significant down-regulation in PI3K and AKT expression of OVACAR-3 cells.

conclusionsIt can be concluded that miRNA-101 acts as a tumor suppressor which may be beneficial in the treatment of ovarian cancer.

Indexed as

apoptosismicroRNAovarian cancerproliferation

Identifiers

PMID33488865
PMCPMC7811304
OpenAlexW2954243182

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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.