Induction of apoptosis in a human breast cancer cell overexpressing ErbB-2 receptor by α-tocopheryloxybutyric acid

被引:24
作者
Akazawa, A
Nishikawa, K
Suzuki, K
Asano, R
Kumadaki, I
Satoh, H
Hagiwara, K
Shin, SJ
Yano, T
机构
[1] Natl Inst Hlth & Nutr, Dept Food Sci Res Hlth, Shinjuku Ku, Tokyo 1628636, Japan
[2] Nihon Univ, Coll Bioresource Sci, Dept Vet Pharmacol, Kanagawa 2528510, Japan
[3] Setsunan Univ, Fac Pharmaceut Sci, Osaka 5730101, Japan
关键词
alpha-tocopheryloxybutyric acid; apoptosis; breast cancer cell;
D O I
10.1254/jjp.89.417
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The overexpression of ErbB-2 receptor relates to malignant transformation of breast cancer. The present study was carried out to establish the usefulness of a-tocopheryloxybutyric acid (TE) as a chemotherapeutic agent for human breast cancer. TE caused induction of apoptosis in MDA-MB-453 cells overexpressing the ErbB-2 receptor. TE reduced levels of activated ErbB-2 receptor and Akt. In contrast, TE induced the activation of p38, and SB203580, a specific inhibitor for p38, attenuated the TE-induced apoptosis. These data indicate that simultaneous occurrences of Akt inhibition and p38 activation by TE result in the cell death.
引用
收藏
页码:417 / 421
页数:5
相关论文
共 17 条
[1]   The activation of p38 and apoptosis by the inhibition of ERK is antagonized by the phosphoinositide S-kinase/Akt pathway [J].
Berra, E ;
Diaz-Meco, MT ;
Moscat, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (17) :10792-10797
[2]   RRR-alpha-tocopheryl succinate enhances TGF-beta(1), -beta(2), and -beta(3) and TGF-beta R-II expression by human MDA-MB-435 breast cancer cells [J].
Charpentier, A ;
SimmonsMenchaca, M ;
Yu, WP ;
Zhao, BH ;
Qian, M ;
Heim, K ;
Sanders, BG ;
Kline, K .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1996, 26 (02) :237-250
[3]  
FARRIS MW, 1994, CANCER RES, V54, P3346
[4]   DNA damaging agents induce expression of Fas ligand and subsequent apoptosis in T lymphocytes via the activation of NF-KB and AP-1 [J].
Kasibhatla, S ;
Brunner, T ;
Genestier, L ;
Echeverri, F ;
Mahboubi, A ;
Green, DR .
MOLECULAR CELL, 1998, 1 (04) :543-551
[5]  
Kelloff G J, 1994, J Cell Biochem Suppl, V20, P282
[6]  
KERN JA, 1990, CANCER RES, V50, P5184
[7]  
Ménard S, 2000, J CELL PHYSIOL, V182, P150, DOI 10.1002/(SICI)1097-4652(200002)182:2<150::AID-JCP3>3.0.CO
[8]  
2-E
[9]   Akt, MAPK (Erk1/2), and p38 act in concert to promote apoptosis in response to ErbB receptor family inhibition [J].
Nelson, JM ;
Fry, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (18) :14842-14847
[10]   HER2/neu antisense targeting of human breast carcinoma [J].
Roh, H ;
Pippin, JA ;
Green, DW ;
Boswell, CB ;
Hirose, CT ;
Mokadam, N ;
Drebin, JA .
ONCOGENE, 2000, 19 (53) :6138-6143