Heparanase expression increases throughout the endometrial hyperplasia-cancer sequence

被引:6
作者
Canaani, Jonathan [1 ]
Ilan, Neta [2 ]
Back, Stella [3 ]
Gutman, Guy [1 ]
Davsky, Israel Vl [2 ]
Grisaru, Dan [1 ]
机构
[1] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Dept Obstet & Gynecol, Sackler Fac Med, IL-64239 Tel Aviv, Israel
[2] Technion Israel Inst Technol, Bruce Rappaport Fac Med, Canc & Vasc & Biol Res Ctr, Haifa, Israel
[3] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Dept Pathol, Sackler Fac Med, IL-64239 Tel Aviv, Israel
关键词
endometrial cancer; endometrial hyperplasia; estrogen receptor heparanase; progesterone receptor;
D O I
10.1016/j.ijgo.2007.10.019
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To assess the expression of heparanase in the different stages leading to endometrial cancer. Methods: The 38 examined specimens included adenocarcinoma, hyperplasia, and normal endometrium specimens. Heparanase, estrogen, and progesterone receptor expressions were analyzed immunohistochemically and the intensity was scored. Results: Secretory normal endometrium and simple hyperplasia specimens expressed the lowest mean values of expression (1.00 and 0.63, respectively); the complex hyperplasia specimens and G2 endometrioid adenocarcinoma showed the highest values of expression (2.33 and 2.71, respectively). A linear trend (P=0.005) of heparanase expression was observed when comparing the normal endometrium and simple hyperplasia group with the complex hyperplasia+G1 carcinoma group and the G2+G3 carcinoma group. Evaluation of atrophic and inactive endometrium compared with papillary serous carcinomas yielded no significant differences. We found no significant correlation between heparanase expression and estrogen receptor or progesterone receptor expression. Conclusion: Heparanase expression was tightly regulated in endometrial tumorigenesis. (c) 2007 International Federation of Gynecology and Obstetrics. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:166 / 171
页数:6
相关论文
共 28 条
[1]   Endometrial cancer [J].
Amant, F ;
Moerman, P ;
Neven, P ;
Timmerman, D ;
Van Limbergen, E ;
Vergote, I .
LANCET, 2005, 366 (9484) :491-505
[2]   Prospective multicenter evaluation of the morphometric D-score for prediction of the outcome of endometrial hyperplasias [J].
Baak, JPA ;
Orbo, A ;
van Diest, PJ ;
Jiwa, M ;
de Bruin, P ;
Broeckaert, M ;
Snijders, W ;
Boodt, PJ ;
Fons, G ;
Burger, C ;
Verheijen, RHM ;
Houben, PWH ;
The, HS ;
Kenemans, P .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (07) :930-935
[3]   2 PATHOGENETIC TYPES OF ENDOMETRIAL CARCINOMA [J].
BOKHMAN, JV .
GYNECOLOGIC ONCOLOGY, 1983, 15 (01) :10-17
[4]   Carcinoma of the corpus uteri [J].
Creasman, W. T. ;
Odicino, F. ;
Maisonneuve, P. ;
Quinn, M. A. ;
Beller, U. ;
Benedet, J. L. ;
Heintz, A. P. M. ;
Ngan, H. Y. S. ;
Pecorelli, S. .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2006, 95 :S105-S143
[5]   Spatial and temporal heparanase expression in colon mucosa throughout the adenoma-carcinoma sequence [J].
Doviner, Victoria ;
Maly, Bella ;
Kaplan, Victoria ;
Gingis-Velitski, Svetlana ;
Ilan, Neta ;
Vlodavsky, Israel ;
Sherman, Yoav .
MODERN PATHOLOGY, 2006, 19 (06) :878-888
[6]  
Elkin M, 2003, CANCER RES, V63, P8821
[7]   Expression of heparanase in normal, dysplastic, and neoplastic human colonic mucosa and stroma -: Evidence for its role in colonic tumorigenesis [J].
Friedmann, Y ;
Vlodavsky, I ;
Aingorn, H ;
Aviv, A ;
Peretz, T ;
Pecker, I ;
Pappo, O .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (04) :1167-1175
[8]  
Gohji K, 2001, INT J CANCER, V95, P295, DOI 10.1002/1097-0215(20010920)95:5<295::AID-IJC1051>3.0.CO
[9]  
2-A
[10]  
Hasengaowa, 2006, INT J GYNECOL CANCER, V16, P1401