Tumor Shrinkage by Metyrapone in Cushing Disease Exhibiting Glucocorticoid-Induced Positive Feedback.

3D culture Cushing disease metyrapone positive feedback tumor shrinkage

Journal

Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997

Informations de publication

Date de publication:
01 Jun 2021
Historique:
received: 30 10 2020
entrez: 1 6 2021
pubmed: 2 6 2021
medline: 2 6 2021
Statut: epublish

Résumé

Paradoxical increases in serum cortisol in the dexamethasone suppression test (DST) have been rarely observed in Cushing disease (CD). Its pathophysiology and prevalence remain unclear. A 62-year-old woman with suspected CD showed paradoxical increases in cortisol after both 1-mg and 8-mg DST (1.95-fold and 2.52-fold, respectively). The initiation of metyrapone paradoxically decreased plasma adrenocorticotropic hormone (ACTH) levels and suppressed cortisol levels. Moreover, the pituitary tumor considerably shrank during metyrapone treatment. The resected tumor tissue was enzymatically digested, dispersed, and embedded into Matrigel as 3D cultured cells. ACTH levels in the media were measured. In this tumor culture, ACTH levels increased 1.3-fold after dexamethasone treatment ( A cross-sectional, retrospective, multicenter study that included 92 patients with CD who underwent both low-dose and high-dose DST from 2014 to 2020 was performed. Eight cases (8.7%) showed an increase in serum cortisol after both low-dose and high-dose DST. This is the first report of a patient with glucocorticoid (GC)-driven positive feedback CD who showed both ACTH suppression and tumor shrinkage by metyrapone. Our cohort study revealed that 8.7% of patients with CD patients possibly possess GC-driven positive-feedback systems, thereby suggesting the presence of a new subtype of CD that is different from the majority of CD cases. The mechanisms exhibiting GC positive feedback in CD and the therapeutic approach for these patients remain to be investigated.

Identifiants

pubmed: 34061117
doi: 10.1210/jendso/bvab055
pii: bvab055
pmc: PMC8143664
doi:

Types de publication

Journal Article

Langues

eng

Pagination

bvab055

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society.

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Auteurs

Yasutaka Tsujimoto (Y)

Division of Diabetes and Endocrinology, Akashi Medical Center Hospital, Akashi 674-0063, Japan.

Hiroki Shichi (H)

Division of Diabetes and Endocrinology, Kobe University School of Medicine, Kobe 650-0017, Japan.

Hidenori Fukuoka (H)

Division of Diabetes and Endocrinology, Kobe University Hospital, Kobe 650-0017, Japan.

Masaaki Yamamoto (M)

Division of Diabetes and Endocrinology, Kobe University Hospital, Kobe 650-0017, Japan.

Itsuko Sato (I)

Department of Clinical Laboratory, Kobe University Hospital, Kobe 650-0017, Japan.

Takamitsu Imanishi (T)

Department of Clinical Laboratory, Kobe University Hospital, Kobe 650-0017, Japan.

Tomoaki Nakamura (T)

Division of Diabetes and Endocrinology, Akashi Medical Center Hospital, Akashi 674-0063, Japan.

Naoko Inoshita (N)

Department of Pathology, Tokyo Metropolitan Geriatric Medical Center, Tokyo 173-0015, Japan.

Atsushi Ishida (A)

Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0088, Japan.

Shozo Yamada (S)

Pituitary Center, Moriyama Memorial Hospital, Tokyo 134-0088, Japan.
Department of Hypothalamic and Pituitary Surgery, Toranomon Hospital, Tokyo 105-8470, Japan.

Yutaka Takahashi (Y)

Division of Diabetes and Endocrinology, Kobe University School of Medicine, Kobe 650-0017, Japan.

Kazuo Chihara (K)

Division of Diabetes and Endocrinology, Akashi Medical Center Hospital, Akashi 674-0063, Japan.

Classifications MeSH