Cleaved caspase-3 and nuclear factor-κB p65 are prognostic factors in metastatic serous ovarian carcinoma

被引:58
作者
Kleinberg, Lilach [1 ]
Dong, Hiep Phuc [1 ]
Holth, Arild [1 ]
Risberg, Bjoern [1 ]
Trope, Claes G. [2 ]
Nesland, Jahn M. [1 ]
Florenes, Vivi Ann [1 ]
Davidson, Ben [1 ]
机构
[1] Univ Oslo, Rikshosp, Norwegian Radium Hosp, Med Ctr,Div Pathol, N-0310 Oslo, Norway
[2] Univ Oslo, Rikshosp, Norwegian Radium Hosp, Med Ctr,Div Gynecol, N-0310 Oslo, Norway
关键词
NF-kappa B; Caspase; Apoptosis; Chemotherapy; Ovarian carcinoma; Serous effusions; Survival; CHEMOTHERAPY-INDUCED APOPTOSIS; CANCER-CELLS; IN-VITRO; INHIBITORY PROTEIN; EPITHELIAL-CELLS; EXPRESSION; ACTIVATION; RESISTANCE; PATHWAYS; DEATH;
D O I
10.1016/j.humpath.2008.10.019
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Tumor progression and treatment failure: in ovarian carcinoma are frequently associated with metastasis to effusions. The present study analyzed the expression and clinical role of nuclear factor-kappa B p65, nuclear factor-kappa B inhibitor alpha, and parameters of apoptosis in serous carcinoma. Cleaved caspase-3 and caspase-8 levels and deoxyuridine triphosphate incorporation were measured in 65 effusions using flow cytometry. Effusions (n = 209) and corresponding primary carcinomas and solid metastases (n = 114) were immunohistochemically analyzed for nuclear factor-kappa B p65 and nuclear factor-kappa B inhibitor a expression. Effusions (n = 75) were further analyzed for nuclear factor-kappa B phospho-p65 (Ser536) levels using immunoblotting. Results were analyzed for association with anatomic site, clinicopathologic parameters, and survival. Caspase cleavage and deoxyuridine triphosphate incorporation were limited to less than 10% of cells in most effusions. Nuclear factor-kappa B p65 expression was frequently detected at all anatomic sites, with less frequent cytoplasmic nuclear factor-kappa B p65 and nuclear factor-kappa B inhibitor a expressions. Immunoblotting showed nuclear factor-kappa B p65 phosphorylation in 72 (96%) of 75 effusions. Higher than median cleaved caspase-3 levels correlated with improved overall and progression-free survival in univariate analysis of all patients (P = .024 and P = .046, respectively) and of those with postchemotherapy effusions (P = .042 and P = .036, respectively). Cleaved caspase-3 expression was an independent predictor of longer progression-free survival for patients with postchemotherapy effusions (P = .029). Nuclear factor-kappa B p65 expression correlated with poor progression-free survival for all patients (P = .048) and for those with postchemotherapy effusions (P = .025). Ovarian carcinoma cells in effusions undergo little apoptosis, but high levels of cleaved caspase-3 are associated with improved survival. Nuclear factor-kappa B p65 is frequently expressed in advanced-stage serous ovarian carcinoma, and its nuclear localization is associated with poor progression-free survival. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:795 / 806
页数:12
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