Evidence map›Paper›PMID 29316313›Full record

ArticleCNS neuroscience & therapeutics2018

MicroRNA-21 promotes glioma cell proliferation and inhibits senescence and apoptosis by targeting SPRY1 via the PTEN/PI3K/AKT signaling pathway.

Chang Chai, Lai-Jun Song, Shuang-Yin Han, Xi-Qing Li, Ming Li

RetractedAbstract readRetracted Publication
In one paragraph

Article in CNS neuroscience & therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.3field-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

56 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
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  10. Expression analysis of human glioma susceptibility gene andAnnals of translational medicine · 2023
    Article
  11. Article
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  13. Review
  14. Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Chang ChaiHenan Eye Institute, Henan Provincial People's Hospital, Zhengzhou, China.
Lai-Jun SongDepartment of Neurosurgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Shuang-Yin HanDepartment of Gastroenterology, Henan Provincial People's Hospital, Zhengzhou, China.
Xi-Qing LiDepartment of Oncology, Henan Provincial People's Hospital, Zhengzhou, China.
Ming LiDepartment of Neurosurgery, Henan Provincial People's Hospital, Zhengzhou, China.ORCID 0000-0002-6440-4384
Henan Provincial People's Hospital · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsOur study aims to investigate the effect of microRNA-21 (miR-21) on the proliferation, senescence, and apoptosis of glioma cells by targeting SPRY1 via the PTEN/PI3K/AKT signaling pathway.

methodsGlioma tissues and brain tissues were collected for this study after surgical decompression for traumatic brain injury. RT-qPCR was employed to measure mRNA levels of miR-21, SPRY1, PTEN, PI3K, and AKT, and Western blotting was conducted to determine protein levels of SPRY1, PTEN, PI3K, AKT, p-AKT, Caspase-3, Caspase-9, P53, GSK3, and p-GSK3. Human glioma U87 cells were assigned into the blank, negative control (NC), miR-21 mimics, miR-21 inhibitors, siRNA-SPRY1, and miR-21 inhibitors + siRNA-SPRY1 groups, with human HEB cells serving as the normal group. Cell proliferation, cell cycle, and apoptosis were determined by MTT and flow cytometry, respectively.

resultsCompared with control group, an increased expression of miR-21, PI3K, AKT, p-AKT, P53, and p-GSK3, and a decreased expression of SPRY1, PTEN, Caspase-3, and Caspase-9 were observed in the glioma group, and no significant differences were found in the expression of GSK3. SPRY1 was verified to be the target gene of miR-21. Compared with the blank and NC groups, levels of PI3K, AKT, p-AKT, P53, and p-GSK3 increased while levels of SPRY1, PTEN, Caspase-3, and Caspase-9 decreased in the miR-21 mimics and siRNA-SPRY1 groups; the miR-21 inhibitors group reversed the tendency; furthermore, the miR-21 inhibitors group showed decreased cell proliferation but promoted apoptosis, which were opposite to the results of the miR-21 mimics and siRNA-SPRY1 groups.

conclusionMicroRNA-21 might promote cell proliferation and inhibit cell senescence and apoptosis of human glioma cells by targeting SPRY1 via the PTEN/PI3K/AKT signaling pathway.

Indexed as

AdolescentAdultAgedApoptosisBrainBrain NeoplasmsCell CycleCell Line, TumorCell ProliferationCellular SenescenceFemaleGliomaHumansMaleMembrane ProteinsMicroRNAsMembrane ProteinsMicroRNAsMIRN21 microRNA, humanPhosphatidylinositol 3-KinasesPhosphoproteinsProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanSPRY1 protein, humanapoptosiscell senescencegliomamicroRNA-21PTEN/PI3K/AKT signaling pathwaySprouty1

Identifiers

PMID29316313
PMCPMC6489721
OpenAlexW2782704938

What OpenQuestion holds

Textmetadata
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.