Liquid biopsy can detect BRCA2 gene variants in female dogs with mammary neoplasia.
Jéssica Rodrigues de OliveiraJucimara ColomboFrancine Moraes GonçalvesLucas Amoroso Lopes de CarvalhoDouglas Santos CostaTiago HenriqueAdriana Alonso NovaisMarina Gobbe Moschetta-PinheiroLuiz Gustavo de Almeida ChuffaLuiz Lehmann CoutinhoÁureo Evangelista SantanaDebora Aparecida Pires de Campos ZuccariPublished in: Veterinary and comparative oncology (2021)
Mammary tumours (MT) are one of the most prevalent malignancies in female dogs and women. Currently, molecular analyzes have shown that each tumour type presents its own genetic signature. In this context, liquid biopsy allows a comprehensive genetic characterisation of the tumour, enabling early diagnosis and personalised treatment of patients. In women, deleterious mutations inherited in BRCA2 gene are associated with an increased risk of breast cancer, resistance to therapies and worse prognosis. In female dogs, there are many divergent data on the involvement of BRCA2 gene with mammary carcinogenesis and what its pathogenic potential is. Therefore, the objective was to identify BRCA2 gene variants in 20 plasma DNA samples, from 10 newly diagnosed dogs with mammary cancer (RD), five control (CTR) and five mastectomized patients. Eleven single nucleotide polymorphisms (SNPs) were detected, most of them in the exon 11 and two indels (deletion/insertion) in the BRCA2 gene. However, there was no statistically significant difference in the SNPs/indels detected between the groups. In addition, only one SNP (p.T1425P) and one deletion (p.L2307del) were considered deleterious using in silico computational models. Interestingly, most common variants were present in the plasma of all groups, except for the Ile2614Thr, Ile2614Val, Thr1425Pro and p.L2307del variants. Thus, we observed that SNPs are common in the BRCA2 gene of female dogs with MT, with a similar condition identified in women with breast cancer. Liquid biopsy approach in dogs with MT is useful for genetic and therapeutic proposals.
Keyphrases
- copy number
- genome wide
- dna methylation
- breast cancer risk
- newly diagnosed
- ultrasound guided
- chronic kidney disease
- end stage renal disease
- adipose tissue
- pregnant women
- metabolic syndrome
- type diabetes
- machine learning
- single molecule
- gene expression
- pregnancy outcomes
- risk assessment
- data analysis
- skeletal muscle
- nucleic acid