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Molecular Alterations in Dog Pheochromocytomas and Paragangliomas.

Authors :
Korpershoek E
Dieduksman DAER
Grinwis GCM
Day MJ
Reusch CE
Hilbe M
Fracassi F
Krol NMG
Uitterlinden AG
de Klein A
Eussen B
Stoop H
de Krijger RR
Galac S
Dinjens WNM
Source :
Cancers [Cancers (Basel)] 2019 Apr 30; Vol. 11 (5). Date of Electronic Publication: 2019 Apr 30.
Publication Year :
2019

Abstract

8658860258318000Recently, genetic alterations in the genes encoding succinate dehydrogenase subunit B and D ( SDHB and SDHD ) were identified in pet dogs that presented with spontaneously arising pheochromocytomas (PCC) and paragangliomas (PGL; together PPGL), suggesting dogs might be an interesting comparative model for the study of human PPGL. To study whether canine PPGL resembled human PPGL, we investigated a series of 50 canine PPGLs by immunohistochemistry to determine the expression of synaptophysin (SYP), tyrosine hydroxylase (TH) and succinate dehydrogenase subunit A (SDHA) and B (SDHB). In parallel, 25 canine PPGLs were screened for mutations in SDHB and SDHD by Sanger sequencing. To detect large chromosomal alterations, single nucleotide polymorphism (SNP) arrays were performed for 11 PPGLs, including cases for which fresh frozen tissue was available. The immunohistochemical markers stained positive in the majority of canine PPGLs. Genetic screening of the canine tumors revealed the previously described variants in four cases; SDHB p.Arg38Gln ( n = 1) and SDHD p.Lys122Arg ( n = 3). Furthermore, the SNP arrays revealed large chromosomal alterations of which the loss of chromosome 5, partly homologous to human chromosome 1p and chromosome 11, was the most frequent finding (100% of the six cases with chromosomal alterations). In conclusion, canine and human PPGLs show similar genomic alterations, suggestive of common interspecies PPGL-related pathways.<br />Competing Interests: The authors declare no conflict of interest

Details

Language :
English
ISSN :
2072-6694
Volume :
11
Issue :
5
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
31052272
Full Text :
https://doi.org/10.3390/cancers11050607