Ontology highlight
ABSTRACT:
SUBMITTER: Berthon A
PROVIDER: S-EPMC5235969 | biostudies-literature | 2017 Feb
REPOSITORIES: biostudies-literature
Berthon Annabel A Faucz Fabio F Bertherat Jerome J Stratakis Constantine A CA
Molecular and cellular endocrinology 20160824
Mutations in ARMC5 gene have been recently identified as the main cause of Primary Macronodular Adrenocortical Hyperplasia (PMAH). PMAH patients have an ARMC5 germline mutation and, in addition, somatic tissue-specific mutations. This is consistent with the two-hit hypothesis of tumorigenesis and suggests that ARMC5 may be a tumor suppressor gene. As its function is still unclear, we analyzed the expression of the four ARMC5 isoforms in 46 normal human tissues. This showed that at least one ARMC ...[more]