A validated gene expression profile for detecting clinical outcome in breast cancer using artificial neural networks

被引:0
|
作者
L. J. Lancashire
D. G. Powe
J. S. Reis-Filho
E. Rakha
C. Lemetre
B. Weigelt
T. M. Abdel-Fatah
A. R. Green
R. Mukta
R. Blamey
E. C. Paish
R. C. Rees
I. O. Ellis
G. R. Ball
机构
[1] University of Manchester,Clinical and Experimental Pharmacology, Paterson Institute for Cancer Research
[2] Nottingham Trent University,John Van Geest Cancer Research Centre
[3] Nottingham University Hospitals Trust and University of Nottingham,Department of Histopathology
[4] The Breakthrough Breast Cancer Research Centre,undefined
[5] Institute of Cancer Research,undefined
[6] Chester Beatty Laboratories,undefined
[7] Department of Surgery,undefined
[8] Breast Institute,undefined
[9] City Hospital Nottingham,undefined
[10] Signal Transduction Laboratory,undefined
[11] London Research Institute,undefined
[12] Lincoln’s Inn Fields Laboratories,undefined
来源
Breast Cancer Research and Treatment | 2010年 / 120卷
关键词
Breast cancer; Prognosis; Bioinformatics; Survival; Hypoxia; Biomarkers;
D O I
暂无
中图分类号
学科分类号
摘要
Gene expression microarrays allow for the high throughput analysis of huge numbers of gene transcripts and this technology has been widely applied to the molecular and biological classification of cancer patients and in predicting clinical outcome. A potential handicap of such data intensive molecular technologies is the translation to clinical application in routine practice. In using an artificial neural network bioinformatic approach, we have reduced a 70 gene signature to just 9 genes capable of accurately predicting distant metastases in the original dataset. Upon validation in a follow-up cohort, this signature was an independent predictor of metastases free and overall survival in the presence of the 70 gene signature and other factors. Interestingly, the ANN signature and CA9 expression also split the groups defined by the 70 gene signature into prognostically distinct groups. Subsequently, the presence of protein for the principal prognosticator gene was categorically assessed in breast cancer tissue of an experimental and independent validation patient cohort, using immunohistochemistry. Importantly our principal prognosticator, CA9, showed that it is capable of selecting an aggressive subgroup of patients who are known to have poor prognosis.
引用
收藏
页码:83 / 93
页数:10
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