Evidence map›Paper›PMID 27314162›Full record

ArticleCancer biology & therapy2016

Overexpressed targeting protein for Xklp2 (TPX2) serves as a promising prognostic marker and therapeutic target for gastric cancer.

Bo Liang, Wenjuan Zheng, Lu Fang, Linquan Wu, Fan Zhou, Xiangbao Yin, Xin Yu, Zhenhong Zou

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
4.2field-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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  13. TPX2 Promotes Metastasis and Serves as a Marker of Poor Prognosis in Non-Small Cell Lung Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  14. Article
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  16. CDK5-mediated phosphorylation and stabilization of TPX2 promotes hepatocellular tumorigenesis.Journal of experimental & clinical cancer research : CR · 2019
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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

8 authors at 3 institutions in 1 country.

Bo Lianga Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Wenjuan Zhengb Jiangxi Provincial Center for Disease Control and Prevention , Nanchang , Jiangxi , China.
Lu Fanga Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Linquan Wua Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Fan Zhoua Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Xiangbao Yina Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Xin Yua Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Zhenhong Zoua Department of General Surgery , The Second Affiliated Hospital of Nanchang University , Nanchang , Jiangxi , China.
Second Affiliated Hospital of Nanchang University · CNNanchang University · CNNanchang Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The targeting protein for Xenopus kinesin-like protein 2 (TPX2) is a putative oncogene in different human cancers. This study assessed TPX2 expression in gastric cancer tissue samples and then determined the effects of TPX2 knockdown on the regulation of gastric cancer cell malignant behaviors in vitro. Tissue samples from 115 gastric cancer patients were analyzed for TPX2 expression. The effects of TPX2 siRNA on gastric cancer cells were assessed in vitro, including cell viability, cell cycle distribution, apoptosis, migration, and invasion. The data showed that TPX2 was overexpressed in gastric cancer tissues compared to that in the adjacent normal epithelia. Moreover, TPX2 overexpression was associated with a poor overall survival and was an independent prognostic predictor of gastric cancer. In addition, the in vitro study further confirmed the ex vivo data, i.e., knockdown of TPX2 expression reduced gastric cancer cell viability but induced apoptosis and arrested cells at the G2/M phase of the cell cycle. Knockdown of TPX2 expression also inhibited the tumor cell migration and invasion capacity in vitro. At the gene level, knockdown of TPX2 expression upregulated the levels of cyclin B1, cdk4, p53, Bax, caspase-3, and E-cadherin, but downregulated the levels of cyclin D1, cdk2, N-cadherin, slug, matrix metalloprotease (MMP)-2, and MMP-9, suggesting that knockdown of TPX2 expression suppressed tumor cell epithelial-mesenchymal transition (EMT). This study demonstrated that detection of TPX2 overexpression could serve as a prognostic marker and therapeutic target for gastric cancer.

Indexed as

ApoptosisBiomarkers, TumorCell Cycle ProteinsCell Growth ProcessesCell Line, TumorEpithelial-Mesenchymal TransitionGene Expression ProfilingGene Knockdown TechniquesHumansMicrotubule-Associated ProteinsNuclear ProteinsPrognosisStomach NeoplasmsTransfectionBiomarkers, TumorCell Cycle ProteinsMicrotubule-Associated ProteinsNuclear ProteinsTPX2 protein, humanApoptosiscell cycle arrestdrug targetEMTgastric cancerprognostic markerTPX2

Identifiers

PMID27314162
PMCPMC5004702
OpenAlexW2435937640

What OpenQuestion holds

Textmetadata
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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.