Evidence map›Paper›PMID 27662840›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

NTRK2 is an oncogene and associated with microRNA-22 regulation in human gastric cancer cell lines.

Jinhuai Hu, Yong Huang, Yuanhua Wu, Fengjun Liu, Dong Sun, Kexin Wang, Hui Qu

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 15 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

7 authors at 2 institutions in 1 country.

Jinhuai HuClinical laboratory, Linyi People's Hospital, Linyi, 276003, China.
Yong HuangThe first Department of general surgery, Lanling People's Hospital, Linyi, 277700, China.
Yuanhua WuThe first Department of general surgery, Lanling People's Hospital, Linyi, 277700, China.
Fengjun LiuDepartment of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, JiNan, 250012, China. liufengtt1@aol.com.
Dong SunDepartment of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, JiNan, 250012, China.
Kexin WangDepartment of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, JiNan, 250012, China.
Hui QuDepartment of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, JiNan, 250012, China.
Qilu Hospital of Shandong University · CNLinyi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we examined the roles of neurotrophic tyrosine kinase receptor type 2 (NTRK2) gene in regulating in vitro proliferation and invasion in human gastric cancer. Gene expression of NTRK2 was compared between non-carcinoma gastric epithelial cells and gastric cancer (GC) cells by quantitative RT-PCR (qRT-PCR). NTRK2 was either downregulated or upregulated in MKN-28 and SNU-719 cells. The effect of NTRK2 downregulation or upregulation on GC in vitro development was analyzed by qRT-PCR, western blot, proliferation assay, and invasion assay, respectively. The upstream regulator of NTRK2, microRNA-22 (miR-22), was evaluated by dual-luciferase assay. MiR-22 was then upregulated in MKN-28 and SNU-719 cells to examine its regulation on NTRK2 and its encoded protein, tyrosine kinase receptor B (TrkB). In miR-22-upregulated MKN-28 and SNU-719 cells, NTRK2 was further overexpressed to evaluate functional interaction between miR-22 and NTRK2 in GC. NTRK2 was aberrantly upregulated in GC cell lines than in normal gastric cells. In MKN-28 and SNU-719 cells, NTRK2 downregulation inhibited whereas NTRK2 upregulation promoted GC proliferation and invasion in vitro. MiR-22 was verified to be an inverse upstream regulator of NTRK2. In miR-22-upregulated MKN-28 and SNU-719 cells, NTRK2 overexpression partially reversed the miR-22-induced inhibition on cancer proliferation and invasion. NTRK2 is an oncogene and reversely associated with miR-22 in regulating in vitro cancer development in GC.

Indexed as

Cell MovementCell ProliferationGene Expression Regulation, NeoplasticApoptosisBlotting, WesternDown-RegulationHumansMembrane GlycoproteinsMicroRNAsNeoplasm InvasivenessOncogenesProtein-Tyrosine KinasesReal-Time Polymerase Chain ReactionReceptor, trkBReverse Transcriptase Polymerase Chain ReactionRNA, MessengerMembrane GlycoproteinsMicroRNAsMIRN22 microRNA, humanProtein-Tyrosine KinasesReceptor, trkBRNA, Messengertropomyosin-related kinase-B, humanGastric cancerMigrationmiR-22NTRK2ProliferationTrkB

Identifiers

PMID27662840
OpenAlexW2521338769

What OpenQuestion holds

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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.