Back to Search Start Over

Calcitonin receptor expression in medullary thyroid carcinoma

Authors :
Virginia Cappagli
Catarina Soares Potes
Luciana Bueno Ferreira
Catarina Tavares
Catarina Eloy
Rossella Elisei
Manuel Sobrinho-Simões
Peter J. Wookey
Paula Soares
Source :
PeerJ, Vol 5, p e3778 (2017)
Publication Year :
2017
Publisher :
PeerJ Inc., 2017.

Abstract

Background Calcitonin expression is a well-established marker for medullary thyroid carcinoma (MTC); yet the role of calcitonin receptor (CTR), its seven-transmembrane G-protein coupled receptor, remains to be established in C-cells derived thyroid tumors. The aim of this work was to investigate CTR expression in MTC and to correlate such expression with clinicopathological features in order to evaluate its possible role as a prognostic indicator of disease aggressiveness and outcome. Methods Calcitonin receptor expression was analyzed in a series of 75 MTCs by immunohistochemistry, and by qPCR mRNA quantification in specimens from four patients. Statistical tests were used to evaluate the correlation between CTR expression and the clinicopathological and molecular characteristics of patients and tumors. Results Calcitonin receptor expression was detected in 62 out of 75 samples (82.7%), whereas 13 of the 75 samples (17.3%) were completely negative. CTR expression was significantly associated with expression of cytoplasmatic phosphatase and tensin homologue deleted on chromosome 10 and osteopontin, as well as with wild type RET/RAS genes and absence of tumor stroma, suggesting that CTR expression do not associate with clinicopathological signs of worse prognosis. Discussion Calcitonin receptor expression appears to be associated in MTC with more differentiated status of the neoplastic cells.

Details

Language :
English
ISSN :
21678359
Volume :
5
Database :
Directory of Open Access Journals
Journal :
PeerJ
Publication Type :
Academic Journal
Accession number :
edsdoj.30ce162084e548d2b5bb021c3be17aab
Document Type :
article
Full Text :
https://doi.org/10.7717/peerj.3778