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Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property

INTRODUCTION: Canine transmissible venereal tumour (CTVT) is a sexually transmitted tumour affecting dogs worldwide, imposing a financial burden on dog owners. A stable culture cell line in continuous passages for >18 months has only been achieved once. The present study investigated a stable CTV...

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Autores principales: Zayas, Yareellys Ramos, Molina, Moisés Armides Franco, Guerra, Reyes Tamez, Padilla, Cristina Rodríguez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598177/
https://www.ncbi.nlm.nih.gov/pubmed/31276062
http://dx.doi.org/10.2478/jvetres-2019-0024
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author Zayas, Yareellys Ramos
Molina, Moisés Armides Franco
Guerra, Reyes Tamez
Padilla, Cristina Rodríguez
author_facet Zayas, Yareellys Ramos
Molina, Moisés Armides Franco
Guerra, Reyes Tamez
Padilla, Cristina Rodríguez
author_sort Zayas, Yareellys Ramos
collection PubMed
description INTRODUCTION: Canine transmissible venereal tumour (CTVT) is a sexually transmitted tumour affecting dogs worldwide, imposing a financial burden on dog owners. A stable culture cell line in continuous passages for >18 months has only been achieved once. The present study investigated a stable CTVT cell line isolated from a bitch and its potential as a vaccine. MATERIAL AND METHODS: A biopsy from a 2-year-old mongrel bitch with CTVT was obtained for histopathological confirmation and isolation of tumour cells. The isolated cells were cultured to passage 55 and characterised by flow cytometry, with karyotyping by GTG-banding and by PCR detection of myc S-2 and LINE AS1. The isolated CTVT cell line was also used as a preventive vaccine in a canine model. RESULTS: Histopathological analysis of the isolated tumour cells revealed typical CTVT characteristics. Constant proliferation and stable morphological characteristics were observed during culture. Phenotypic analysis determined the expression of HLA-DR(+), CD5.1(+), CD14(+), CD45(+), CD83(+), CD163(+), and Ly-6G-Ly-6C(+). GTG-banding revealed a mean of 57 chromosomes in the karyotype with several complex chromosomal rearrangements. LINE-c-myc insertion in the isolated CTVT cell line at 550 bp was not detected. However, a 340-bp band was amplified. Isolated CTVT cell line inoculation at a concentration of 1×10(8) did not induce tumour growth in bitches, nor did a challenge with primary CTVT cells. CONCLUSION: The present study successfully identified and isolated a stable CTVT cell line that may be useful in CTVT prevention.
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spelling pubmed-65981772019-07-02 Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property Zayas, Yareellys Ramos Molina, Moisés Armides Franco Guerra, Reyes Tamez Padilla, Cristina Rodríguez J Vet Res Research Article INTRODUCTION: Canine transmissible venereal tumour (CTVT) is a sexually transmitted tumour affecting dogs worldwide, imposing a financial burden on dog owners. A stable culture cell line in continuous passages for >18 months has only been achieved once. The present study investigated a stable CTVT cell line isolated from a bitch and its potential as a vaccine. MATERIAL AND METHODS: A biopsy from a 2-year-old mongrel bitch with CTVT was obtained for histopathological confirmation and isolation of tumour cells. The isolated cells were cultured to passage 55 and characterised by flow cytometry, with karyotyping by GTG-banding and by PCR detection of myc S-2 and LINE AS1. The isolated CTVT cell line was also used as a preventive vaccine in a canine model. RESULTS: Histopathological analysis of the isolated tumour cells revealed typical CTVT characteristics. Constant proliferation and stable morphological characteristics were observed during culture. Phenotypic analysis determined the expression of HLA-DR(+), CD5.1(+), CD14(+), CD45(+), CD83(+), CD163(+), and Ly-6G-Ly-6C(+). GTG-banding revealed a mean of 57 chromosomes in the karyotype with several complex chromosomal rearrangements. LINE-c-myc insertion in the isolated CTVT cell line at 550 bp was not detected. However, a 340-bp band was amplified. Isolated CTVT cell line inoculation at a concentration of 1×10(8) did not induce tumour growth in bitches, nor did a challenge with primary CTVT cells. CONCLUSION: The present study successfully identified and isolated a stable CTVT cell line that may be useful in CTVT prevention. Sciendo 2019-06-12 /pmc/articles/PMC6598177/ /pubmed/31276062 http://dx.doi.org/10.2478/jvetres-2019-0024 Text en © 2019 Y.R. Zayas et al. published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Research Article
Zayas, Yareellys Ramos
Molina, Moisés Armides Franco
Guerra, Reyes Tamez
Padilla, Cristina Rodríguez
Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property
title Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property
title_full Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property
title_fullStr Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property
title_full_unstemmed Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property
title_short Evaluation of a Canine Transmissible Venereal Tumour Cell Line with Tumour Immunity Capacity but Without Tumorigenic Property
title_sort evaluation of a canine transmissible venereal tumour cell line with tumour immunity capacity but without tumorigenic property
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598177/
https://www.ncbi.nlm.nih.gov/pubmed/31276062
http://dx.doi.org/10.2478/jvetres-2019-0024
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