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Cancer Cell ; 37(1): 123-134.e5, 2020 01 13.
Article in English | MEDLINE | ID: mdl-31883967

ABSTRACT

Pituitary neuroendocrine tumors (PitNETs) are common, with five main histological subtypes: lactotroph, somatotroph, and thyrotroph (POU1F1/PIT1 lineage); corticotroph (TBX19/TPIT lineage); and gonadotroph (NR5A1/SF1 lineage). We report a comprehensive pangenomic classification of PitNETs. PitNETs from POU1F1/PIT1 lineage showed an epigenetic signature of diffuse DNA hypomethylation, with transposable elements expression and chromosomal instability (except for GNAS-mutated somatotrophs). In TPIT lineage, corticotrophs were divided into three classes: the USP8-mutated with overt secretion, the USP8-wild-type with increased invasiveness and increased epithelial-mesenchymal transition, and the large silent tumors with gonadotroph transdifferentiation. Unexpected expression of gonadotroph markers was also found in GNAS-wild-type somatotrophs (SF1 expression), challenging the current definition of SF1/gonadotroph lineage. This classification improves our understanding and affects the clinical stratification of patients with PitNETs.


Subject(s)
Neuroendocrine Tumors/diagnosis , Neuroendocrine Tumors/genetics , Pituitary Neoplasms/diagnosis , Pituitary Neoplasms/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Cell Lineage , Chromosome Aberrations , DNA Methylation , Endopeptidases/metabolism , Endosomal Sorting Complexes Required for Transport/metabolism , Epigenesis, Genetic , Epigenome , Exome , Female , Humans , Male , Middle Aged , Mutation , Neoplasm Invasiveness , Neuroendocrine Tumors/pathology , Pituitary Gland/metabolism , Pituitary Neoplasms/pathology , Prognosis , Transcriptome , Ubiquitin Thiolesterase/metabolism , Young Adult
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