Evidence map›Paper›PMID 31431517›Full record

ArticleBioscience reports2019

Up-regulated ENO1 promotes the bladder cancer cell growth and proliferation via regulating β-catenin.

Mingfei Ji, Zhijun Wang, Jie Chen, Liqiong Gu, Ming Chen, Yelei Ding, Tao Liu

Expression of concernErratum issuedOpen access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. ENO1 and Cancer.Molecular therapy oncolytics · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Enolase 1, a Moonlighting Protein, as a Potential Target for Cancer Treatment.International journal of biological sciences · 2021
    Review
  17. Article
  18. Article
  19. Prognostic Value of Enolase Gene Family in Colon Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Mingfei JiDepartment of Urology, Changzheng Hospital, The Second Military Medical University, Shanghai, China.
Zhijun WangDepartment of Urology, Changzheng Hospital, The Second Military Medical University, Shanghai, China.
Jie ChenDepartment of Urology, Changzheng Hospital, The Second Military Medical University, Shanghai, China rexcj8298@163.com.ORCID 0000-0002-0975-5923
Liqiong GuDepartment of Ophthalmology, Shanghai East Hospital, Tongji University, Shanghai, China.
Ming ChenDepartment of Urology, Changzheng Hospital, The Second Military Medical University, Shanghai, China.
Yelei DingDepartment of Urology, Changzheng Hospital, The Second Military Medical University, Shanghai, China.
Tao LiuDepartment of Urology, Changzheng Hospital, The Second Military Medical University, Shanghai, China.
Second Military Medical University · CNShanghai East Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer (BC) is the ninth most common malignancy throughout the world. The molecular mechanisms of this disease remain largely unclear. The glycolytic enzyme enolase 1 (ENO1) has been shown to regulate the development of various cancers. However, the significance of ENO1 in BC is underdetermined. In this study, we found that ENO1 was highly expressed in BC tissues and cells. High expression of ENO1 was associated with the poor survival of BC patients. Using lentivirus-mediated knockdown and over-expression, we revealed that ENO1 was critical for the growth and proliferation of BC cells. ENO1 over-expression also promoted the proliferation of SV-HUC-1 cells. At the molecular level, the cell cycle and apoptosis related genes were regulated by ENO1. β-catenin expression was positively regulated by ENO1. Furthermore, ectopic expression of β-catenin reversed the effect of ENO1 knockdown on T24 cell proliferation and growth. Opposite results were observed in β-catenin knockdown T24 cells. Our findings suggested that ENO1 functioned as an oncogene in BC through regulating cell cycle, apoptosis and β-catenin. Targeting ENO1/β-catenin cascade may benefit for BC patients.

Indexed as

Apoptosisbeta CateninBiomarkers, TumorCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationDNA-Binding ProteinsHumansPhosphopyruvate HydrataseRNA InterferenceRNA, Small InterferingTumor Suppressor ProteinsUp-RegulationUrinary Bladder Neoplasmsbeta CateninBiomarkers, TumorDNA-Binding ProteinsENO1 protein, humanPhosphopyruvate HydrataseRNA, Small InterferingTumor Suppressor Proteinsapoptosisbladder cancercell cycleENO1β-catenin

Identifiers

PMID31431517
PMCPMC6734116
OpenAlexW2969720006

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.