Evidence map›Paper›PMID 30038507›Full record

ArticleOncoTargets and therapy2018

MicroRNA-384 inhibits proliferation migration and invasion of glioma by targeting at CDC42.

Gengshi Gu, Li Wang, Junchen Zhang, Hao Wang, Tan Tan, Guangning Zhang

Abstract read
In one paragraph

Article in OncoTargets and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. microRNA-1471 suppresses glioma cell growth and invasion by repressing metadherin expression.International journal of clinical and experimental pathology · 2018
    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.

Gengshi Gu *Department of Neurosurgery, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, People's Republic of China, zhangguangning2008@163.com; tantan19830610@163.com.
Li Wang *Department of Neurosurgery, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, People's Republic of China, zhangguangning2008@163.com; tantan19830610@163.com.
Junchen ZhangDepartment of Neurosurgery, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, People's Republic of China, zhangguangning2008@163.com; tantan19830610@163.com.
Hao WangDepartment of Clinical Laboratory, Chinese People's Liberation Army General Hospital, Beijing, 100700, People's Republic of China.
Tan TanDepartment of Neurosurgery, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, People's Republic of China, zhangguangning2008@163.com; tantan19830610@163.com.
Guangning ZhangDepartment of Neurosurgery, Affiliated Hospital of Jining Medical University, Jining, Shandong 272000, People's Republic of China, zhangguangning2008@163.com; tantan19830610@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccumulative evidence indicated that microRNAs (miRNAs) play a critical role in carcinogenesis and biological behaviors of glioma. Further bio-molecular mechanisms of miRNAs in glioma cells remain largely unknown, which can contribute to novel therapeutic strategy.

methodsIn the present study, we detected the expression level of miR-384 by RT-PCR and Western blot. Meanwhile, Gain and loss function assay of miR-384 by transfection of miR-384 mimics and inhibitor. Moreover, wild and mutant psiCHECK-2-CDC42-3'-UTR luciferase reporter vectors were constructed and transfected into glioma cells with miR-384 mimics or miR-NC.

resultsmiR-384 was dramatically down-regulated in human glioma tissues. It was also demonstrated that miR-384 significantly inhibited proliferation, migration and invasion of glioma cells. Cell division cycle 42 (Cdc42) was a direct target of miR-384 according to results of RT-PCR and Western blotting.

conclusionOur research demonstrated that miR-384 exerted an inhibitory effect on proliferation, migration and invasion of glioma via suppressing the expression of

Indexed as

CDC42gliomainvasionmiR-384proliferation

Identifiers

PMID30038507
PMCPMC6052920

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.