
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/β-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.
Armadillo Domain Proteins, Tumor Suppressor Proteins, Mutation, Adrenal Cortex, Humans, Tumor Suppressor Protein p53, Cyclic AMP-Dependent Protein Kinases, Wnt Signaling Pathway, Adrenal Cortex Neoplasms
Armadillo Domain Proteins, Tumor Suppressor Proteins, Mutation, Adrenal Cortex, Humans, Tumor Suppressor Protein p53, Cyclic AMP-Dependent Protein Kinases, Wnt Signaling Pathway, Adrenal Cortex Neoplasms
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
