Evidence map›Paper›PMID 29049217›Full record

ArticleMedicine2017

Identification of novel therapeutic target genes and pathway in pancreatic cancer by integrative analysis.

Bangli Hu, Cheng Shi, Hai-Xing Jiang, Shan-Yu Qin

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  6. The emerging role of the KCTD proteins in cancer.Cell communication and signaling : CCS · 2021
    Review
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  15. Overexpression of Kin of IRRE-Like Protein 1 (KIRREL) in Gastric Cancer and Its Clinical Prognostic Significance.Medical science monitor : international medical journal of experimental and clinical research · 2018
    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

4 authors at 1 institution in 1 country.

Bangli HuDepartment of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Cheng Shi
Hai-Xing Jiang
Shan-Yu Qin
First Affiliated Hospital of GuangXi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene alterations are crucial to the molecular pathogenesis of pancreatic cancer. The present study was designed to identify the potential candidate genes in the pancreatic carcinogenesis.

methodsGene Expression Omnibus database (GEO) datasets of pancreatic cancer tissue were retrieval and the differentially expressed genes (DEGs) from individual microarray data were merged. Gene Ontology (GO) enrichment analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, protein-protein interaction (PPI) networks, and gene coexpression analysis were performed.

resultsThree GEO datasets, including 74 pancreatic cancer samples and 55 controls samples were selected. A total of 2325 DEGs were identified, including 1383 upregulated and 942 downregulated genes. The GO terms for molecular functions, biological processes, and cellular component were protein binding, small molecule metabolic process, and integral to membrane, respectively. The most significant pathway in KEGG analysis was metabolic pathways. PPI network analysis indicated that the significant hub genes including cytochrome P450, family 2, subfamily E, polypeptide 1 (CYP2E1), mitogen-activated protein kinase 3 (MAPK3), and phospholipase C, gamma 1 (PLCG1). Gene coexpression network analysis identified 4 major modules, and the potassium channel tetramerization domain containing 10 (KCTD10), kin of IRRE like (KIRREL), dipeptidyl-peptidase 10 (DPP10), and unc-80 homolog (UNC80) were the hub gene of each modules, respectively.

conclusionOur integrative analysis provides a comprehensive view of gene expression patterns associated with the pancreatic carcinogenesis.

Indexed as

CarcinogenesisCarrier ProteinsCase-Control StudiesCytochrome P-450 CYP2E1Databases, GeneticDipeptidyl-Peptidases and Tripeptidyl-PeptidasesGene Expression ProfilingGene Expression Regulation, NeoplasticGene OntologyHumansMembrane ProteinsMitogen-Activated Protein Kinase 3Pancreatic NeoplasmsPhospholipase C gammaPotassium Channels, Voltage-GatedProtein Interaction MapsCarrier ProteinsCytochrome P-450 CYP2E1Dipeptidyl-Peptidases and Tripeptidyl-PeptidasesDPP10 protein, humanKCTD10 protein, humanKIRREL1 protein, humanMembrane ProteinsMitogen-Activated Protein Kinase 3Phospholipase C gammaPLCG1 protein, humanPotassium Channels, Voltage-GatedUnc80 protein, human

Identifiers

PMID29049217
PMCPMC5662383
OpenAlexW2765762897

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

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.