Human tumors associated with Carney complex and germline PRKAR1A mutations:: a protein kinase A disease!

被引:65
作者
Stergiopoulos, SG [1 ]
Stratakis, CA [1 ]
机构
[1] NICHD, DEP, Sect Endocrinol & Genet, NIH, Bethesda, MD 20892 USA
关键词
protein kinase A; regulatory subunit; Carney complex; chromosome; 17; deletion; tumor suppressor gene;
D O I
10.1016/S0014-5793(03)00452-6
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
Carney complex (CNC) is a multiple neoplasia syndrome that consists of endocrine (thyroid, pituitary, adrenocortical and gonadal), non-endocrine (myxomas, nevi and other cutaneous pigmented lesions), and neural (schwannomas) tumors. Primary pigmented nodular adrenocortical disease (PPNAD) is the most common endocrine manifestation of CNC and the only inherited form of Cushing syndrome known to date. In the search of genes responsible for CNC, two chromosomal loci were identified; one (17q22-24) harbored the gene encoding the type I-alpha regulatory subunit (RIalpha) of protein kinase A (PKA), PRKAR1A, a critical component of the cAMP signaling pathway. Here we review CNC and the implications of this discovery for the cAMP and/or PKA's involvement in human tumorigenesis. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:59 / 64
页数:6
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