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Breast cancer: Tumor marker same in dogs and humans

Date:
April 18, 2011
Source:
University of Veterinary Medicine -- Vienna
Summary:
Researchers were surprised to find that dogs and humans share a common tumor marker. The researchers uncovered a molecule, the CEA (carcinoembryonic antigen) receptor, that is almost identical in the two species. The result could lead to the rapid development of new therapies for dogs and humans.

The dog may be 'man's best friend' but even so it comes as a surprise that the two species share a common tumour marker. This finding comes from a joint study between scientists of the Vetmeduni Vienna and the MedUni Wien, headed by Erika Jensen-Jarolim. The researchers looked for similarities in breast cancer of dogs and women, focussing on the tumour marker CEA (carcinoembryonic antigen). They uncovered a molecule, the CEA receptor, that turned out to be essentially identical in the two species. The result could lead to the rapid development of new therapeutic methods for use in dogs and humans.

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Despite steadily improving methods for its diagnosis and treatment, cancer still represents one of the most frequent causes of death in humans. What is less well known is that this also holds true for pets such as dogs. Each year, an estimated 4,000 dogs in Austria develop cancer and about half the dogs over 10 years old die because they develop a carcinoma that is biologically similar to a human tumour.

CEA is one of the most important markers for tumours. It is found in high concentrations in cancer patients and is thought to have a signalling function in tumour cells, which it effects via a specific receptor molecule, the CEA receptor. Jenson-Jarolim's work now shows that CEA itself is constructed extremely differently in dogs and humans: the antigen represents a particularly heterogeneous and complex system of different families of molecules. In contrast, however, the CEA receptor is essentially identical in the two species. The scientists explain the finding by proposing that the CEA receptor is a very old molecule in evolutionary terms and that because of its biological importance it has remained practically unchanged in the two species.

Subsequent work will address the nature of the molecules that bind to the receptor in human breast cancer or in cancer of the milk glands in dogs. The hope is that the knowledge can be exploited for new therapeutic approaches. Jensen-Jarolim is excited by the prospect. "Because dogs have shorter life-spans than humans, similar processes place on a shorter time-scale. This means that research in dogs gives faster results. By means of comparative research on the two species -- so-called comparative medicine -- it might be possible to develop a new generation of diagnostic and therapeutic procedures much, much faster. And these may be applicable both to humans and to animals."


Story Source:

The above story is based on materials provided by University of Veterinary Medicine -- Vienna. Note: Materials may be edited for content and length.


Journal Reference:

  1. Marlene Weichselbaumer, Michael Willmann, Martin Reifinger, Josef Singer, Erika Bajna, Yuriy Sobanov, Diana Mechtcherikova, Edgar Selzer, Johann G. Thalhammer, Robert Kammerer, Erika Jensen-Jarolim. Phylogenetic discordance of human and canine carcinoembryonic antigen (CEA, CEACAM) families, but striking identity of the CEA receptors will impact comparative oncology studies.. PLoS Currents, 2011; 3: RRN1223 DOI: 10.1371/currents.RRN1223

Cite This Page:

University of Veterinary Medicine -- Vienna. "Breast cancer: Tumor marker same in dogs and humans." ScienceDaily. ScienceDaily, 18 April 2011. <www.sciencedaily.com/releases/2011/04/110418093844.htm>.
University of Veterinary Medicine -- Vienna. (2011, April 18). Breast cancer: Tumor marker same in dogs and humans. ScienceDaily. Retrieved December 20, 2014 from www.sciencedaily.com/releases/2011/04/110418093844.htm
University of Veterinary Medicine -- Vienna. "Breast cancer: Tumor marker same in dogs and humans." ScienceDaily. www.sciencedaily.com/releases/2011/04/110418093844.htm (accessed December 20, 2014).

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