Cyclooxygenase-2 expression in cervical cancer

被引:4
作者
Mandic, Aljosa [1 ]
Usaj-Knezevic, Slavica [1 ]
Kapicl, Tatjana Ivkovic [1 ]
Nincic, Dejan [1 ]
Malenkovic, Goran [1 ]
机构
[1] Oncol Inst Vojvodina, Novi Sad, Serbia
关键词
uterine cervical neoplasms; prostaglandin-endoperoxide synthases; immunohistochemistry; gene expression; sensitivity and specificity; TRANSITIONAL-CELL CARCINOMA; INDEPENDENT PROGNOSTIC-FACTOR; COX-2; EXPRESSION; INTRAEPITHELIAL NEOPLASIA; ENDOMETRIAL CARCINOMA; IN-SITU; OVEREXPRESSION; LESIONS; ADENOCARCINOMA; ANGIOGENESIS;
D O I
10.2298/VSP1411997M
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aim. Cyclooxygenase (COX) or prostaglandin H2 synthase is the first enzyme that catalyzes the first two steps in the biosynthesis of prostaglandins from arachidonic acid. The aim of the study was to determine the expression level of COX-2 in patients with cervical cancer and compare it with that in the control group with no cervical pathology. Methods. The study included 76 patients divided into two groups: the control group 30 patients without histopathological changes and the group A 46 patients with cervical cancer, FIGO stage Histopathological and immunohistochemical analyses were performed in these two groups of patients. Results. In the control group, the expression of COX-2 was not confirmed compared to the group A of 26 (56.52%) patients. The expression of COX-2 showed a statistically significant difference in the presence of lymphocytic stromal infiltration (p = 0.0053). The expression of COX-2 was more pronounced in the stromal tissue without lymphocytic infiltration (80% vs 20%). Conclusion. A higher expression of COX-2 in cervical carcinoma without stromal lymphocytic infiltration suggests a possible paradoxical effect of COX-2 in immunosuppression. Frequent COX-2 expression in the subgroup with poor prognostic histological parameters in the group A indicates the importance of COX-2 expression in the carcinogenesis of cervical cancer.
引用
收藏
页码:997 / 1005
页数:9
相关论文
共 48 条
[1]  
[Anonymous], 2010, GLOBOCAN 2008 V2 0 C
[2]   Survivin expression in in situ and invasive breast cancer relates to COX-2 expression and DCIS recurrence [J].
Barnes, N ;
Haywood, P ;
Flint, P ;
Knox, WF ;
Bundred, NJ .
BRITISH JOURNAL OF CANCER, 2006, 94 (02) :253-258
[3]   Intracellular unesterified arachidonic acid signals apoptosis [J].
Cao, Y ;
Pearman, AT ;
Zimmerman, GA ;
McIntyre, TM ;
Prescott, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (21) :11280-11285
[4]   Cyclooxygenase-2 expression is higher in ovarian cancer tissue adjacent to endometriosis than in ovarian cancer without comorbid endometriosis [J].
Chou, YC ;
Chen, YJ ;
Lai, CR ;
Wang, PH ;
Hsin-Chan ;
Yuan, CC .
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2006, 124 (01) :101-105
[5]  
Curado MP., 2007, CANC INCIDENCE 5 CON
[6]   The expression of cyclooxygenase-2, VEGF and PGs in CIN and cervical carcinoma [J].
Dai, YM ;
Zhang, XD ;
Peng, YH ;
Wang, ZR .
GYNECOLOGIC ONCOLOGY, 2005, 97 (01) :96-103
[7]   Expression of cyclooxygenase 2 is an independent prognostic factor in human ovarian carcinoma [J].
Denkert, C ;
Köbel, M ;
Pest, S ;
Koch, I ;
Berger, S ;
Schwabe, M ;
Siegert, A ;
Reies, A ;
Klosterhalfen, B ;
Hauptmann, S .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (03) :893-903
[8]   Pathogenic Role of Cyclooxygenase-2 in Cancer [J].
Divvela, Anantha Krishna Chaitanya ;
Challa, Siva Reddy ;
Tagaram, Israiel Kumar .
JOURNAL OF HEALTH SCIENCE, 2010, 56 (05) :502-516
[9]  
Dixon DA, 2003, PROG EXP TUMOR RES, V37, P52
[10]  
Dugandzija T, 2006, P INT C DIAGN MAN BR