Canine Transmissible Venereal Tumor

Canine Transmissible Venereal Tumor (CTVT) is a contagious neoplasm which is transmitted between dogs as an allogenic graft. The neoplastic cells originate from normal cell that has undergone tumourigenic transformation as a result of genetic mutations. It is the oldest and most prolific neoplasm li...

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Main Authors: Sathish Kumar M1, Poobitha S 2, Ramajayan P 3
Format: Article in Journal/Newspaper
Language:unknown
Published: Zenodo 2022
Subjects:
Online Access:https://doi.org/10.5281/zenodo.7422158
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spelling ftzenodo:oai:zenodo.org:7422158 2024-09-15T17:46:16+00:00 Canine Transmissible Venereal Tumor Sathish Kumar M1 Poobitha S 2 Ramajayan P 3 2022-12-10 https://doi.org/10.5281/zenodo.7422158 unknown Zenodo https://zenodo.org/communities/thescienceworld https://doi.org/10.5281/zenodo.7422157 https://doi.org/10.5281/zenodo.7422158 oai:zenodo.org:7422158 info:eu-repo/semantics/openAccess Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode The Science World a monthly e magazine, 2(12), 2070-2075, (2022-12-10) info:eu-repo/semantics/article 2022 ftzenodo https://doi.org/10.5281/zenodo.742215810.5281/zenodo.7422157 2024-07-25T13:48:03Z Canine Transmissible Venereal Tumor (CTVT) is a contagious neoplasm which is transmitted between dogs as an allogenic graft. The neoplastic cells originate from normal cell that has undergone tumourigenic transformation as a result of genetic mutations. It is the oldest and most prolific neoplasm lineage known in nature, which evolved 11,000 years. CTVT affects the genital and extra-genital sites of both sexes and is transmitted by allogenic transfer of viable neoplastic cells during coitus or by biting, scratching or licking the affected areas by the transplantation of tumor cells. It is most common in dogs aged 2 to 5 years and the incidence is high in females compared to males. It is homogenously distributed in India and reported in all parts of the world, except Antarctica. CTVT escape from the host immune mechanism by not expressing the MHC molecules on the cell surface. The neoplasm undergoes three different stages includes progressive phase, stable phase and regressive phase. Clinical signs include bloody discharge from the genital region and cauliflower- like growth in the genital region of both sexes. Diagnosis of this tumor by examination of cytology, histopathology and molecular confirmation. Cytology is the gold standard method of diagnosis, in which neoplastic cells are round with oval or round nucleus with one or two nucleoli and cytoplasm have punctuate vacuoles and fine granules. In histopathology, CTVT characteristically presents as a group of compact masses of diffusely arranged round or polyhedral cells with a centrally located nucleus and having punctuate vacuoles in the cytoplasm which are supported by thin trabeculae of fibrovascular tissue. CTVT cells are aneuploid, having stable karyotype of 57–59 chromosomes compared to normal chromosome number of dog. The CTVT cells are marked by the presence of Long Interspersed Nuclear Element (LINE-1) insertion close to the c-myc gene and homozygous loss of the CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) gene. Article in Journal/Newspaper Antarc* Antarctica Zenodo
institution Open Polar
collection Zenodo
op_collection_id ftzenodo
language unknown
description Canine Transmissible Venereal Tumor (CTVT) is a contagious neoplasm which is transmitted between dogs as an allogenic graft. The neoplastic cells originate from normal cell that has undergone tumourigenic transformation as a result of genetic mutations. It is the oldest and most prolific neoplasm lineage known in nature, which evolved 11,000 years. CTVT affects the genital and extra-genital sites of both sexes and is transmitted by allogenic transfer of viable neoplastic cells during coitus or by biting, scratching or licking the affected areas by the transplantation of tumor cells. It is most common in dogs aged 2 to 5 years and the incidence is high in females compared to males. It is homogenously distributed in India and reported in all parts of the world, except Antarctica. CTVT escape from the host immune mechanism by not expressing the MHC molecules on the cell surface. The neoplasm undergoes three different stages includes progressive phase, stable phase and regressive phase. Clinical signs include bloody discharge from the genital region and cauliflower- like growth in the genital region of both sexes. Diagnosis of this tumor by examination of cytology, histopathology and molecular confirmation. Cytology is the gold standard method of diagnosis, in which neoplastic cells are round with oval or round nucleus with one or two nucleoli and cytoplasm have punctuate vacuoles and fine granules. In histopathology, CTVT characteristically presents as a group of compact masses of diffusely arranged round or polyhedral cells with a centrally located nucleus and having punctuate vacuoles in the cytoplasm which are supported by thin trabeculae of fibrovascular tissue. CTVT cells are aneuploid, having stable karyotype of 57–59 chromosomes compared to normal chromosome number of dog. The CTVT cells are marked by the presence of Long Interspersed Nuclear Element (LINE-1) insertion close to the c-myc gene and homozygous loss of the CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) gene.
format Article in Journal/Newspaper
author Sathish Kumar M1
Poobitha S 2
Ramajayan P 3
spellingShingle Sathish Kumar M1
Poobitha S 2
Ramajayan P 3
Canine Transmissible Venereal Tumor
author_facet Sathish Kumar M1
Poobitha S 2
Ramajayan P 3
author_sort Sathish Kumar M1
title Canine Transmissible Venereal Tumor
title_short Canine Transmissible Venereal Tumor
title_full Canine Transmissible Venereal Tumor
title_fullStr Canine Transmissible Venereal Tumor
title_full_unstemmed Canine Transmissible Venereal Tumor
title_sort canine transmissible venereal tumor
publisher Zenodo
publishDate 2022
url https://doi.org/10.5281/zenodo.7422158
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source The Science World a monthly e magazine, 2(12), 2070-2075, (2022-12-10)
op_relation https://zenodo.org/communities/thescienceworld
https://doi.org/10.5281/zenodo.7422157
https://doi.org/10.5281/zenodo.7422158
oai:zenodo.org:7422158
op_rights info:eu-repo/semantics/openAccess
Creative Commons Attribution 4.0 International
https://creativecommons.org/licenses/by/4.0/legalcode
op_doi https://doi.org/10.5281/zenodo.742215810.5281/zenodo.7422157
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