Evidence map›Paper›PMID 25560389›Full record

ArticlePloS one2015

MiR-125a-3p regulates glioma apoptosis and invasion by regulating Nrg1.

Feng Yin, Jian Ning Zhang, Shu Wei Wang, Chun Hui Zhou, Ming Ming Zhao, Wen Hong Fan, Ming Fan, Shuang Liu

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Impact ofBiomolecules & biomedicine · 2024
    Article
  2. Article
  3. Comparison of MicroRNA Levels of 18-60-month-old Autistic Children with Those of Their Siblings and Controls.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2024
    Article
  4. Article
  5. Article
  6. Noncoding RNAs in apoptosis: identification and function.Turkish journal of biology = Turk biyoloji dergisi · 2022
    Review
  7. Review
  8. Article
  9. [Neuregulin 2 is highly expressed in glioma tissues to regulate glial fibrillary acidic protein expressionNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  10. Article
  11. Article
  12. Non-Coding RNAs and Brain Tumors: Insights Into Their Roles in Apoptosis.Frontiers in cell and developmental biology · 2021
    Review
  13. Article
  14. Article
  15. The permissive role of TCTP in PMJournal of translational medicine · 2020
    Article
  16. Article
  17. Article
  18. 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

8 authors.

Feng YinDepartment of Neurosurgery, the Chinese PLA Navy General Hospital, Beijing, 100048, China.
Jian Ning ZhangDepartment of Neurosurgery, the Chinese PLA Navy General Hospital, Beijing, 100048, China.
Shu Wei WangDepartment of Neurosurgery, the Chinese PLA Navy General Hospital, Beijing, 100048, China.
Chun Hui ZhouDepartment of Neurosurgery, the Chinese PLA Navy General Hospital, Beijing, 100048, China.
Ming Ming ZhaoDepartment of Neurosurgery, the Chinese PLA Navy General Hospital, Beijing, 100048, China.
Wen Hong FanDepartment of Brain Protection & Plasticity Research, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Ming FanDepartment of Brain Protection & Plasticity Research, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Shuang LiuDepartment of Neurosurgery, the Chinese PLA Navy General Hospital, Beijing, 100048, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study was designed to examine the functional role and mechanism of miR-125a-3p in glioma development. Quantitative RT-PCR was used to evaluate miR-125a-3p expression in 60 glioma cases of different malignant grades. Then, the clinic pathologic significance of miR-125a-3p expression was determined in combination with the prognosis of the patients. In addition, the effects and mechanisms of miR-125a-3p on the proliferation, apoptosis and invasion of glioma cells were further investigated. The results showed that the expression of miR-125a-3p was decreased significantly in most malignant glioma samples relative to normal brain tissues and glioma tissues of low-malignant degree. Further kaplan-meier survival analysis showed that the lower expression of miR-125a-3p was associated with a poor prognosis of GBM patients. Functional analysis showed that the reintroduction of miR-125a-3p into glioblastoma cell lines induces markedly the apoptosis and suppresses the proliferation and migration of glioblastoma cells in vitro and in vivo. Luciferase assay and Western blot analysis revealed that Nrg1 is a direct target of miR-125a-3p. Furthermore, an increased expression of Nrg1 could reverse the effects of overexpression of miR-125a-3p on the proliferation, apoptosis and migration of glioblastoma cells. These findings suggest that miR-125a-3p performed an important role in glioma development mediated by directly regulating the expression of Nrg1. This study also provides a potential target for diagnosis and treatment of malignant glioma.

Indexed as

3' Untranslated RegionsAnimalsApoptosisBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationFemaleGliomaHumansKaplan-Meier EstimateMiceMice, Inbred BALB CMice, NudeMicroRNAsNeoplasm Invasiveness3' Untranslated RegionsMicroRNAsMIRN125 microRNA, humanNeuregulin-1

Identifiers

PMID25560389
PMCPMC4283963

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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.