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Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?

Bibliographic Details
Main Author: Fêo,Haline B.
Publication Date: 2022
Other Authors: Flórez,Luis Mauricio M., Yamatogi,Ricardo S., Duzanski,Anderson P., Araújo Junior,João P., Oliveira,Rogerio A., Rocha,Noeme S.
Format: Article
Language: eng
Source: Pesquisa Veterinária Brasileira (Online)
Download full: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2022000100407
Summary: ABSTRACT: Canine transmissible venereal tumor (CTVT) is the oldest known somatic cell lineage. It is a transmissible cancer that propagates naturally in dogs and reportedly contains gene mutations. RASSF1 participates in DNA damage repair, and its downregulation, results in tumor progression. Hence, RASSF1 is a tumor suppressor gene. Its expression was quantified in tumors from seventeen animals and three cell cultures derived from tumors. In general, RASSF1 was underexpressed in 65%, and absent in 35% of tumor samples. Cells from tumor tissue cultures showed decreased expression of RASSF1 in 67% and elevated expression in 33% of samples tested. The tumor tissues showed significantly lower levels of RASSF1 expression compared to cultured cells. Previously we reported that both the tumor microenvironment and the host immune system appear to influence the tumorigenesis and stage of CTVT. This is the first article to demonstrate the expression of RASSF1 in CTVT. Decreased RASSF1 possibly helps tumor progression.
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spelling Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?DysregulationRASSF1tumorigenesiscanine transmissible venereal tumorCTVTABSTRACT: Canine transmissible venereal tumor (CTVT) is the oldest known somatic cell lineage. It is a transmissible cancer that propagates naturally in dogs and reportedly contains gene mutations. RASSF1 participates in DNA damage repair, and its downregulation, results in tumor progression. Hence, RASSF1 is a tumor suppressor gene. Its expression was quantified in tumors from seventeen animals and three cell cultures derived from tumors. In general, RASSF1 was underexpressed in 65%, and absent in 35% of tumor samples. Cells from tumor tissue cultures showed decreased expression of RASSF1 in 67% and elevated expression in 33% of samples tested. The tumor tissues showed significantly lower levels of RASSF1 expression compared to cultured cells. Previously we reported that both the tumor microenvironment and the host immune system appear to influence the tumorigenesis and stage of CTVT. This is the first article to demonstrate the expression of RASSF1 in CTVT. Decreased RASSF1 possibly helps tumor progression.Colégio Brasileiro de Patologia Animal - CBPA2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2022000100407Pesquisa Veterinária Brasileira v.42 2022reponame:Pesquisa Veterinária Brasileira (Online)instname:Colégio Brasileiro de Patologia Animal (CBPA)instacron:EMBRAPA10.1590/1678-5150-pvb-7082info:eu-repo/semantics/openAccessFêo,Haline B.Flórez,Luis Mauricio M.Yamatogi,Ricardo S.Duzanski,Anderson P.Araújo Junior,João P.Oliveira,Rogerio A.Rocha,Noeme S.eng2022-07-22T00:00:00Zoai:scielo:S0100-736X2022000100407Revistahttp://www.pvb.com.br/https://old.scielo.br/oai/scielo-oai.phpcolegio@cbpa.org.br||pvb@pvb.com.br0100-736X1678-5150opendoar:2022-07-22T00:00Pesquisa Veterinária Brasileira (Online) - Colégio Brasileiro de Patologia Animal (CBPA)false
dc.title.none.fl_str_mv Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
title Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
spellingShingle Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
Fêo,Haline B.
Dysregulation
RASSF1
tumorigenesis
canine transmissible venereal tumor
CTVT
title_short Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
title_full Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
title_fullStr Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
title_full_unstemmed Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
title_sort Could dysregulation of RASSF1 expression be a mechanism of tumorigenesis in CTVT?
author Fêo,Haline B.
author_facet Fêo,Haline B.
Flórez,Luis Mauricio M.
Yamatogi,Ricardo S.
Duzanski,Anderson P.
Araújo Junior,João P.
Oliveira,Rogerio A.
Rocha,Noeme S.
author_role author
author2 Flórez,Luis Mauricio M.
Yamatogi,Ricardo S.
Duzanski,Anderson P.
Araújo Junior,João P.
Oliveira,Rogerio A.
Rocha,Noeme S.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Fêo,Haline B.
Flórez,Luis Mauricio M.
Yamatogi,Ricardo S.
Duzanski,Anderson P.
Araújo Junior,João P.
Oliveira,Rogerio A.
Rocha,Noeme S.
dc.subject.por.fl_str_mv Dysregulation
RASSF1
tumorigenesis
canine transmissible venereal tumor
CTVT
topic Dysregulation
RASSF1
tumorigenesis
canine transmissible venereal tumor
CTVT
description ABSTRACT: Canine transmissible venereal tumor (CTVT) is the oldest known somatic cell lineage. It is a transmissible cancer that propagates naturally in dogs and reportedly contains gene mutations. RASSF1 participates in DNA damage repair, and its downregulation, results in tumor progression. Hence, RASSF1 is a tumor suppressor gene. Its expression was quantified in tumors from seventeen animals and three cell cultures derived from tumors. In general, RASSF1 was underexpressed in 65%, and absent in 35% of tumor samples. Cells from tumor tissue cultures showed decreased expression of RASSF1 in 67% and elevated expression in 33% of samples tested. The tumor tissues showed significantly lower levels of RASSF1 expression compared to cultured cells. Previously we reported that both the tumor microenvironment and the host immune system appear to influence the tumorigenesis and stage of CTVT. This is the first article to demonstrate the expression of RASSF1 in CTVT. Decreased RASSF1 possibly helps tumor progression.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2022000100407
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2022000100407
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-5150-pvb-7082
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Colégio Brasileiro de Patologia Animal - CBPA
publisher.none.fl_str_mv Colégio Brasileiro de Patologia Animal - CBPA
dc.source.none.fl_str_mv Pesquisa Veterinária Brasileira v.42 2022
reponame:Pesquisa Veterinária Brasileira (Online)
instname:Colégio Brasileiro de Patologia Animal (CBPA)
instacron:EMBRAPA
instname_str Colégio Brasileiro de Patologia Animal (CBPA)
instacron_str EMBRAPA
institution EMBRAPA
reponame_str Pesquisa Veterinária Brasileira (Online)
collection Pesquisa Veterinária Brasileira (Online)
repository.name.fl_str_mv Pesquisa Veterinária Brasileira (Online) - Colégio Brasileiro de Patologia Animal (CBPA)
repository.mail.fl_str_mv colegio@cbpa.org.br||pvb@pvb.com.br
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