Incidence, mechanism and prognostic value of activated AKT in pancreas cancer

被引:217
作者
Schlieman, MG
Fahy, BN
Ramsamooj, R
Beckett, L
Bold, RJ
机构
[1] Univ Calif Davis, Med Ctr, Dept Surg, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Med Ctr, Dept Pathol, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Med Ctr, Dept Epidemiol & Prevent Med, Sacramento, CA 95817 USA
关键词
pancreatic cancer; AKT; HER-2/neu;
D O I
10.1038/sj.bjc.6601396
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
When activated, the serine/threonine kinase AKT mediates an antiapoptotic signal implicated in chemoresistance of various cancers. The mechanism(s) of AKT activation are unknown, though overexpression of HER-2/neu has been implicated in breast cancer, Therefore, we determined the incidence of activated AKT in human pancreatic cancer, whether HER-2/neu is involved in AKT activation, and if AKT activation is associated with biologic behaviour. HER-2/neu expression and AKT activation were examined in seven pancreatic cancer cell lines by Western blotting. The in vitro effect of HER-2/neu inhibition on AKT activation was similarly determined. Finally, 78 pancreatic cancer specimens were examined for AKT activation and HER-2/neu overexpression, and correlated with the clinical prognostic variable of histologic grade. HER-2/neu was overexpressed in two of seven cell lines; these two cell lines demonstrated the highest level of AKT activation. Inhibition of HER-2/neu reduced AKT activation in vitro. AKT was activated in 46 out of 78 (59%) of the pancreatic cancers; HER-2/neu overexpression correlated with AKT activation (P = 0.015). Furthermore, AKT activation was correlated with higher histologic tumour grade (P = 0.047). Thus, it is concluded that AKT is frequently activated in pancreatic cancer; this antiapoptotic signal may be mediated by HER-2/neu overexpression. AKT activation is associated with tumour grade, an important prognostic factor.
引用
收藏
页码:2110 / 2115
页数:6
相关论文
共 40 条
[21]   Differential mechanisms of constitutive Akt/PKB activation and its influence on gene expression in pancreatic cancer cells [J].
Matsumoto, J ;
Kaneda, M ;
Tada, M ;
Hamada, J ;
Okushiba, S ;
Kondo, S ;
Katoh, H ;
Moriuchi, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 2002, 93 (12) :1317-1326
[22]  
Ng SSW, 2000, CANCER RES, V60, P5451
[23]  
Ng SSW, 2001, CLIN CANCER RES, V7, P3269
[24]   Activation of AKT/PKB in breast cancer predicts a worse outcome among endocrine treated patients [J].
Pérez-Tenorio, G ;
Stål, O .
BRITISH JOURNAL OF CANCER, 2002, 86 (04) :540-545
[25]   Pancreatic cancer cell proliferation is phosphatidylinositol 3-kinase dependent [J].
Perugini, RA ;
McDade, TP ;
Vittimberga, FJ ;
Callery, MP .
JOURNAL OF SURGICAL RESEARCH, 2000, 90 (01) :39-44
[26]  
Ruggeri BA, 1998, MOL CARCINOGEN, V21, P81, DOI 10.1002/(SICI)1098-2744(199802)21:2<81::AID-MC1>3.0.CO
[27]  
2-R
[28]   Transforming growth factor-β2 is a transcriptional target for Akt/protein kinase B via forkhead transcription factor [J].
Samatar, AA ;
Wang, LQ ;
Mirza, A ;
Koseoglu, S ;
Liu, SX ;
Kumar, CC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (31) :28118-28126
[29]  
Sano T, 1999, CANCER RES, V59, P1820
[30]  
Takahashi T, 1997, HEPATO-GASTROENTEROL, V44, P1463