Clinical and Pathophysiological Implications of Chromosomal Alterations in Adrenocortical Tumors: An Integrated Genomic Approach

被引:40
作者
Barreau, Olivia [1 ,8 ,9 ]
de Reynies, Aurelien [10 ]
Wilmot-Roussel, Hortense [1 ,8 ,9 ]
Guillaud-Bataille, Marine [1 ,7 ,9 ]
Auzan, Colette [1 ,9 ]
Rene-Corail, Fernande [1 ,9 ]
Tissier, Frederique [1 ,4 ,8 ,9 ]
Dousset, Bertrand [1 ,5 ,8 ,9 ]
Bertagna, Xavier [1 ,2 ,3 ,6 ,8 ,9 ]
Bertherat, Jerome [1 ,3 ,6 ,8 ,9 ]
Clauser, Eric [7 ]
Assie, Guillaume [1 ,3 ,8 ,9 ]
机构
[1] Inst Cochin, Inst Natl Sante & Rech Med, U1016, F-75014 Paris, France
[2] Rare Adrenal Canc Network COrtico MEdullo Tumeurs, F-75014 Paris, France
[3] Hop Cochin, AP HP, Dept Endocrinol, F-75014 Paris, France
[4] Hop Cochin, Assistance Publ Hop Paris, Dept Pathol, F-75014 Paris, France
[5] Hop Cochin, Assistance Publ Hop Paris, Unit Digest & Endocrine Surg, F-75014 Paris, France
[6] Hop Cochin, Assistance Publ Hop Paris, Ctr Rare Adrenal Dis, F-75014 Paris, France
[7] Hop Cochin, Assistance Publ Hop Paris, Oncogenet Unit, F-75014 Paris, France
[8] Univ Paris 05, F-75006 Paris, France
[9] Ctr Natl Rech Sci, Unite Mixte Rech 8104, F-75014 Paris, France
[10] Ligue Natl Le Canc, Programme Cartes Identite Tumeurs, F-75013 Paris, France
关键词
PROGNOSTIC VALUE; CANCER; CARCINOMA; GENE; MICROARRAY; EXPRESSION; MALIGNANCY; FEATURES; CLASSIFICATION; HYBRIDIZATION;
D O I
10.1210/jc.2011-1588
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Diagnosing malignancy of adrenocortical tumors (ACT) and predicting prognosis in carcinomas are often challenging. Transcriptome markers have recently emerged, providing promising clinical relevance and improved pathophysiological knowledge. Whether tumoral chromosomal alterations provide similar information is not known. The aim was to evaluate the diagnostic and prognostic value of chromosomal alterations in ACT and to identify genes associated with benign and malignant tumorigenesis. Experimental Design: Chromosomal alterations of 86 adenomas and 52 carcinomas were identified by comparative genomic hybridization arrays and/or quantitative PCR. Results: A larger proportion of the genome is altered in carcinomas compared with adenomas (44 vs. 10%, P = 2.10(-10)). In adenomas, the 9q34 region, which includes the steroidogenic factor 1 locus, is commonly gained and associated with an overexpression of steroidogenic factor 1 (SF-1). In carcinomas, recurrent gains include chromosomes 5, 7, 12, 16, 19, and 20 and recurrent losses chromosomes 13 and 22. Filtering the genes from these regions according to their expression profile identified genes potentially relevant to adrenocortical tumorigenesis. A diagnostic tool was built by combining DNA copy number estimates at six loci (5q, 7p, 11p, 13q, 16q, and 22q). This tool discriminates carcinomas from adenomas in an independent validation cohort (sensitivity 100%, specificity 83%). In carcinomas, the number of chromosomal alterations was not associated with survival (Cox P = 0.84). A prognostic tool based on tumor DNA was designed with a clustering strategy and validated in an independent cohort. Conclusions: Chromosomal alterations in ACT discriminate carcinomas from adenomas and contain prognostic information. Chromosomal alterations alter the expression of genes important for tumorigenesis. (J Clin Endocrinol Metab 97: E301-E311, 2012)
引用
收藏
页码:E301 / E311
页数:11
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