Sabiia Seb
PortuguêsEspañolEnglish
Embrapa
        Busca avançada

Botão Atualizar


Botão Atualizar

Registro completo
Provedor de dados:  OAK
País:  Japan
Título:  Methylcholanthrene自家誘発腫瘍担癌ラットに対するトキソプラズマ溶解抗原の抗腫瘍効果
Antitumor Activity of Toxoplasma Lysate Antigen against Methylcholanthrene-Induced Tumor-Bearing Rats
Autores:  MIYAHARA, Kazuro
YOKOO, Naoya
SAKURAI, Haruhisa
IGARASHI, Ikuo
SAKATA, Yu
YOSHIDA, Yutaka
SAITO, Atsushi
HIROSE, Tsuneo
SUZUKI, Naoyoshi
宮原, 和郎
五十嵐, 郁男
Data:  1992
Ano:  1992
Palavras-chave:  Antitumor activity
Methylcholanthrene-autoinduced tumor
Rat
Thy-1 positive granular cell
Toxoplasma lysate antigen
Resumo:  Growth of the tumor autoinduced by 20-methylcholanthrene (MC) in rats was inhibited after administration of Toxoplasma lysate antigen (TLA). The antitumor activity of TLA was most obvious in the early stage of tumoral growth. When TLA was administered to rats before the appearance of tumor, tumor formation was delayed slightly. Histopathological studies revealed dense growths of spindle tumor cells in untreated control rat, while enlarged central necrosis with the infiltration of lymphocytes and neutrophils was apparent in TLA-treated rats. According to the immunohistological examination of tumor tissue with anti-Thy-1 antibody, the rats treated with TLA showed large Thy-1 positive granular cells, whereas the untreated rats indicated only a few small Thy-1 positive cells. These observations indicate that TLA is a useful modifier of biological responses to MC-induced tumors.

https://www.jstage.jst.go.jp/article/jvms1991/54/2/54_2_221/_article
Idioma:  Inglês
Identificador:  http://ir.obihiro.ac.jp/dspace/handle/10322/4064
Editor:  日本獣医学会
Direitos:  日本獣医学会
Fechar
 

Empresa Brasileira de Pesquisa Agropecuária - Embrapa
Todos os direitos reservados, conforme Lei n° 9.610
Política de Privacidade
Área restrita

Embrapa
Parque Estação Biológica - PqEB s/n°
Brasília, DF - Brasil - CEP 70770-901
Fone: (61) 3448-4433 - Fax: (61) 3448-4890 / 3448-4891 SAC: https://www.embrapa.br/fale-conosco

Valid HTML 4.01 Transitional