Evidence map›Paper›PMID 23686313›Full record

ArticleOncogene2014

PPISURV: a novel bioinformatics tool for uncovering the hidden role of specific genes in cancer survival outcome.

A V Antonov, M Krestyaninova, R A Knight, I Rodchenkov, G Melino, N A Barlev

Abstract read
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In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

45 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  15. Inhibition ofMolecular cancer therapeutics · 2018
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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

6 authors.

A V Antonov1] Toxicology Unit, Hodgkin Building, Medical Research Council, Leicester University, Leicester, UK [2] Molecular Pharmacology Laboratory, Technological University, St-Petersburg, Russia.
M KrestyaninovaInstitute for Molecular Medicine Finland FIMM, University of Helsinki; Helsinki, Finland.
R A KnightToxicology Unit, Hodgkin Building, Medical Research Council, Leicester University, Leicester, UK.
I RodchenkovDonnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, ON, Canada.
G Melino1] Toxicology Unit, Hodgkin Building, Medical Research Council, Leicester University, Leicester, UK [2] Molecular Pharmacology Laboratory, Technological University, St-Petersburg, Russia [3] Department of Experimental Medicine and Surgery, University of Rome 'Tor Vergata', Via Montpellier 1, Rome, Italy.
N A Barlev1] Molecular Pharmacology Laboratory, Technological University, St-Petersburg, Russia [2] Department of Biochemistry, University of Leicester, Leicester, UK [3] Gene Expression Programme, Institute of Cytology, St-Petersburg, Russia.

Funding

Medical Research Council MC_U132670600
6 · The paper itself

Abstract

Multiple clinical studies have correlated gene expression with survival outcome in cancer on a genome-wide scale. However, in many cases, no obvious correlation between expression of well-known tumour-related genes (that is, p53, p73 and p21) and survival rates of patients has been observed. This can be mainly explained by the complex molecular mechanisms involved in cancer, which mask the clinical relevance of a gene with multiple functions if only gene expression status is considered. As we demonstrate here, in many such cases, the expression of the gene interaction partners (gene 'interactome') correlates significantly with cancer survival and is indicative of the role of that gene in cancer. On the basis of this principle, we have implemented a free online datamining tool (http://www.bioprofiling.de/PPISURV). PPISURV automatically correlates expression of an input gene interactome with survival rates on >40 publicly available clinical expression data sets covering various tumours involving about 8000 patients in total. To derive the query gene interactome, PPISURV employs several public databases including protein-protein interactions, regulatory and signalling pathways and protein post-translational modifications.

Indexed as

Computational BiologyCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsGene Expression ProfilingGenes, p53HumansNeoplasmsNuclear ProteinsSurvival RateTreatment OutcomeTumor Protein p73Tumor Suppressor ProteinsCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsNuclear ProteinsTP73 protein, humanTumor Protein p73Tumor Suppressor Proteins

Identifiers

PMID23686313

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.