Evidence map›Paper›PMID 32892482›Full record

ArticleMolecular oncology2020

Interaction of BACH2 with FUS promotes malignant progression of glioma cells via the TSLNC8-miR-10b-5p-WWC3 pathway.

Yang Yang, Xiaobai Liu, Jian Zheng, Yixue Xue, Libo Liu, Jun Ma, Ping Wang, Chunqing Yang, Di Wang, Lianqi Shao and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Yang YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Xiaobai LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Jian ZhengDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Yixue XueDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Libo LiuDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Jun MaDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Ping WangDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Chunqing YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Di WangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Lianqi ShaoDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Xuelei RuanDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Yunhui LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.ORCID 0000-0002-3709-3226
China Medical University · CNLiaoning University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma, a common malignant tumour of the human central nervous system, has poor prognosis and limited treatment options. Dissecting the biological mechanisms underlying glioma pathogenesis can facilitate the development of better therapies. Here, we investigated the endogenous expression of BTB and CNC homolog 2 (BACH2), fused in sarcoma (FUS), TSLNC8 and microRNA (miR)-10b-5p in glioma cells and tissues. We studied the interaction between BACH2 and FUS and its contribution to glioma progression. We demonstrated that the interaction between BACH2 and FUS promoted glioma progression via transcriptional inhibition of TSLNC8. Overexpression of TSLNC8 restrained glioma progression by suppressing miR-10b-5p. Binding of TSLNC8 to miR-10b-5p attenuated the suppression of WWC family member 3 (WWC3) by miR-10b-5p and activated the Hippo signalling pathway. Growth of subcutaneous xenografts could be inhibited by knockdown of BACH2 or FUS, by overexpressing TSLNC8 or a combination of the three, also leading to a prolonged survival in nude mice. Our results indicate that the BACH2 and FUS/TSLNC8/miR-10b-5p/WWC3 axis is responsible for glioma development and could serve as a potential target for the development of new glioma therapies.

Indexed as

Signal TransductionAnimalsBasic-Leucine Zipper Transcription FactorsCell Line, TumorCentral Nervous System NeoplasmsDisease ProgressionGene Expression Regulation, NeoplasticGliomaHumansIntracellular Signaling Peptides and ProteinsMice, NudeMicroRNAsProtein Interaction MapsRNA-Binding Protein FUSRNA, Long NoncodingBACH2 protein, humanBasic-Leucine Zipper Transcription FactorsFUS protein, humanIntracellular Signaling Peptides and ProteinsMicroRNAsMIRN10 microRNA, humanRNA-Binding Protein FUSRNA, Long NoncodingWWC3 protein, humanBACH2FUSgliomamiR-10b-5pTSLNC8WWC3

Identifiers

PMID32892482
PMCPMC7607167
OpenAlexW3083587259

What OpenQuestion holds

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Registered trials

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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.