TY - JOUR
T1 - Steroids-producing nodules
T2 - a two-layered adrenocortical nodular structure as a precursor lesion of cortisol-producing adenoma
AU - Fukumoto, Tazuru
AU - Umakoshi, Hironobu
AU - Iwahashi, Norifusa
AU - Ogasawara, Tatsuki
AU - Yokomoto-Umakoshi, Maki
AU - Kaneko, Hiroki
AU - Fujita, Masamichi
AU - Uchida, Naohiro
AU - Nakao, Hiroshi
AU - Kawamura, Namiko
AU - Matsuda, Yayoi
AU - Sakamoto, Ryuichi
AU - Miyazawa, Takashi
AU - Seki, Masahide
AU - Eto, Masatoshi
AU - Oda, Yoshinao
AU - Suzuki, Yutaka
AU - Ogawa, Seishi
AU - Ogawa, Yoshihiro
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/5
Y1 - 2024/5
N2 - Background: The human adrenal cortex consists of three functionally and structurally distinct layers; zona glomerulosa, zona fasciculata (zF), and zona reticularis (zR), and produces adrenal steroid hormones in a layer-specific manner; aldosterone, cortisol, and adrenal androgens, respectively. Cortisol-producing adenomas (CPAs) occur mostly as a result of somatic mutations associated with the protein kinase A pathway. However, how CPAs develop after adrenocortical cells acquire genetic mutations, remains poorly understood. Methods: We conducted integrated approaches combining the detailed histopathologic studies with genetic, RNA-sequencing, and spatially resolved transcriptome (SRT) analyses for the adrenal cortices adjacent to human adrenocortical tumours. Findings: Histopathological analysis revealed an adrenocortical nodular structure that exhibits the two-layered zF- and zR-like structure. The nodular structures harbour GNAS somatic mutations, known as a driver mutation of CPAs, and confer cell proliferative and autonomous steroidogenic capacities, which we termed steroids-producing nodules (SPNs). RNA-sequencing coupled with SRT analysis suggests that the expansion of the zF-like structure contributes to the formation of CPAs, whereas the zR-like structure is characterised by a macrophage-mediated immune response. Interpretation: We postulate that CPAs arise from a precursor lesion, SPNs, where two distinct cell populations might contribute differently to adrenocortical tumorigenesis. Our data also provide clues to the molecular mechanisms underlying the layered structures of human adrenocortical tissues. Funding: KAKENHI, The Uehara Memorial Foundation, Daiwa Securities Health Foundation, Kaibara Morikazu Medical Science Promotion Foundation, Secom Science and Technology Foundation, ONO Medical Research Foundation, and Japan Foundation for Applied Enzymology.
AB - Background: The human adrenal cortex consists of three functionally and structurally distinct layers; zona glomerulosa, zona fasciculata (zF), and zona reticularis (zR), and produces adrenal steroid hormones in a layer-specific manner; aldosterone, cortisol, and adrenal androgens, respectively. Cortisol-producing adenomas (CPAs) occur mostly as a result of somatic mutations associated with the protein kinase A pathway. However, how CPAs develop after adrenocortical cells acquire genetic mutations, remains poorly understood. Methods: We conducted integrated approaches combining the detailed histopathologic studies with genetic, RNA-sequencing, and spatially resolved transcriptome (SRT) analyses for the adrenal cortices adjacent to human adrenocortical tumours. Findings: Histopathological analysis revealed an adrenocortical nodular structure that exhibits the two-layered zF- and zR-like structure. The nodular structures harbour GNAS somatic mutations, known as a driver mutation of CPAs, and confer cell proliferative and autonomous steroidogenic capacities, which we termed steroids-producing nodules (SPNs). RNA-sequencing coupled with SRT analysis suggests that the expansion of the zF-like structure contributes to the formation of CPAs, whereas the zR-like structure is characterised by a macrophage-mediated immune response. Interpretation: We postulate that CPAs arise from a precursor lesion, SPNs, where two distinct cell populations might contribute differently to adrenocortical tumorigenesis. Our data also provide clues to the molecular mechanisms underlying the layered structures of human adrenocortical tissues. Funding: KAKENHI, The Uehara Memorial Foundation, Daiwa Securities Health Foundation, Kaibara Morikazu Medical Science Promotion Foundation, Secom Science and Technology Foundation, ONO Medical Research Foundation, and Japan Foundation for Applied Enzymology.
KW - Adrenal androgen
KW - Adrenocortical tumorigenesis
KW - Clonal expansion
KW - Cortisol-producing adenoma
KW - Cushing's syndrome
KW - GNAS
UR - http://www.scopus.com/inward/record.url?scp=85192725107&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85192725107&partnerID=8YFLogxK
U2 - 10.1016/j.ebiom.2024.105087
DO - 10.1016/j.ebiom.2024.105087
M3 - Article
C2 - 38570222
AN - SCOPUS:85192725107
SN - 2352-3964
VL - 103
JO - EBioMedicine
JF - EBioMedicine
M1 - 105087
ER -