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Cited by 556

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

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

Open access
Buffa, F M, Harris, A L, West, C M, Miller, C J·2010·British Journal of Cancer

Abstract

BACKGROUND: There 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. METHODS: An 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. RESULTS: A 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. CONCLUSION: Combined 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.

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Crossref · 10.1038/sj.bjc.6605450

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Metadata

Authors
Buffa, F. M., Harris, A. L., West, C. M., & Miller, C. J.
Venue
British Journal of Cancer
Published
2010-01-19
Volume
102
Issue
2
Pages
428-435
ISSN
  • 0007-0920 (ISSN-L)
  • 1532-1827
OpenAlex
W2084116712
Cited by
556
References
7
FWCI
0.87
Type
journal article
Language
en
Open access
hybrid

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