Genomic analysis to study cancer in dogs can help develop new therapies for human cancers


Using genomic analysis to study cancer in dogs can help develop new therapies for humans with cancer, according to a proof-of-concept study led by the National Cancer Institute (NCI) and the Translational Genomics Research Institute (TGen).

Pure-breed dogs, whose genetics have been standardized by hundreds of years of human intervention, provide highly predictable genetic models useful in designing clinical trials, in which specific drugs are matched to the molecular profiles of human patients, according to the study published today in the scientific journal PLOS ONE.

“Our canine companions are not only ‘Man’s Best Friend,’ but our study shows that dogs also can help human patients pursue battles against various types of cancer,” said Dr. Jeffrey Trent, TGen President and Research Director and the study’s senior author. “Not only do dogs with cancer benefit from this research, but people do, as well.”

While there are, relatively, many genetic differences among humans with the same type of cancer, there are far fewer genetic differences among dogs of the same breed, making it vastly easier to identify and study the genes driving canine cancers.

The process of integrating naturally occurring cancers in dogs into the general studies of human cancer biology and therapy is known as comparative oncology. The identification of specific drugs to treat individuals based on their specific genetic or molecular make-up is often referred to as personalized medicine, or PMed.

Genetic samples from 31 dogs were analyzed in the proof-of-concept study organized under NCI’s Comparative Oncology Trials Consortium (COTC). Genetic samples were derived for this study from tumor biopsy samples. No dogs were harmed in any way in this clinical study.

“Complex models are needed to effectively evaluate PMed study designs, and this proof-of-concept trial validates the dog with cancer as a model for clinical evaluation of novel PMed approaches,” said Dr. Melissa Paoloni, the study’s lead author and former director of the COTC. “Comparative oncology models have the potential to expedite this evaluation and lead advancements in personalized medicine.”