Prognosis of stage II colon cancer by non-neoplastic mucosa gene expression profiling

被引:41
作者
Barrier, A.
Roser, F.
Boelle, P-Y
Franc, B.
Tse, C.
Brault, D.
Lacaine, F.
Houry, S.
Callard, P.
Penna, C.
Debuire, B.
Flahault, A.
Dudoit, S.
Lemoine, A.
机构
[1] Hop Paul Brousse, AP HP, Serv Biochim, F-94804 Villejuif, France
[2] Hop Tenon, AP HP, Serv Chirurg Digest, F-75970 Paris, France
[3] INSERM, UMR S707, Paris, France
[4] Univ Paris 06, Fac Med, F-75252 Paris 05, France
[5] Univ Calif Berkeley, Sch Publ Hlth, Div Biostat, Berkeley, CA 94720 USA
[6] INSERM, UMR S602, Villejuif, France
[7] Univ Paris 11, Fac Med, Villejuif, France
[8] Hop Ambroise Pare, AP HP, Serv Anat Pathol, Boulogne, France
[9] Univ Versailles, Fac Med, Boulogne, France
[10] Hop Tenon, AP HP, Serv Biochim, F-75970 Paris, France
[11] Hop Tenon, AP HP, Serv Anat Pathol, F-75970 Paris, France
[12] Hop Ambroise Pare, AP HP, Serv Chirurg Digest, Boulogne, France
关键词
functional genomics; colon cancer; prognosis prediction; non neoplastic mucosa; cross validation; cDNA arrays;
D O I
10.1038/sj.onc.1210060
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
We have assessed the possibility to build a prognosis predictor (PP), based on non-neoplastic mucosa microarray gene expression measures, for stage II colon cancer patients. Non-neoplastic colonic mucosa mRNA samples from 24 patients (10 with a metachronous metastasis, 14 with no recurrence) were pro. led using the Affymetrix HGU133A GeneChip. Patients were repeatedly and randomly divided into 1000 training sets (TSs) of size 16 and validation sets (VS) of size 8. For each TS/VS split, a 70-gene PP, identified on the TS by selecting the 70 most differentially expressed genes and applying diagonal linear discriminant analysis, was used to predict the prognoses of VS patients. Mean prognosis prediction performances of the 70-gene PP were 81.8% for accuracy, 73.0% for sensitivity and 87.1% for specific city. Informative genes suggested branching signal-transduction pathways with possible extensive networks between individual pathways. They also included genes coding for proteins involved in immune surveillance. In conclusion, our study suggests that one can build an accurate PP for stage II colon cancer patients, based on non-neoplastic mucosa microarray gene expression measures.
引用
收藏
页码:2642 / 2648
页数:7
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