Evidence map›Paper›PMID 26834490›Full record

ArticleOncoTargets and therapy2016

Expression of MECOM is associated with unfavorable prognosis in glioblastoma multiforme.

Aiwu Hou, Lizhen Zhao, Fuzhen Zhao, Weiliang Wang, Jianyi Niu, Bingxuan Li, Zhongjin Zhou, Dongyuan Zhu

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. International journal of molecular sciences · 2022
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Prognostic Significance of Zinc Finger E-Box-Binding Homeobox Family in Glioblastoma.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  13. Prognostic Significance of TNFR-Associated Factor 1 and 2 (TRAF1 and TRAF2) in Glioblastoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  14. Article
  15. Article
  16. Article
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 4 institutions in 1 country.

Aiwu HouDepartment of Neurology, Yidu Central Hospital of Weifang City.
Lizhen ZhaoDepartment of Neurology, Yidu Central Hospital of Weifang City.
Fuzhen ZhaoDepartment of Orthopedics, People's Hospital of Qingzhou City.
Weiliang WangDepartment of Psychiatrics, People's Third Hospital of Weifang City, Weifang.
Jianyi NiuDepartment of Neurology, Yidu Central Hospital of Weifang City.
Bingxuan LiDepartment of Neurology, Yidu Central Hospital of Weifang City.
Zhongjin ZhouDepartment of Neurology, Yidu Central Hospital of Weifang City.
Dongyuan ZhuDepartment of Medical Oncology, Shandong Cancer Hospital and Institute, Shandong Academy of Medical Sciences.
Yidu Central Hospital of Weifang · CNQingzhou City People's Hospital · CNShandong First Medical University · CNWeifang People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMDS1 and EVI1 complex locus protein EVI1 (MECOM) is an oncogenic transcription factor in several kinds of cancers. However, the clinical significance of MECOM in glioblastoma multiforme (GBM) has not been well elucidated. PATIENTS AND

methodsOur study enrolled 86 resected samples of GBM in three medical centers. We detected the expression of MECOM in all the 86 samples by immunohistochemistry and compared the difference of MECOM mRNA between tumor tissues and adjacent tissues with real-time polymerase chain reaction. With immunoblotting, we detected the MECOM expression in different GBM cell lines. Moreover, we analyzed the correlation between MECOM expression and clinicopathologic factors with chi-square test, and evaluated the prognostic value of MECOM with univariate and multivariate analysis.

resultsIn GBM tissue, the percentage of MECOM high expression is 41.9% (36/86). The mRNA of MECOM in tumor tissues is remarkably higher than that in adjacent tissues, indicating the oncogenic role of MECOM in GBM. MECOM exists in all the detected cell lines with different abundance. Moreover, MECOM is correlated with poorer overall survival rate (P=0.033) and can be identified as an independent prognostic factor in GBM (P=0.042).

conclusionMECOM could be considered as an independent prognostic factor in GBM, predicting it as a potential and promising molecular drug target.

Indexed as

glioblastoma multiformeMECOMprognosisprogression

Identifiers

PMID26834490
PMCPMC4716764
OpenAlexW2233483251

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.