Colon cancer prognosis prediction by gene expression profiling

被引:78
作者
Barrier, A [1 ]
Lemoine, A
Boelle, PY
Tse, C
Brault, D
Chiappini, F
Breittschneider, J
Lacaine, F
Houry, S
Huguier, M
Van der Laan, MJ
Speed, T
Debuire, B
Flahault, A
Dudoit, S
机构
[1] Univ Paris 06, Hop Tenon, Serv Chirurg Digest, Assistance Publ, F-75020 Paris, France
[2] Univ Paris 06, Fac Med St Antoine, INSERM U444, F-75571 Paris, France
[3] Univ Calif Berkeley, Sch Publ Hlth, Div Biostat, Berkeley, CA 94720 USA
[4] Univ Paris 11, Hop Paul Brousse, Serv Biochem, INSERM U602, F-94800 Villejuif, France
[5] Univ Paris 06, Hop Tenon, Serv Biochem, Assistance Publ, F-75020 Paris, France
[6] Univ Calif Berkeley, Dept Stat, Berkeley, CA 94720 USA
关键词
functional genomics; colon cancer; prognosis prediction; non-neoplastic mucosa; cross-validation;
D O I
10.1038/sj.onc.1208984
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study assessed the possibility to build a prognosis predictor, based on microarray gene expression measures, in stage II and III colon cancer patients. Tumour ( T) and non-neoplastic mucosa ( NM) mRNA samples from 18 patients ( nine with a recurrence, nine with no recurrence) were pro. led using the Affymetrix HGU133A GeneChip. The k-nearest neighbour method was used for prognosis prediction using T and NM gene expression measures. Six-fold cross-validation was applied to select the number of neighbours and the number of informative genes to include in the predictors. Based on this information, one T-based and one NM-based predictor were proposed and their accuracies were estimated by double cross-validation. In six-fold cross-validation, the lowest numbers of informative genes giving the lowest numbers of false predictions ( two out of 18) were 30 and 70 with the T and NM gene expression measures, respectively. A 30-gene T-based predictor and a 70-gene NM-based predictor were then built, with estimated accuracies of 78 and 83%, respectively. This study suggests that one can build an accurate prognosis predictor for stage II and III colon cancer patients, based on gene expression measures, and one can use either tumour or non-neoplastic mucosa for this purpose.
引用
收藏
页码:6155 / 6164
页数:10
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