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No evidence for oncogenic mutations in the adrenocorticotropin receptor gene in human adrenocortical neoplasms

Journal Article · · Journal of Clinical Endocrinology and Metabolism
; ;  [1]
  1. National Inst. of Child Health and Human Development, Bethesda, MD (United States); and others

The mechanism(s) of tumorigenesis for the majority of adrenocortical neoplasms remain unknown. G-Protein-coupled receptors were recently proposed as candidate protooncogenes. That activating mutations of this class of receptors might be important for tumor induction or progression of endocrine neoplasms was strengthened by the recent identification of such mutations in hyperfunctioning thyroid adenomas. To examine whether the ACTH receptor (ACTH-R) gene could be an oncogene in human adrenocortical tumors, we amplified by the polymerase chain reaction and directly sequenced the entire exon of the ACTH-R gene in 25 adrenocortical tumors (17 adenomas and 8 carcinomas) and 2 adrenocortical cancer cell lines. We found no missense point mutations or even silent polymorphisms in any of the tumors and cell lines studied. We conclude that activating mutations of the ACTH-R gene do not represent a frequent mechanism of human adrenocortical tumorigenesis. 15 refs., 2 tabs.

OSTI ID:
283154
Journal Information:
Journal of Clinical Endocrinology and Metabolism, Journal Name: Journal of Clinical Endocrinology and Metabolism Journal Issue: 3 Vol. 80; ISSN JCEMAZ; ISSN 0021-972X
Country of Publication:
United States
Language:
English

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