Evidence map›Paper›PMID 27896672›Full record

ArticleHormones & cancer2017

miR-15b Inhibits the Progression of Glioblastoma Cells Through Targeting Insulin-like Growth Factor Receptor 1.

Jian Wang, Huaqiang Liu, Lin Tian, Fachen Wang, Liangbo Han, Wei Zhang, Yun-An Bai

Open access · greenAbstract read
In one paragraph

Article in Hormones & cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
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  5. MiR-21 participates in LPS-induced myocardial injury by targeting Bcl-2 and CDK6.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Critical role of HOX transcript antisense intergenic RNA (HOTAIR) in gliomas.Journal of molecular medicine (Berlin, Germany) · 2020
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
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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

7 authors at 1 institution in 1 country.

Jian WangDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China.
Huaqiang LiuDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China.
Lin TianDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China.
Fachen WangDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China.
Liangbo HanDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China.
Wei ZhangDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China.
Yun-An BaiDepartment of Neurosurgery, Weifang Yidu Central Hospital, No. 4138, Linglongshan Road, Qingzhou, Shandong, 262500, China. baiyayidu@163.com.
Yidu Central Hospital of Weifang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The microRNAs (miRNAs) have been suggested as a tumor suppressor in recent years. miR-15b was reported to exert an anti-oncogenic role in the proliferation, migration, and invasion of diverse tumor cells. However, the mechanisms underlying miR-15b-mediated biology of glioblastoma are still unclear. In the present study, the expression of miR-15b was down-regulated in glioblastoma tumor tissues and U87 and U251 cells, but insulin-like growth factor receptor 1 (IGF1R) expression became up-regulated in these tumor tissues and cells (all p < 0.001). Furthermore, IGF1R expression was inversely associated with miR-15b expression. Notably, patients with lower miR-15b expression have a much shorter survival period compared with high expression (log-rank test p = 0.045). In vitro data demonstrated that miR-15b mimics inhibited the proliferation, cell cycle arrest, and invasion of U87 and U251 cells. Besides, we validated IGF1R as a direct target of miR-15b using dual luciferase assays, and IGF1R plasmids partially abrogated miR-15b mimics inhibited cell proliferation. In vivo, miR-15b mimics indeed repressed cell proliferation in mouse xenograft model. In conclusion, our study demonstrated that miR-15b inhibits the progression of glioblastoma cells through targeting IGF1R, and miR-15b can be recommended as a tumor suppressor in the progression of glioblastoma.

Indexed as

AnimalsCell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticGenes, Tumor SuppressorGlioblastomaHumansMaleMiceMice, Inbred BALB CMice, NudeMicroRNAsReceptor, IGF Type 1Receptors, SomatomedinUp-RegulationIGF1R protein, humanMicroRNAsMIRN15 microRNA, humanReceptor, IGF Type 1Receptors, SomatomedinGlioblastomaIGF1RmiR-15b

Identifiers

PMID27896672
PMCPMC10355966
OpenAlexW2558754810

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.