Evidence map›Paper›PMID 20087356›Full record

SynthesisBritish journal of cancer2010

Large meta-analysis of multiple cancers reveals a common, compact and highly prognostic hypoxia metagene.

F M Buffa, A L Harris, C M West, C J Miller

Erratum issuedOpen access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in British journal of cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 341 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
341citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 4% 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

341 citing papers in PubMed, 2 syntheses or guidelines pooled it, 593 citations in OpenAlex.

  1. Pooled it
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  5. DRP1 depletion protects NK cells from hypoxia-induced dysfunction.Redox report : communications in free radical research · 2026
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  17. Multi-omics exploration of hypoxia in gastric cancer.World journal of surgical oncology · 2026
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281 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

F M BuffaWeatherall Institute of Molecular Medicine, University of Oxford, Oxford, OX3 9DS, UK. francesca.buffa@imm.ox.ac.uk
A L Harris
C M West
C J Miller
MRC Weatherall Institute of Molecular Medicine · GBUniversity of Manchester · GB

Funding

Cancer Research UKMedical Research Council
6 · The paper itself

Abstract

backgroundThere is a need to develop robust and clinically applicable gene expression signatures. Hypoxia is a key factor promoting solid tumour progression and resistance to therapy; a hypoxia signature has the potential to be not only prognostic but also to predict benefit from particular interventions.

methodsAn approach for deriving signatures that combine knowledge of gene function and analysis of in vivo co-expression patterns was used to define a common hypoxia signature from three head and neck and five breast cancer studies. Previously validated hypoxia-regulated genes (seeds) were used to generate hypoxia co-expression cancer networks.

resultsA common hypoxia signature, or metagene, was derived by selecting genes that were consistently co-expressed with the hypoxia seeds in multiple cancers. This was highly enriched for hypoxia-regulated pathways, and prognostic in multivariate analyses. Genes with the highest connectivity were also the most prognostic, and a reduced metagene consisting of a small number of top-ranked genes, including VEGFA, SLC2A1 and PGAM1, outperformed both a larger signature and reported signatures in independent data sets of head and neck, breast and lung cancers.

conclusionCombined knowledge of multiple genes' function from in vitro experiments together with meta-analysis of multiple cancers can deliver compact and robust signatures suitable for clinical application.

Indexed as

HypoxiaBreast NeoplasmsGene ExpressionGene Expression RegulationHead and Neck NeoplasmsHumansMetagenomeModels, BiologicalPrognosis

Identifiers

PMID20087356
PMCPMC2816644
OpenAlexW2084116712

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.