Author/Authors :
Nishikawa، نويسنده , , Kazuhiro and Satoh، نويسنده , , Haruna and Hirai، نويسنده , , Ayako and Suzuzki، نويسنده , , Kazuyuki and Asano، نويسنده , , Ryuji and Kumadaki، نويسنده , , Itsumaro and Hagiwara، نويسنده , , Kiyokazu and Yano، نويسنده , , Tomohiro، نويسنده ,
Abstract :
The overexpression of HER-2 receptor contributes to malignant transformation of breast cancer cells. We have reported that α-tocopheryloxybutyric acid (TE), non-antioxidative vitamin E ether derivative inhibits the activation of HER-2 receptor. The present study was undertaken to estimate if TE could act as a useful anti-cancer agent against a breast cancer cell overexpressing HER-2 receptor (MDA-MB-453 cell line) in combination with a conventional chemotherapy agent, adriamycin (ADR). TE enhanced cytotoxic effect of ADR against the human breast cancer cell at low doses less than IC50. The enhancing effect was mainly dependent on the elevation of necrotic-like cell death but not apoptotic cell death. In conjugation with this event, the inactivation of HER-2 receptor in the breast cancer cell was caused by the combination of TE with ADR. These results suggest that TE enhances necrotic-like cell death in the breast cancer cells and that the cell death relates to the inactivation of HER-2 receptor in the breast cancer cells.
Keywords :
adriamycin , breast cancer , Necrotic-like cell death , HER-2 receptor , Vitamin E ether derivative