ACTH-independent production of 11-oxygenated androgens and glucocorticoids in an adrenocortical adenoma

Author:

Kitamura Takuya1,Blinder Amy R2,Nanba Kazutaka123ORCID,Tsuiki Mika1,Mishina Mutsuki4,Okuno Hiroshi4,Moriyoshi Koki5,Yamazaki Yuto6,Sasano Hironobu6,Yoneyama Keisuke7,Udager Aaron M8910,Rainey William E211,Yasoda Akihiro12,Satoh-Asahara Noriko3,Tagami Tetsuya13

Affiliation:

1. Department of Endocrinology and Metabolism, National Hospital Organization Kyoto Medical Center , Kyoto, Japan

2. Department of Molecular and Integrative Physiology, University of Michigan , Ann Arbor, Michigan, USA

3. Department of Endocrinology, Metabolism, and Hypertension Research, Clinical Research Institute , Kyoto, Japan

4. Department of Urology, National Hospital Organization Kyoto Medical Center , Kyoto, Japan

5. Department of Diagnostic Pathology, National Hospital Organization Kyoto Medical Center , Kyoto, Japan

6. Department of Pathology, Tohoku University Graduate School of Medicine , Sendai, Japan

7. Aska Pharma Medical Co. Ltd. , Fujisawa, Japan

8. Department of Pathology, University of Michigan , Ann Arbor, Michigan, USA

9. Michigan Center for Translational Pathology, University of Michigan , Ann Arbor, Michigan, USA

10. Rogel Cancer Center, University of Michigan , Ann Arbor, Michigan, USA

11. Division of Metabolism, Endocrinology, and Diabetes, University of Michigan , Ann Arbor, Michigan, USA

12. Clinical Research Institute, National Hospital Organization Kyoto Medical Center , Kyoto, Japan

Abstract

Abstract Although excess production of androgens and glucocorticoids has often been observed in adrenocortical carcinomas, adrenocortical adenoma with such hormonal activity is rare. Herein, we report a 41-year-old woman who presented with hyperandrogenemia and mild autonomous cortisol secretion with an undetectable level of adrenocorticotropic hormone. Imaging demonstrated a 6 cm left adrenal tumor. The histologic diagnosis of the resected adrenal tumor was adrenocortical adenoma. Pre- and post-operative serum samples were used for steroid profiling with liquid chromatography-tandem mass spectrometry (LC-MS/MS). LC-MS/MS analysis of pre-operative serum revealed an abnormal buildup of steroid precursors and androgens. Importantly, circulating levels of 11-oxygenated androgens, including 11β-hydroxytestosterone (11OHT) and 11-ketotestosterone (11KT), were highly elevated. Both androgen and glucocorticoid levels significantly decreased post-operatively. Immunohistochemical analysis of steroidogenic enzymes and cofactor protein supported the tumor's ability to directly produce 11OHT and 11KT. This study is the first to describe and characterize an adrenocortical adenoma that co-secretes glucocorticoids and 11-oxygenated androgens. Significance statement Due to its rarity, biochemical and histologic characteristics of androgen and glucocorticoid co-secreting adrenocortical adenomas are largely unknown. Herein, we report a case of adrenocortical adenoma that caused marked hyperandrogenemia and mild autonomous cortisol secretion. In this study, we investigated serum steroid profiles using liquid chromatography-tandem mass spectrometry (LC-MS/MS) and histologic characteristics of the resected tumor. LC-MS/MS revealed highly elevated levels of 11-oxygenated androgens which have not been well studied in adrenal tumors. The expression patterns of steroidogenic enzymes determined by immunohistochemistry supported the results of steroid profiling and suggested the capacity of the tumor cells to produce 11-oxygenated androgens. Measurement of 11-oxygenated steroids should facilitate a better understanding of androgen-producing adrenocortical neoplasms.

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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