Peer-reviewed veterinary case report
PTPN11 gene mutation linked to histiocytic sarcoma in Bernese
By Thaiwong, T et al.·Published in Veterinary and comparative oncology·2018·Michigan State University, United States·View original on PubMed →
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Original publication title: Gain-of-function mutation in PTPN11 in histiocytic sarcomas of Bernese Mountain Dogs.
- Species:
- dog
Plain-English summary
A Bernese Mountain Dog diagnosed with a serious cancer called histiocytic sarcoma (HS) was found to have a specific genetic mutation in the PTPN11 gene. This mutation is linked to the development of HS, which is particularly common and aggressive in this breed. In a study of 30 Bernese Mountain Dogs with HS, researchers discovered that about 37% had this mutation, compared to only 9% in other breeds. Understanding this genetic link could help veterinarians develop better treatments for this type of cancer in Bernese Mountain Dogs.
People also search for: Bernese Mountain Dog cancer treatment · histiocytic sarcoma in dogs · PTPN11 mutation in dogs
Abstract
Histiocytic sarcoma (HS) is an aggressive malignant neoplasm of dendritic cell origin that is common in certain breeds of dogs. High prevalence of fatal, disseminated HS has been described in Bernese Mountain Dogs (BMDs). Support for genetic predisposition to develop HS has been presented in several studies, but to date, causative genetic events have not been reported. In addition, no driver mutations have been identified in tumours. Recently, E76K gain-of-function mutation in SHP2 encoded by the PTPN11 gene has been described in human histiocytic malignancies. In our study, we identified the PTPN11in HS of BMDs. Amplification of exon 3 of the PTPN11 gene followed by Sanger sequencing was used to detect the mutation and estimate the prevalence in HS from 30 BMDs, 13 Golden Retrievers and 10 other dog breeds. The overall prevalence of PTPN11in HS of BMDs was 36.67% compared with 8.69% in other breeds. No mutation was identified in normal tissues from 10 BMDs with HS that carried the mutation and 12 control dogs with no neoplastic disease, including 6 BMDs. Increased immunoreactivity for AKT, phosphorylated ERK1/2 and phosphorylated AKT in a small subset of BMDs with PTPN11suggests that a gain-of-function might be mediated by the ERK and AKT pathways. These data suggest PTPN11as an important driver mutation of HS in BMDs. This information may not only aid in unravelling the tumourigenic events associated with HS in BMDs, but also help in identifying more promising therapeutic strategies.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/28929581/