The prognostic significance of COX-2 and survivin expression in ovarian cancer

被引:47
作者
Athanassiadou, Pauline [1 ]
Grapsa, Dimitra [1 ]
Athanassiades, Peter [2 ]
Gonidi, Maria [1 ]
Athanassiadou, Anna-Maria [1 ]
Tsipis, Angelos [2 ]
Patsouris, Efstratios [1 ]
机构
[1] Univ Athens, Sch Med, Cytol Dept, Pathol Lab, GR-11527 Athens, Greece
[2] Univ Athens, Sch Med, Alexandra Hosp, Dept Clin Therapeut, GR-11527 Athens, Greece
关键词
ovarian cancer; COX-2; survivin; prognosis; immunocytochemistry;
D O I
10.1016/j.prp.2007.11.004
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
We investigated the prognostic significance of cyclooxygenase-2 (COX-2) and survivin in ovarian carcinoma. Imprint smears were obtained from 100 ovarian carcinoma specimens and were studied immunocytochemically for the expression of COX-2 and survivin. The results were correlated with several clinicopathological parameters, including 5-year survival. Increased COX-2 staining pattern correlated with a non-mucinous histological type (p = 0.008), increased stage (p < 0.0001), high histological grade (p < 0.0001), and reduced survival rates (p < 0.00001). Survivin expression was strongly associated with increased stage (p < 0.0001), increased histological grade (p < 0.0001), and reduced survival (p < 0.00001). Elevated survivin expression also correlated significantly with pre-menopausal status (p = 0.033). In addition, COX-2 and survivin staining patterns correlated strongly with one another (p < 0.0001). However, on multivariate analysis, an independent prognostic value was found only for tumor stage and grade. The findings of our study indicate that the increased expression of COX-2 and survivin in ovarian cancer is associated with one another and with several adverse clinicopathologic parameters, including reduced survival, thus suggesting a role of these molecules in disease progression. Further investigations of the exact prognostic and therapeutic implications of COX-2 and survivin expression are strongly warranted. (c) 2007 Elsevier GmbH. All rights reserved.
引用
收藏
页码:241 / 249
页数:9
相关论文
共 77 条
[1]
Comparison of frozen section and touch imprint cytology for evaluation of sentinel lymph node metastasis in breast cancer [J].
Aihara, T ;
Munakata, S ;
Morino, H ;
Takatsuka, Y .
ANNALS OF SURGICAL ONCOLOGY, 2004, 11 (08) :747-750
[2]
Touch imprint cytology and immunohistochemistry for the assessment of sentinel lymph nodes in patients with breast cancer [J].
Aihara, T ;
Munakata, S ;
Morino, H ;
Takatsuka, Y .
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2003, 29 (10) :845-848
[3]
The effect of cyclooxygenase-2 expression on tumor vascularity in advanced stage ovarian serous carcinoma [J].
Ali-Fehmi, R ;
Che, MX ;
Khalifeh, I ;
Malone, JM ;
Morris, R ;
Lawrence, WD ;
Munkarah, AR .
CANCER, 2003, 98 (07) :1423-1429
[4]
A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[5]
[Anonymous], KOSS DIAGNOSTIC CYTO
[6]
Contemporary issues in women's health [J].
Arulkumaran, S ;
Johnson, TRB .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2003, 83 (01) :1-3
[7]
Expression of p120, Ki-67 and PCNA as proliferation biomarkers in imprint smears of prostate carcinoma and their prognostic value [J].
Bantis, A ;
Giannopoulos, A ;
Gonidi, M ;
Liossi, A ;
Aggelonidou, E ;
Petrakakou, E ;
Athanassiades, P ;
Athanassiadou, P .
CYTOPATHOLOGY, 2004, 15 (01) :25-31
[8]
Feasibility of performing chemoprevention trials in women at elevated risk of ovarian carcinoma: Initial examination of celecoxib as a chemopreventive agent [J].
Barnes, MN ;
Chhieng, DF ;
Dreher, M ;
Jones, JL ;
Grizzle, WE ;
Jones, L ;
Talley, L ;
Partridge, EE .
GYNECOLOGIC ONCOLOGY, 2005, 98 (03) :376-382
[9]
Ovulation induction and cancer risk [J].
Brinton, LA ;
Moghissi, KS ;
Scoccia, B ;
Westhoff, CL ;
Lamb, EJ .
FERTILITY AND STERILITY, 2005, 83 (02) :261-274
[10]
THE ROLE OF CYTOKINES IN THE PRODUCTION OF PROSTACYCLIN AND THROMBOXANE IN HUMAN MONONUCLEAR-CELLS [J].
CHEN, G ;
WILSON, R ;
MCKILLOP, JH ;
WALKER, JJ .
IMMUNOLOGICAL INVESTIGATIONS, 1994, 23 (4-5) :269-279