Comprehensive Genomic Profiling of Androgen-Receptor-Negative Canine Prostate Cancer

• Main Authors: Renée Laufer-Amorim, Carlos Eduardo Fonseca-Alves, Rolando Andre Rios Villacis, Sandra Aparecida Drigo Linde, Marcio Carvalho, Simon Jonas Larsen, Fabio Albuquerque Marchi, Silvia Regina Rogatto
• Format: Article
• Language: English
• Published: MDPI AG 2019-03-01
• Series: International Journal of Molecular Sciences
• Subjects: dog; prostate cancer; proliferative inflammatory atrophy; microarray; copy number alteration; comparative oncology
• Online Access: https://www.mdpi.com/1422-0067/20/7/1555

Canine carcinomas have been considered natural models for human diseases; however, the genomic profile of canine prostate cancers (PCs) has not been explored. In this study, 14 PC androgen-receptor-negative cases, 4 proliferative inflammatory atrophies (PIA), and 5 normal prostate tissues were investigated by array-based comparative genomic hybridization (aCGH). Copy number alterations (CNAs) were assessed using the Canine Genome CGH Microarray 4 &#215; 44K (Agilent Technologies). Genes covered by recurrent CNAs were submitted to enrichment and cross-validation analysis. In addition, the expression levels of <i>TP53</i>, <i>MDM2</i> and <i>ZBTB4</i> were evaluated in an independent set of cases by qPCR. PC cases presented genomic complexity, while PIA samples had a small number of CNAs. Recurrent losses covering well-known tumor suppressor genes, such as <i>ATM</i>, <i>BRCA1</i>, <i>CDH1</i>, <i>MEN1</i> and <i>TP53</i>, were found in PC. The in silico functional analysis showed several cancer-related genes associated with canonical pathways and interaction networks previously described in human PC. The <i>MDM2</i>, <i>TP53</i>, and <i>ZBTB4</i> copy number alterations were translated into altered expression levels. A cross-validation analysis using The Cancer Genome Atlas (TCGA) database for human PC uncovered similarities between canine and human PCs. Androgen-receptor-negative canine PC is a complex disease characterized by high genomic instability, showing a set of genes with similar alterations to human cancer.