Amplification of the Steroidogenic Factor 1 Gene in Childhood Adrenocortical Tumors

Author:

Figueiredo Bonald C.1,Cavalli Luciane R.2,Pianovski Mara Albonei D.13,Lalli Enzo4,Sandrini Romolo5,Ribeiro Raul C.678,Zambetti Gerard9,DeLacerda Luiz5,Rodrigues Giovanna Assis1,Haddad Bassem R.2

Affiliation:

1. Department of Pediatrics, Center for Molecular Genetics and Cancer Research in Children (CEGEMPAC) (B.C.F., M.A.D.P., G.A.R.), Curitiba PR 80.030-110, Brazil

2. Department of Oncology and Institute for Molecular and Human Genetics/Lombardi Comprehensive Cancer Center (L.R.C., B.R.H.), Georgetown University, Washington, DC 20007

3. Department of Pediatrics, Division of Pediatric Hematology and Oncology (M.A.D.P.), Curitiba PR 80.030-110, Brazil

4. Institut de Génétique et de Biologie Moléculaire et Cellulaire Centre National de Ciencia y Tecnologia–Institut National de la Santé et de la Recherche Médicale (E.L.), Université Louis Pasteur, 67404 Illkirch, France

5. Department of Pediatrics, Division of Pediatric Endocrinology (R.S., L.D.), Federal University of Paraná, Curitiba PR 80.030-110, Brazil

6. Departments of Hematology-Oncology (R.C.R.), Memphis, Tennessee 38105

7. the International Outreach Program (R.C.R.), St. Jude Children’s Research Hospital, Memphis, Tennessee 38105

8. Department of Pediatrics (R.C.R.), University of Tennessee, College of Medicine, Memphis, Tennessee 38163

9. Biochemistry (G.Z.), Memphis, Tennessee 38105

Abstract

Southern Brazil has one of the highest incidences of childhood adrenocortical tumors (ACTs), occurring 10–15 times more frequently than worldwide estimates. The reasons for this increase remain elusive. In an attempt to further characterize the genetic changes in childhood ACTs, we recently detected a consistent gain of 9q (or a portion of it) in eight of nine cases of pediatric ACTs and amplification of 9q34 in the majority of these cases using comparative genomic hybridization. Other studies involving both childhood and adult ACTs have corroborated these findings. To follow up on these results, we examined whether the steroidogenic factor 1 (SF-1) gene, which is located in this chromosomal region and plays an important role in the development and function of the adrenal cortex is amplified in these ACT cases. We detected increased copy number of the SF-1 gene in all eight cases with 9q gain, suggesting an association between an increased copy number of the SF-1 gene and adrenocortical tumorigenesis.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference36 articles.

1. Childhood adrenocortical tumors.;Sandrini;J Clin Endocrinol Metab,1997

2. Extensive personal experience: adrenocortical tumors.;Latronico;J Clin Endocrinol Metab,1997

3. Comparative genomic hybridization analysis of adrenocortical tumors of childhood.;Figueiredo;J Clin Endocrinol Metab,1999

4. Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization.;James;Br J Cancer,1999

5. Adrenocortical carcinoma is characterized by a high frequency of chromosomal gains and high-level amplifications.;Dohna;Genes Chromosomes Cancer,2000

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