Format

Send to

Choose Destination
Nat Commun. 2010 Jul 13;1:34. doi: 10.1038/ncomms1033.

Identification of high-quality cancer prognostic markers and metastasis network modules.

Author information

1
Computational Chemistry and Bioinformatics Group, Biotechnology Research Institute, National Research Council Canada, Montreal, Quebec, Canada.

Erratum in

  • Nat Commun. 2012;3. doi:10.1038/ncomms1033.

Abstract

Cancer patients are often overtreated because of a failure to identify low-risk cancer patients. Thus far, no algorithm has been able to successfully generate cancer prognostic gene signatures with high accuracy and robustness in order to identify these patients. In this paper, we developed an algorithm that identifies prognostic markers using tumour gene microarrays focusing on metastasis-driving gene expression signals. Application of the algorithm to breast cancer samples identified prognostic gene signature sets for both estrogen receptor (ER) negative (-) and positive (+) subtypes. A combinatorial use of the signatures allowed the stratification of patients into low-, intermediate- and high-risk groups in both the training set and in eight independent testing sets containing 1,375 samples. The predictive accuracy for the low-risk group reached 87-100%. Integrative network analysis identified modules in which each module contained the genes of a signature and their direct interacting partners that are cancer driver-mutating genes. These modules are recurrent in many breast tumours and contribute to metastasis.

PMID:
20975711
PMCID:
PMC2972666
DOI:
10.1038/ncomms1033
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Nature Publishing Group Icon for PubMed Central
Loading ...
Support Center