Abstract 184: Breed-associated differential microRNA expression in canine osteosarcoma

• Published in: Cancer research (Chicago, Ill.) Ill.), 2012-04, Vol.72 (8_Supplement), p.184-184
• Main Authors: Fenger, Joelle M., Volinia, Stefano, Jalkanen, Aimee, Ozer, H. Gulcin, Sarver, Aaron L., Subramanian, Subbaya, Breen, Matthew, Modiano, Jaime, London, Cheryl, Kisseberth, William
• Format: Article
• Language: English
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/1538-7445.AM2012-184

Introduction: MicroRNAs (miRNAs) are small non-coding RNAs that post-transcriptionally regulate gene expression. miRNAs are dysregulated in cancer, suggesting they play a role in tumorigenesis. Osteosarcoma (OSA) is the most common bone tumor in dogs, however, little is known regarding mechanisms underlying malignant transformation in these tumors. Breeds such as Rottweilers and Greyhounds are at higher risk for developing OSA, suggesting that heritable factors play a role in this disease. We hypothesize that dysregulation of miRNAs in canine OSA is associated with specific breeds. Methods: RNA was isolated by the Trizol (Invitrogen) method from a panel of seven normal canine tissues and 48 primary canine OSA tumors from Greyhound, Golden Retriever, Rottweiler, and mixed breed dogs. miRNA expression was analyzed using the NanoString nCounter human microRNA Expression Assay, interrogating the expression of 752 human miRNAs; 168 of whose mature sequences are 100% conserved between human and dog (Sanger miRBase V15). Samples were hybridized to reporter CodeSets, processed on the nCounter prep station, and scanned with the nCounter Digital Analyzer. Nanominer software was used to perform data normalization. Real time PCR was performed using Applied Biosystems Taqman miRNA assays. Normalization was performed with U6 snRNA and miRNA expression was calculated utilizing the comparative Ct method. P-values of