Genetics of Adrenocortical Development and Tumors

被引:19
|
作者
Lodish, Maya [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, NIH, Bldg 10,Room 9D42,10 Ctr Dr,MSC 1830, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Adrenal development; Adrenocortical carcinoma; Ontogenesis; Zonation; Signaling; Pathway; Genetic; Driver mutation; MACRONODULAR ADRENAL-HYPERPLASIA; PROTEIN-KINASE-A; ALDOSTERONE-PRODUCING ADENOMAS; BECKWITH-WIEDEMANN SYNDROME; SOMATIC MUTATIONS; ARMC5; MUTATIONS; REGULATORY SUBUNIT; HEREDITARY LEIOMYOMATOSIS; GENOMIC CHARACTERIZATION; CATALYTIC SUBUNIT;
D O I
10.1016/j.ecl.2017.01.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This article links the understanding of developmental physiology of the adrenal cortex to adrenocortical tumor formation. Many molecular mechanisms that lead to formation of adrenocortical tumors have been discovered via next-generation sequencing approaches. The most frequently mutated genes in adrenocortical tumors are also factors in normal adrenal development and homeostasis, including those that alter the p53 and Wnt/beta-catenin pathways. In addition, dysregulated protein kinase A signaling and ARMC5 mutations have been identified as key mediators of adrenocortical tumorigenesis. The growing understanding of genetic changes that orchestrate adrenocortical development and disease pave the way for potential targeted treatment strategies.
引用
收藏
页码:419 / +
页数:16
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