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C(3)1-TAg in C57BL/6 J background as a model to study mammary tumor development.
Sena, Isadora F G; Rocha, Beatriz G S; Picoli, Caroline C; Santos, Gabryella S P; Costa, Alinne C; Gonçalves, Bryan O P; Garcia, Ana Paula V; Soltani-Asl, Maryam; Coimbra-Campos, Leda M C; Silva, Walison N; Costa, Pedro A C; Pinto, Mauro C X; Amorim, Jaime H; Azevedo, Vasco A C; Resende, Rodrigo R; Heller, Debora; Cassali, Geovanni D; Mintz, Akiva; Birbrair, Alexander.
Afiliação
  • Sena IFG; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Rocha BGS; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Picoli CC; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Santos GSP; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Costa AC; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Gonçalves BOP; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Garcia APV; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Soltani-Asl M; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Coimbra-Campos LMC; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Silva WN; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Costa PAC; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Pinto MCX; Laboratory of Neuropharmacology and Neurochemistry, Institute of Biological Sciences, Federal University of Goiás, Goiânia, GO, Brazil.
  • Amorim JH; Center of Biological Sciences and Health, Federal University of West Bahia, Barreiras, BA, Brazil.
  • Azevedo VAC; Cellular and Molecular Genetics Laboratory, Department of Genetics, Ecology and Evolution, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Resende RR; Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Heller D; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Cassali GD; Cruzeiro Do Sul University, São Paulo, Brazil.
  • Mintz A; Department of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
  • Birbrair A; Department of Radiology, Columbia University Medical Center, New York, NY, USA.
Histochem Cell Biol ; 156(2): 165-182, 2021 Aug.
Article em En | MEDLINE | ID: mdl-34003355
ABSTRACT
Diagnosis and prognosis of breast cancer is based on disease staging identified through histopathological and molecular biology techniques. Animal models are used to gain mechanistic insights into the development of breast cancer. C(3)1-TAg is a genetically engineered mouse model that develops mammary cancer. However, carcinogenesis caused by this transgene was characterized in the Friend Virus B (FVB) background. As most genetic studies are done in mice with C57BL/6 J background, we aimed to define the histological alterations in C3(1)-TAg C57BL/6 J animals. Our results showed that C3(1)-TAg animals with C57BL/6 J background develop solid-basaloid adenoid cystic carcinomas with increased fibrosis, decreased area of adipocytes, and a high proliferative index, which are triple-negative for progesterone, estrogen, and human epidermal growth factor receptor 2 (HER2) receptors. Our results also revealed that tumor development is slower in the C57BL/6 J background when compared with the FVB strain, providing a better model to study the different stages in breast cancer progression.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Carcinoma Adenoide Cístico / Modelos Genéticos / Antígenos Virais de Tumores Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Carcinoma Adenoide Cístico / Modelos Genéticos / Antígenos Virais de Tumores Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article