Evidence map›Paper›PMID 25590580›Full record

ArticleCell cycle (Georgetown, Tex.)2015

Frequent amplification of PTP1B is associated with poor survival of gastric cancer patients.

Na Wang, Junjun She, Wei Liu, Jing Shi, Qi Yang, Bingyin Shi, Peng Hou

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  5. MultiscaleJournal of chemical information and modeling · 2024
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  11. Isothiocyanate FromFrontiers in cell and developmental biology · 2021
    Article
  12. Review
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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 1 institution in 1 country.

Na Wanga Department of Endocrinology ; The First Affiliated Hospital of Xi'an Jiaotong University School of Medicine ; Xi'an , People's Republic of China.
Junjun She
Wei Liu
Jing Shi
Qi Yang
Bingyin Shi
Peng Hou
First Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein tyrosine phosphatase 1B (PTP1B), a non-transmembrane protein tyrosine phosphatase, has been implicated in gastric pathogenesis. Several lines of recent evidences have shown that PTP1B is highly amplified in breast and prostate cancers. The aim of this study was to investigate PTP1B amplification in gastric cancer and its association with poor prognosis of gastric cancer patients, and further determine the role of PTP1B in gastric tumorigenesis. Our data demonstrated that PTP1B was significantly up-regulated in gastric cancer tissues as compared with matched normal gastric tissues by using quantitative RT-PCR (qRT-PCR) assay. In addition, copy number analysis showed that PTP1B was amplified in 68/131 (51.9%) gastric cancer cases, whereas no amplification was found in the control subjects. Notably, PTP1B amplification was positively associated with its protein expression, and was significantly related to poor survival of gastric cancer patients. Knocking down PTP1B expression in gastric cancer cells significantly inhibited cell proliferation, colony formation, migration and invasion, and induced cell cycle arrested and apoptosis. Mechanically, PTP1B promotes gastric cancer cell proliferation, survival and invasiveness through modulating Src-related signaling pathways, such as Src/Ras/MAPK and Src/phosphatidylinositol-3-kinase (PI3K)/Akt pathways. Collectively, our data demonstrated frequent overexpression and amplification PTP1B in gastric cancer, and further determined the oncogenic role of PTP1B in gastric carcinogenesis. Importantly, PTP1B amplification predicts poor survival of gastric cancer patients.

Indexed as

Gene AmplificationAgedApoptosisCell Cycle CheckpointsCell DifferentiationCell Line, TumorCell MovementCell ProliferationDown-RegulationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansKaplan-Meier EstimateLymphatic MetastasisProtein Tyrosine Phosphatase, Non-Receptor Type 1PTPN1 protein, humanRNA, MessengerAkt, serine/threonine protein kinaseDMEM, Dulbecco's modified Eagles mediumDMSO, dimethyl sulfoxideEDTA, Ethylenediaminetetraacetic acidEMT, epithelial-to-mesenchymal transitionErk, elk-related tyrosine kinaseFAK, focal adhesion kinaseFITC, fluoresceine isothiocyanateFOXO3a, Forkhead class O transcription factor 3aGastric cancergenomic amplificationH&E, hematoxylin and eosinHR, hazard ratioHRP, horseradish peroxidaseIHC, immunohistochemistryMAPK, mitogen-activated protein kinaseMdm2, mouse double minute 2MMPs, metalloproteinasesMTT, 3-[4, 5-dimethylthiazol-2-yl]-2, 5-diphenyl tetrazolium bromidePBS, phosphate buffered salinePI3K, phosphatidylinositol 3-kinasepoor prognosisPTP1BPTP1B, protein tyrosine phosphatase 1BPVDF, polyvinylidene fluorideRPMI 1640, Roswell Park Memorial Institute 1640RT-PCR, Reverse-transcription polymerase chain reactionSDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrophoresissignaling pathwayssiRNA, short interfering RNA.

Identifiers

PMID25590580
PMCPMC4418292
OpenAlexW1807129303

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.