Immunofluorometric quantitation and histochemical localisation of kallikrein 6 protein in ovarian cancer tissue: a new independent unfavourable prognostic biomarker

被引:64
作者
Hoffman, BR
Katsaros, D
Scorilas, A
Diamandis, P
Fracchioli, S
de la Longrais, IAR
Colgan, T
Puopolo, M
Giardina, G
Massobrio, M
Diamandis, EP
机构
[1] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 1L5, Canada
[3] Univ Turin, Dept Gynecol, Gynecol Oncol Unit, I-10126 Turin, Italy
[4] Natl Ctr Sci Res Demokritos, IPC, Athens 15310, Greece
[5] St Anna Hosp, Dept Breast & Gynecol Oncol, I-10126 Turin, Italy
关键词
kallikrein; 6; prognosis; ovarian cancer; survival; biomarker;
D O I
10.1038/sj.bjc.6600533
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human kallikrein 6 protein is a newly discovered human kallikrein. We determined the amount of human kallikrein 6 in extracts of 182 ovarian tumours and correlated specific activity (ng hK6 mg(-1) total protein) with clinicopathological variables documented at the time of surgical excision and with outcome (progression free survival, overall survival) monitored over a median interval of 62 months. Thirty per cent of the tumours were positive for human kallikrein 6 (> 35 ng hK6 mg(-1) total protein). Human kallikrein 6-specific immunohistochemical staining of four ovarian tissues that included benign, borderline and malignant lesions indicated a cytoplasmic location of human kallikrein 6 in tumour cells of epithelial origin, although the intensity of staining was variable. Tumour human kallikrein 6 (ng hK6 mg(-1) total protein) was higher in late stage disease, serous histotype, residual tumour > 1 cm and suboptimal debulking (> 1 cm) (P < 0.05). Univariate analysis revealed that patients with tumour human kallikrein 6 positive specific activity were more likely to suffer progressive disease and to die (hazard ratio 1.71 (P = 0.015) and 1.88 (P = 0.022), respectively). Survival curves demonstrated the same (P = 0.013 and 0.019, respectively). Multivariate analysis revealed that human kallikrein 6 positivity was retained as an independent prognostic variable in several subgroups of patients, namely those with (low) grade I and 11 tumours (hazard ratio progression free survival 4.3 (P = 0.027) and overall survival 4.1 (P = 0.023)) and those with optimal debulking (hazard ratio progression free survival 3.8 (P = 0.019) and overall survival 5.6 (P = 0.011)). We conclude that tumour kallikrein 6 protein levels have utility as an independent adverse prognostic marker in a subgroup of ovarian cancer patients with otherwise apparently good prognosis. (C) 2002 Cancer Research UK.
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收藏
页码:763 / 771
页数:9
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