A Signature Inferred from Drosophila Mitotic Genes Predicts Survival of Breast Cancer Patients
Author(s) -
Christian Damasco,
Antonio Lembo,
Maria Patrizia Somma,
Maurizio Gatti,
Ferdinando Di Cunto,
Paolo Provero
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0014737
Subject(s) - gene signature , breast cancer , biology , gene , gene expression profiling , cytokinesis , microarray , dna microarray , cancer , microarray analysis techniques , mitosis , computational biology , bioinformatics , gene expression , genetics , cancer research , cell division , cell
The classification of breast cancer patients into risk groups provides a powerful tool for the identification of patients who will benefit from aggressive systemic therapy. The analysis of microarray data has generated several gene expression signatures that improve diagnosis and allow risk assessment. There is also evidence that cell proliferation-related genes have a high predictive power within these signatures. Methods We thus constructed a gene expression signature (the DM signature) using the human orthologues of 108 Drosophila melanogaster genes required for either the maintenance of chromosome integrity (36 genes) or mitotic division (72 genes). Results The DM signature has minimal overlap with the extant signatures and is highly predictive of survival in 5 large breast cancer datasets. In addition, we show that the DM signature outperforms many widely used breast cancer signatures in predictive power, and performs comparably to other proliferation-based signatures. For most genes of the DM signature, an increased expression is negatively correlated with patient survival. The genes that provide the highest contribution to the predictive power of the DM signature are those involved in cytokinesis. Conclusion This finding highlights cytokinesis as an important marker in breast cancer prognosis and as a possible target for antimitotic therapies.
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