Expression of steroidogenic factor 1 in canine cortisol-secreting adrenocortical tumors and normal adrenals

Publication date

2014

Authors

Galac, SaraORCID 0000-0002-4831-4995ISNI 0000000393573977
Kool, Miriam M JISNI 0000000506789572
van den Berg, Marit F.ORCID 0000-0002-2016-119XISNI 0000000512624635
Mol, Jan AISNI 0000000109723801
Kooistra, Hans SISNI 0000000394691609

Editors

Advisors

Supervisors

Document Type

Article
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License

taverne

Abstract

We report on a screening for the relative messenger RNA (mRNA) and protein expression of steroidogenic factor 1 (SF-1) in normal canine adrenals (n = 10) and cortisol-secreting adrenocortical tumors (11 adenomas and 26 carcinomas). The relative mRNA expression of SF-1 was determined by quantitative real-time polymerase chain reaction analysis and revealed no differences between normal adrenals, adenomas, and carcinomas. Immunohistochemistry demonstrated SF-1 protein expression in a nuclear pattern throughout the normal adrenal cortex and a predominantly nuclear staining pattern in adrenocortical tumors. Of the 15 dogs available for follow up, 7 dogs developed hypercortisolism within 2.5 yr after adrenalectomy, with metastatic disease in 6 dogs and adrenocortical tumor regrowth in 1 dog. The relative SF-1 mRNA expression in dogs with early recurrence was greater (2.46-fold, P = 0.020) than in dogs in remission for at least 2.5 yr after adrenalectomy. In conclusion, we demonstrated the presence of SF-1 expression in normal canine adrenals and adrenocortical tumors. The high SF-1 mRNA expression in carcinomas with early recurrence might indicate its value as a prognostic marker, as well as its potential for therapeutic development.

Keywords

Cushing’s syndrome, Metastasis, Adrenal, Dog, Taverne

Citation

Galac, S, Kool, M M J, van den Berg, M F, Mol, J A & Kooistra, H S 2014, 'Expression of steroidogenic factor 1 in canine cortisol-secreting adrenocortical tumors and normal adrenals', Domestic Animal Endocrinology, vol. 49, pp. 1-5. https://doi.org/10.1016/j.domaniend.2014.04.002