Evidence map›Paper›PMID 27520092›Full record

ArticleJournal of physiology and biochemistry2016

Let-7b inhibits the malignant behavior of glioma cells and glioma stem-like cells via downregulation of E2F2.

Hang Song, Yao Zhang, Na Liu, Dongdong Zhang, Chao Wan, 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 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 60 citations in OpenAlex.

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  15. Cancers · 2021
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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 SongThe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, No. 2 Sipailou Road, Nanjing, Jiangsu Province, 210096, China.
Yao ZhangThe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, No. 2 Sipailou Road, Nanjing, Jiangsu Province, 210096, China.
Na LiuThe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, No. 2 Sipailou Road, Nanjing, Jiangsu Province, 210096, China.
Dongdong ZhangThe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, No. 2 Sipailou Road, Nanjing, Jiangsu Province, 210096, China.
Chao WanThe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, No. 2 Sipailou Road, Nanjing, Jiangsu Province, 210096, China.
Sheng ZhaoDepartment of Biochemistry and Molecular Biology, Medical School of Southeast University, No. 87 Dingjiaqiao Road, Nanjing, Jiangsu Province, 210009, China.
Yan KongDepartment of Biochemistry and Molecular Biology, Medical School of Southeast University, No. 87 Dingjiaqiao Road, Nanjing, Jiangsu Province, 210009, China.
Liudi YuanThe Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, No. 2 Sipailou Road, Nanjing, Jiangsu Province, 210096, China. yld@seu.edu.cn.
Southeast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM), the most common and lethal primary brain tumor in adults characterized by high proliferative ability and mortality rate, contains a small subpopulation of cancer stem-like cells (CSCs), which is responsible for GBM progression and therapeutic resistance. Numerous microRNAs are strongly implicated in the malignancy of glioma. However, their specific functions and roles have yet to be fully demonstrated. In the present study, we revealed that the upregulation of Let-7b, a member of the Let-7 microRNA family, inhibited proliferation, migration, and invasion in glioma cell lines. Using bioinformatics, expression analysis, and luciferase assay, E2F2 was confirmed as a candidate target of Let-7b. Moreover, we also observed that elevated levels of Let-7b resulted in a reduction of tumor sphere growth and stemness of glioma stem-like cells. Furthermore, we found that knockdown of E2F2 expression could reduce the proliferation of glioma and GSCs, while overexpression of E2F2 partially abrogated the inhibitory effect of Let-7b on the proliferation of glioma and GSCs. In conclusion, we suggest that Let-7b could be developed into a promising anticancer target in glioma.

Indexed as

Gene Expression Regulation, NeoplasticBase SequenceBinding SitesCell Line, TumorCell MovementCell ProliferationComputational BiologyE2F2 Transcription FactorGenes, ReporterHumansLuciferasesMicroRNAsNeoplastic Stem CellsNeurogliaRNA, Small InterferingSignal TransductionE2F2 protein, humanE2F2 Transcription FactorLuciferasesMicroRNAsmirnlet7 microRNA, humanRNA, Small InterferingE2F2GliomaGlioma stem cellLet-7bmiRNA

Identifiers

PMID27520092
OpenAlexW2508109637

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.