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Black tea protects immunocytes from tumor-induced apoptosis by changing Bcl-2/Bax ratio.
Bhattacharyya, Arindam; Mandal, Debaprasad; Lahiry, Lakshmishri; Sa, Gaurisankar; Das, Tanya.
Afiliação
  • Bhattacharyya A; Bose Institute, P-1/12 CIT Scheme VII M, Kolkata 700 054, India.
Cancer Lett ; 209(2): 147-54, 2004 Jun 25.
Article em En | MEDLINE | ID: mdl-15159016
It is known that cancer is associated with altered immune function. We demonstrated earlier that black tea inhibits tumor growth in a dose-dependent manner. Here, we report that apoptosis was the cause of immunocyte death in Ehrlich's ascites carcinoma (EAC)-bearing mice and anti-tumor dose of black tea restored EAC-induced immunosuppression by inhibiting apoptosis. A search for the molecular mechanism revealed that EAC burden increased the expression of the pro-apoptotic proteins p53 and Bax in splenic lymphocytes although did not change the level of pro-proliferative protein Bcl-2. Interestingly, anti-tumor dose of black tea down-regulated p53, decreased Bax while augmenting Bcl-2 in these cells. As a result, Bcl-2/Bax ratio was increased and the immunocytes were protected from tumor-induced apoptosis. Thus, unlike many other anti-cancer agents, black tea is not only devoid of immunosuppressive effect but also acts as immuno-restorer in tumor-bearing host. These results, thus, raise the possibility of inclusion of black tea in successful therapeutic regimen against cancer.
Assuntos
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Base de dados: MEDLINE Assunto principal: Chá / Carcinoma de Ehrlich / Linfócitos / Proteínas Proto-Oncogênicas / Apoptose / Proteínas Proto-Oncogênicas c-bcl-2 Limite: Animals Idioma: En Revista: Cancer Lett Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Índia
Buscar no Google
Base de dados: MEDLINE Assunto principal: Chá / Carcinoma de Ehrlich / Linfócitos / Proteínas Proto-Oncogênicas / Apoptose / Proteínas Proto-Oncogênicas c-bcl-2 Limite: Animals Idioma: En Revista: Cancer Lett Ano de publicação: 2004 Tipo de documento: Article País de afiliação: Índia