The ErbB signalling pathway: protein expression and prognostic value in epithelial ovarian cancer

被引:71
作者
de Graeff, P. [1 ]
Crijns, A. P. G. [1 ]
ten Hoor, K. A. [1 ]
Klip, H. G. [1 ]
Hollema, H. [2 ]
Oien, K. [3 ]
Bartlett, J. M. [4 ]
Wisman, G. B. A. [1 ]
de Bock, G. H. [5 ]
de Vries, E. G. E. [6 ]
de Jong, S. [6 ]
van der Zee, A. G. J. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Gynecol Oncol, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol, NL-9713 GZ Groningen, Netherlands
[3] Ctr Oncol & Appl Pharmacol, Canc Res UK Beatson Labs, Glasgow G61 1BD, Lanark, Scotland
[4] Univ Edinburgh, Western Gen Hosp, Edinburgh Canc Res Ctr, Endocrine Canc Grp, Edinburgh EH4 2XR, Midlothian, Scotland
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol & Stat, NL-9713 GZ Groningen, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Med Oncol, NL-9713 GZ Groningen, Netherlands
关键词
ovarian cancer; prognosis; EGFR; HER-2/neu; PTEN; EGFRvIII;
D O I
10.1038/sj.bjc.6604471
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ovarian cancer is the most frequent cause of death from gynaecological cancer in the Western world. Current prognostic factors do not allow reliable prediction of response to chemotherapy and survival for individual ovarian cancer patients. Epidermal growth factor receptor (EGFR) and HER-2/neu are frequently expressed in ovarian cancer but their prognostic value remains unclear. In this study, we investigated the expression and prognostic value of EGFR, EGFR variant III (EGFRvIII), HER-2/neu and important downstream signalling components in a large series of epithelial ovarian cancer patients. Immunohistochemical staining of EGFR, pEGFR, EGFRvIII, Her-2/neu, PTEN (phosphatase and tensin homologue deleted on chromosome 10), total and phosphorylated AKT (pAKT) and phosphorylated ERK (pERK) was performed in 232 primary tumours using the tissue microarray platform and related to clinicopathological characteristics and survival. In addition, EGFRvIII expression was determined in 45 tumours by RT-PCR. Our results show that negative PTEN immunostaining was associated with stage I/II disease (P = 0.006), non-serous tumour type (P = 0.042) and in multivariate analysis with a longer progression-free survival (P = 0.015). Negative PTEN staining also predicted improved progression-free survival in patients with grade III or undifferentiated serous carcinomas (P = 0.011). Positive pAKT staining was associated with advanced-stage disease (P = 0.006). Other proteins were expressed only at low levels, and were not associated with any clinicopathological parameter or survival. None of the tumours were positive for EGFRvIII. In conclusion, our results indicate that tumours showing negative PTEN staining could represent a subgroup of ovarian carcinomas with a relatively favourable prognosis.
引用
收藏
页码:341 / 349
页数:9
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