The Li-Fraumeni syndrome (LFS) is a rare autosomal dominant hereditary cancer syndrome, characterized by a wide spectrum of neoplasms, occurring in children and young adults. The identification of germline TP53 mutations in LFS has given rise to a number of in vitro studies using cultures of cancer cells and non-tumoral fibroblasts presenting...
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April 2010 (v1)Journal articleUploaded on: December 3, 2022
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August 30, 2007 (v1)Journal article
Steroidogenic Factor-1 (SF-1/Ad4BP; NR5A1), a nuclear receptor transcription factor, has a pivotal role in adrenal and gonadal development in humans and mice. A frequent feature of childhood adrenocortical tumors (ACT) is SF-1 amplification and overexpression. Here we show that an increased SF-1 dosage can by itself augment human adrenocortical...
Uploaded on: February 28, 2023 -
August 2007 (v1)Journal article
CONTEXT: Childhood adrenocortical tumors (ACTs) have a fetal adrenal phenotype and overexpress steroidogenic factor-1 (SF-1). Nephroblastoma overexpressed (NOV)/cysteine-rich protein 61/connective tissue growth factor/nephroblastoma overexpressed gene-3 mRNA is significantly down-regulated in childhood ACTs. OBJECTIVE: The objective of the...
Uploaded on: February 28, 2023