Evidence map›Paper›PMID 26893028›Full record

ArticleJournal of physiology and biochemistry2016

miR-92b regulates glioma cells proliferation, migration, invasion, and apoptosis via PTEN/Akt signaling pathway.

Hang Song, Yao Zhang, Na Liu, Chao Wan, Dongdong Zhang, Sheng Zhao, Yan Kong, Liudi Yuan

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of physiology and biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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  10. Role of MicroRNAs in Extreme Animal Survival Strategies.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Review
  12. Observational
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  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

8 authors at 1 institution in 1 country.

Hang SongState Education Ministry's Key Laboratory of Developmental Genes and Human Diseases, Southeast University, #2 Sipailou Road, Nanjing, 210096, China.
Yao ZhangState Education Ministry's Key Laboratory of Developmental Genes and Human Diseases, Southeast University, #2 Sipailou Road, Nanjing, 210096, China.
Na LiuState Education Ministry's Key Laboratory of Developmental Genes and Human Diseases, Southeast University, #2 Sipailou Road, Nanjing, 210096, China.
Chao WanState Education Ministry's Key Laboratory of Developmental Genes and Human Diseases, Southeast University, #2 Sipailou Road, Nanjing, 210096, China.
Dongdong ZhangState Education Ministry's Key Laboratory of Developmental Genes and Human Diseases, Southeast University, #2 Sipailou Road, Nanjing, 210096, China.
Sheng ZhaoDepartment of Biochemistry and Molecular Biology, Medical School of Southeast University, #87 Dingjiaqiao Road, Nanjing, 210009, China.
Yan KongDepartment of Biochemistry and Molecular Biology, Medical School of Southeast University, #87 Dingjiaqiao Road, Nanjing, 210009, China.
Liudi YuanState Education Ministry's Key Laboratory of Developmental Genes and Human Diseases, Southeast University, #2 Sipailou Road, Nanjing, 210096, China. yld@seu.edu.cn.
Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is a highly invasive malignant primary brain tumor with neoplastic growth. Despite the progresses made in surgery, chemotherapy, and radiation in recent decade, the prognosis of patients with gliomas remains poor and the average survival time of patients suffering from glioblastoma is still short. As a potential therapy strategy, microRNAs have been considered as new targets for possible cancer treatment. In this study, we found that the miR-92b inhibitors (miR-92b-I) could inhibit the proliferation, migration, invasion, and promote the apoptosis of glioma cells. As a predicted target of miR-92b, phosphatase and tensin homolog (PTEN), also elevated at both mRNA and protein levels. Moreover, the Akt phosphorylation was consistently inhibited. The rescue experiment with miR-92b and PTEN double knockdown resulted in partial reversion of miR-92b-I-induced phenotypes. Taken together, our findings indicated that miR-92b-I could restrain the proliferation, invasion, migration, and stimulate apoptosis of glioma cells by targeting PTEN/Akt signaling pathway. Further investigations will focus on antitumor effect of miR‑92b-I in glioma treatment.

Indexed as

3' Untranslated RegionsAntagomirsAntimetabolites, AntineoplasticApoptosisCell Line, TumorCell MovementCell ProliferationComputational BiologyGene Expression Regulation, NeoplasticGenes, ReporterGliomaHumansMicroRNAsMutationPhosphorylationProtein Processing, Post-Translational3' Untranslated RegionsAKT1 protein, humanAntagomirsAntimetabolites, AntineoplasticMicroRNAsMIRN92 microRNA, humanProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanRNA, MessengerRNA, NeoplasmAktCarcinogenesisGlioblastomasmiR-92bPTEN

Identifiers

PMID26893028
OpenAlexW2275972315

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.