Evidence map›Paper›PMID 19688824›Full record

ArticleInternational journal of cancer2010

Phosphoglycerate kinase 1 a promoting enzyme for peritoneal dissemination in gastric cancer.

Derek Zieker, Ingmar Königsrainer, Isabel Tritschler, Markus Löffler, Stefan Beckert, Frank Traub, Kay Nieselt, Sarah Bühler, Michael Weller, Jochen Gaedcke and 4 more

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

71 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
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  6. The regulatory roles and clinical significance of glycolysis in tumor.Cancer communications (London, England) · 2024
    Review
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11 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 2 countries.

Derek ZiekerDepartment of General Visceral, Transplant Surgery Comprehensive Cancer Center, University of Tuebingen, D-72076 Tuebingen, Germany. derek.zieker@med.uni-tuebingen.de
Ingmar Königsrainer
Isabel Tritschler
Markus Löffler
Stefan Beckert
Frank Traub
Kay Nieselt
Sarah Bühler
Michael Weller
Jochen Gaedcke
Russell S Taichman
Hinnak Northoff
Björn L D M Brücher
Alfred Königsrainer
University of Tübingen · DEHertie Institute for Clinical Brain Research · DEUniversity of Göttingen · DEUniversity of Michigan–Ann Arbor · USZero to Three · US

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J. · 2004 to 2024
$29.6M
NCI NIH HHS CA93900NCI NIH HHS P01 CA093900
6 · The paper itself

Abstract

Peritoneal carcinomatosis is a frequent finding in gastric cancer associated with a poor prognosis. The features that enable gastric tumors to disseminate are poorly understood until now. Previously, we showed elevated mRNA levels of phosphoglycerate kinase 1 (PGK1), an adenosine triphosphate-generating enzyme in the glycolytic pathway, the chemokine receptor 4 (CXCR4), the corresponding chemokine ligand 12 (CXCL12) and beta-catenin in specimens from gastric cancer patients with peritoneal carcinomatosis. In this study, the influence of PGK1 on CXCR4 and beta-catenin was assessed as well as the invasiveness of PGK1 overexpressing cancer cells. In this current study, we found that PGK1 regulates the expression of CXCR4 and beta-catenin at the mRNA and protein levels. On the other hand, CXCR4 regulates the expression of PGK1. Plasmid-mediated overexpression of PGK1 dramatically increased the invasiveness of gastric cancer cells. Interestingly, inhibition of CXCR4 in cells overexpressing PGK1 produced only a moderate reduction of invasiveness suggesting that, PGK1 itself has a critical role in tumor invasiveness. Immunohistochemistry in specimens from diffuse gastric cancer patients also revealed an overexpression of PGK1 in patients with development of peritoneal carcinomatosis. Therefore, PGK1 may be a crucial enzyme in peritoneal dissemination. Together these findings suggest that the enhanced expression of PGK1 and its signaling targets CXCR4 and beta-catenin in gastric cancer cells promote peritoneal carcinomatosis. Thus, PGK1 may serve as prognostic marker and/or be a potential therapeutic target to prevent dissemination of gastric carcinoma cells into the peritoneum.

Indexed as

Gene Expression Regulation, Neoplasticbeta CateninBlotting, WesternCell Line, TumorCell MovementCell SurvivalHumansImmunohistochemistryModels, BiologicalPeritoneal NeoplasmsPhosphoglycerate KinaseReceptors, CXCR4Reverse Transcriptase Polymerase Chain ReactionRNA InterferenceSignal TransductionStomach Neoplasmsbeta CateninCTNNB1 protein, humanCXCR4 protein, humanPhosphoglycerate KinaseReceptors, CXCR4

Identifiers

PMID19688824
PMCPMC2811232
OpenAlexW2147577084

What OpenQuestion holds

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Registered trials

None linked

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.