Canine transmissible venereal tumor

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Illustration of venereal granulomata on a dog's penis

A canine transmissible venereal tumor (CTVT), also known as a transmissible venereal tumor (TVT), canine transmissible venereal sarcoma (CTVS), sticker tumor and infectious sarcoma, is a

Syrian hamster
.

The tumor cells are themselves the infectious agents, and the tumors that form are not genetically related to the host dog.

sexually transmitted) pathogen.[4] Sequence analysis of the genome suggests it diverged from canids over 6,000 years ago; possibly much earlier.[4] Estimates from 2015 date its time of origin to about 11,000 years ago.[5] However, the most recent common ancestor of extant tumors is more recent: it probably originated 200 to 2,500 years ago.[1][6]

Canine TVTs were initially described by Russian veterinarian M.A. Novinsky (1841–1914) in 1876, when he demonstrated that the tumor could be transplanted from one dog to another by infecting them with tumor cells.[7]

Signs and symptoms

In male

lymph nodes.[10]

Pathology

Canine transmissible venereal tumors are

aneuploid but has characteristic marker chromosomes in all tumors collected in different geographic regions. Third, a long interspersed nuclear element (LINE-1) insertion near c-myc has been found in all tumors examined so far and can be used as a diagnostic marker to confirm that a tumor is a CTVT.[6][11]

Canine transmissible venereal tumors are most commonly seen in sexually active dogs in

lymph nodes,[citation needed] but can also be seen in the skin, brain, eye, liver, spleen, testicle, rectum and muscle.[17] A biopsy
is necessary for diagnosis.

The success of this single cell lineage, believed to be the longest continually propagated cell lineage in the world, can be attributed to the tumor's mode of transmission in a specific host system. Although direct contact is generally not a highly efficient mode of transfer, CTVTs take advantage of the popular sire effect of domestic dogs. A single male can produce dozens of litters over his lifetime, allowing the tumor to affect many more females than it could if a monogamous species were the host. Understanding the epidemiology of CTVTs could provide insights for populations that may experience CTVT exposure and information about disease prevalence.[citation needed]

Genetics

The CTVT cells have fewer

acrocentric, having a centromere very near to the end of the chromosome, while many of the CTVT chromosomes are metacentric or submetacentric, having a centromere nearer to the middle.[9]

All tumor cells of this type of cancer share extremely similar genetic code, often if not always unrelated to the DNA of their host.[6] In addition to the aforementioned c-myc insertion, a few other potential driver mutations have been identified.[18]

Treatment method

The tumor, when treated with the chemotherapy drug vincristine, regresses as the host immune system is activated. CCL5 may play an important role in the immune response.[19]

Treatment

Surgery may be difficult due to the location of these tumors. Surgery alone often leads to recurrence. Chemotherapy is very effective for TVTs. The prognosis for complete remission with chemotherapy is excellent.[20] The most common chemotherapy agents used are vincristine, vinblastine, and doxorubicin.[14] Radiotherapy may be required if chemotherapy does not work.[17]

References

  1. ^ a b Choi, Charles Q. (2006-08-10). "Contagious Canine Cancer Spread by Parasites". LiveScience. Archived from the original on 2006-08-20. Retrieved 2006-08-11.
  2. PMID 31160719
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  7. ^ a b Mello Martins, M.I.; de Souza, F. Ferreira; Gobello, C. (2005). "Canine transmissible venereal tumor: Etiology, pathology, diagnosis and treatment". Recent Advances in Small Animal Reproduction. Retrieved 2006-05-25.
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  16. ^ "Canine Transmissible Venereal Tumor: Introduction". The Merck Veterinary Manual. 2006. Retrieved 2007-04-24.
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    PMID 9826280
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External links