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Analysis of Endocrine Active and Clinically Silent Corticotropic Adenomas by in Situ Hybridization

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 1990 Aug 1
PMID 2167013
Citations 18
Authors
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Abstract

The distribution of pro-opiomelanocortin (POMC) messenger RNA (mRNA) in 7 functional and 17 clinically silent corticotropic adenomas was analyzed by in situ hybridization (ISH) with 35S-labeled oligonucleotide probes using formalin-fixed paraffin-embedded tissue sections cut from blocks that were in storage between 1 to 14 years. All 7 functional adenomas and 4 subtype 1 tumors had detectable POMC mRNA, while 3 of 6 subtype 2 and 1 of 7 subtype 3 silent adenomas contained detectable POMC mRNA. In situ hybridization analysis with an 35S-labeled beta-actin probe showed a positive hybridization signal in 22 of 22 cases, indicating that the absence of detectable POMC mRNA in some adenomas was not due to loss of the mRNAs during processing of the tissues or because of the age of the embedded tissue blocks. Northern hybridization analysis with the oligonucleotide probes in 2 normal pituitaries and an adenoma causing Cushing's disease detected a 1.2-Kb mRNA in all three tissues, indicating that the oligonucleotide probes were very specific. These results indicate that subtype 1 silent adenomas and clinically active adenomas associated with Cushing's disease contain POMC mRNA that is readily detectable by ISH in routinely processed tissue specimens, while only a few of the subtypes 2 and 3 adenomas have POMC mRNA that can be detected in paraffin blocks with the oligonucleotide probes used in this study.

Citing Articles

Corticotroph (Basophil) invasion of the pars nervosa in the human pituitary: Localization of proopiomelanocortin peptides, galanin and peptidylglycine α-amidating monooxygenase-like immunoreactivities.

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Silent corticotroph adenomas.

Cooper O Pituitary. 2014; 18(2):225-31.

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Silent corticogonadotroph adenomas: clinical and cellular characteristics and long-term outcomes.

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Classification and pathology of pituitary tumors.

Kontogeorgos G Endocrine. 2005; 28(1):27-35.

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Galectin-3 Expression in Functioning and Silent ACTH-Producing Adenomas.

Jin L, Riss D, Ruebel K, Kajita S, Scheithauer B, Horvath E Endocr Pathol. 2005; 16(2):107-14.

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