Evidence map›Paper›PMID 27655637›Full record

ArticleOncotarget2016

COL3A1 and SNAP91: novel glioblastoma markers with diagnostic and prognostic value.

Yuan-Feng Gao, Xiao-Yuan Mao, Tao Zhu, Chen-Xue Mao, Zhi-Xiong Liu, Zhi-Bin Wang, Ling Li, Xi Li, Ji-Ye Yin, Wei Zhang and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 91 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.

Yuan-Feng GaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Xiao-Yuan MaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Tao ZhuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Chen-Xue MaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Zhi-Xiong LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Zhi-Bin WangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Ling LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Xi LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Ji-Ye YinDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Wei ZhangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Hong-Hao ZhouDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Zhao-Qian LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, P. R. China.
Central South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although patients with glioblastoma (GBM) have grave prognosis, significant variability in patient outcome is observed. This study aims to identify novel targets for GBM diagnosis and therapy. Microarray data (GSE4290, GSE7696, and GSE4412) obtained from the Gene Expression Omnibus was used to identify the differentially expressed genes (DEGs) by significant analysis of microarray (SAM). Intersection of the identified DEGs for each profile revealed 46 DEGs in GBM. A subset of common DEGs were validated by real-time reverse transcription quantitative PCR (qPCR). The prognostic value of some of the markers was also studied. We determined that RRM2 and COL3A1 were increased and directly correlated with glioma grade, while SH3GL2 and SNAP91 were decreased in GBM and inversely correlated with glioma grade. Kaplan-Meir analysis of GSE7696 revealed that COL3A1 and SNAP91 correlated with survival, suggesting that COL3A1 and SNAP91 may be suitable biomarkers for diagnostic or therapeutic strategies for GBM.

Indexed as

AdultBiomarkers, TumorBrain NeoplasmsCollagen Type IIIFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene OntologyGlioblastomaHumansKaplan-Meier EstimateMaleMiddle AgedMonomeric Clathrin Assembly ProteinsPrognosisBiomarkers, Tumorclathrin assembly protein AP180COL3A1 protein, humanCollagen Type IIIMonomeric Clathrin Assembly ProteinsCOL3A1glioblastomanovel glioblastoma markersprognostic valueSNAP91

Identifiers

PMID27655637
PMCPMC5342568
OpenAlexW2518752141

What OpenQuestion holds

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LicenceCC BY
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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.