Evidence map›Paper›PMID 27801851›Full record

ArticleInternational journal of molecular sciences2016

PPIC, EMP3 and CHI3L1 Are Novel Prognostic Markers for High Grade Glioma.

Yuan-Feng Gao, Tao Zhu, Chen-Xue Mao, Zhi-Xiong Liu, Zhi-Bin Wang, Xiao-Yuan Mao, Ling Li, Ji-Ye Yin, Hong-Hao Zhou, Zhao-Qian Liu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  5. Article
  6. Article
  7. Hypoxia-related THBDJournal of cellular and molecular medicine · 2024
    Article
  8. Review
  9. EMP3: A promising biomarker for tumor prognosis and targeted cancer therapy.Cancer biomarkers : section A of Disease markers · 2024
    Review
  10. Article
  11. Article
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  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. EMP3 mediates glioblastoma-associated macrophage infiltration to drive T cell exclusion.Journal of experimental & clinical cancer research : CR · 2021
    Article
  20. 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

10 authors.

Yuan-Feng GaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. gaoyuanfeng126@126.com.
Tao ZhuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. euzhutao@hotmail.com.
Chen-Xue MaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. sharemix@163.com.
Zhi-Xiong LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, China. zhixiongliu@csu.edu.cn.
Zhi-Bin WangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. wangzhibinwalking@163.com.
Xiao-Yuan MaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. xiaoyuanm@csu.edu.cn.
Ling LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. yx132liling@126.com.
Ji-Ye YinDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. yinjiye@csu.edu.cn.
Hong-Hao ZhouDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. HHzhou2003@163.com.
Zhao-Qian LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China. liuzhaoqian63@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current treatment methods for patients diagnosed with gliomas have shown limited success. This is partly due to the lack of prognostic genes available to accurately predict disease outcomes. The aim of this study was to investigate novel prognostic genes based on the molecular profile of tumor samples and their correlation with clinical parameters. In the current study, microarray data (GSE4412 and GSE7696) downloaded from Gene Expression Omnibus were used to identify differentially expressed prognostic genes (DEPGs) by significant analysis of microarray (SAM) between long-term survivors (>2 years) and short-term survivors (≤2 years). DEPGs generated from these two datasets were intersected to obtain a list of common DEPGs. The expression of a subset of common DEPGs was then independently validated by real-time reverse transcription quantitative PCR (qPCR). Survival value of the common DEPGs was validated using known survival data from the GSE4412 and TCGA dataset. After intersecting DEPGs generated from the above two datasets, three genes were identified which may potentially be used to determine glioma patient prognosis. Independent validation with glioma patients tissue (

Indexed as

AdultAgedAge FactorsBiomarkers, TumorChitinase-3-Like Protein 1Cyclophilin CDacarbazineFemaleGene Expression Regulation, NeoplasticGliomaHumansKaplan-Meier EstimateMaleMembrane GlycoproteinsMicroarray AnalysisMiddle AgedBiomarkers, TumorCHI3L1 protein, humanChitinase-3-Like Protein 1Cyclophilin CDacarbazineEMP3 protein, humanMembrane GlycoproteinsTemozolomideCHI3L1DEPGsEMP3novel glioma markersPPIC

Identifiers

PMID27801851
PMCPMC5133809

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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.