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Anti-Her-2/neu antibody induces apoptosis in Her-2/neu overexpressing breast cancer cells independently from p53 status.
Brodowicz, T; Kandioler, D; Tomek, S; Ludwig, C; Rudas, M; Kunstfeld, R; Koestler, W; Hejna, M; Budinsky, A; Wiltschke, C; Zielinski, C C.
Afiliación
  • Brodowicz T; Clinical Division of Oncology, University Hospital, Vienna, Austria.
Br J Cancer ; 85(11): 1764-70, 2001 Nov 30.
Article en En | MEDLINE | ID: mdl-11742500
ABSTRACT
Anti-Her-2/neu antibody is known to induce apoptosis in HER-2/neu overexpressing breast cancer cells. However, exact regulatory mechanisms mediating and controlling this phenomenon are still unknown. In the present study, we have investigated the effect of anti-Her-2/neu antibody on apoptosis of HER-2/neu overexpressing human breast cancer cell lines SK-BR-3, HTB-24, HTB-25, HTB-27, HTB-128, HTB-130 and HTB-131 in relation to p53 genotype and bcl-2 status. SK-BR-3, HTB-24, HTB-128 and HTB-130 cells exhibited mutant p53, whereas wild type p53 was found in HTB-25, HTB-27 and HTB-131 cells. All seven cell lines weakly expressed bcl-2 protein (10-20%). Anti-Her-2/neu antibody, irrespective of p53 and bcl-2 status, induced apoptosis in all 7 cell lines dose- and time-dependently and correlated with Her-2/neu overexpression. In addition, incubation of cell lines with anti-Her-2/neu antibody did not alter p53 or bcl-2 expression. Anti-HER-2/neu antibody did not induce apoptosis in HER-2/neu negative HBL-100 and HTB-132 cell lines. Our results indicate that within the panel of tested breast cancer cell lines, anti-Her-2/neu antibody-induced apoptosis was independent from the presence of intact p53.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Apoptosis / Receptor ErbB-2 / Anticuerpos Monoclonales Límite: Humans Idioma: En Año: 2001 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Apoptosis / Receptor ErbB-2 / Anticuerpos Monoclonales Límite: Humans Idioma: En Año: 2001 Tipo del documento: Article