Evidence map›Paper›PMID 29497031›Full record

ArticleCell death & disease2018

WW domain-binding protein 2 acts as an oncogene by modulating the activity of the glycolytic enzyme ENO1 in glioma.

Shuai Chen, Ya Zhang, Han Wang, Yu-Ying Zeng, Zhi Li, Ming-Li Li, Fang-Fang Li, Jun You, Zhi-Ming Zhang, Chi-Meng Tzeng

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 75 citations in OpenAlex.

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  20. The essential roles of mJournal of experimental & clinical cancer research : CR · 2022
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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

10 authors at 3 institutions in 2 countries.

Shuai ChenTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Ya ZhangTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Han WangTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Yu-Ying ZengDepartment of Breast Surgery, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Zhi LiTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Ming-Li LiTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Fang-Fang LiTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Jun YouDepartment of Breast Surgery, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, 361005, P.R. China.
Zhi-Ming ZhangDepartment of Breast Surgery, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, 361005, P.R. China. zhangzhiming164@aliyun.com.
Chi-Meng TzengTranslational Medicine Research Center (TMRC), School of Pharmaceutical Science, Xiamen University, Xiamen, Fujian, 361005, P.R. China. cmtzeng@xmu.edu.cn.
Xiamen University · CNFirst Affiliated Hospital of Xiamen University · CNTheranostics (New Zealand) · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

WW domain-binding protein 2 (WBP2) has been demonstrated as oncogenic in breast cancer. Many studies have revealed the WBP2 gene as a high-risk gene for leukoariaosis and cerebral white matter lesions is important in the pathologic stage of glioma development. This study aimed to illustrate the underlying mechanism by which WBP2 regulates the process of glioma development. The expression pattern of WBP2 in several tumor cells was determined, clarifying the carcinogenic action of WBP2 in glioma cells. Overexpression of WBP2 in glioma cells promoted cell proliferation and migration, and the number of S-phase cells, whereas the depletion of WBP2 by RNAi-mediated knockdown restrained cell growth and cell cycle progression. Upregulation of WBP2 significantly enhanced the tumorigenic ability of U251 cells in vivo. MS/GST pulldown assay identified α-enolase (ENO1) and Homer protein homolog 3 (Homer3) as novel potent interaction partners of WBP2. Knockdown of ENO1 or Homer3 allowed cell growth and migration to return to normal levels. Furthermore, in vitro and in vivo experiments indicated that the oncogenic role of WBP2 in glioma was through modulating ENO1 and glycolysis activity via the ENO1-PI3K/Akt signaling pathway. Collectively, these results reveal that WBP2 plays a vital role in the occurrence and development of glioma, indicating a target gene for glioblastoma treatment.

Indexed as

Adaptor Proteins, Signal TransducingAdultAgedAged, 80 and overAnimalsBiomarkers, TumorBrain NeoplasmsCell CycleCell MovementCell ProliferationDNA-Binding ProteinsFemaleGliomaGlycolysisHomer Scaffolding ProteinsHumansAdaptor Proteins, Signal TransducingBiomarkers, TumorDNA-Binding ProteinsENO1 protein, humanHOMER3 protein, humanHomer Scaffolding ProteinsPhosphopyruvate HydrataseTrans-ActivatorsTumor Suppressor ProteinsWBP2 protein, human

Identifiers

PMID29497031
PMCPMC5832848
OpenAlexW2790916173

What OpenQuestion holds

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LicenceCC BY
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.