Expression of claudins 1, 4, 5, and 7 in ovarian tumors of diverse types

被引:35
作者
Soini, Ylermi
Talvensaari-Mattila, Anne
机构
[1] Oulu Univ Hosp, Dept Pathol, Oulu, Finland
[2] Oulu Univ Hosp, Dept Obstet & Gynecol, Oulu, Finland
关键词
adhesion; tight junction; ovary; carcinoma;
D O I
10.1097/01.pgp.0000215298.38114.cc
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
In this study, 60 different types of ovarian lesions, mainly consisting of ovarian neoplasms, were studied for the expression of claudins 1, 4, 5, and 7. Strong expression of claudins 1, 4, and 7 was seen in benign and malignant epithelial ovarian tumors. Expression of claudin 5, reported to be mainly present in endothelial cells, was seen in ovarian epithelial tumors, but with a significantly lower frequency than claudins 1, 4, and 7. On the contrary, sex-cord stromal tumors and cysts, such as fibromas/thecomas, Sertoli-Leydig cell tumors, granulosa cell tumors, and follicular and luteinized cysts were mainly negative for claudins 1, 4, 5, and 7. Interestingly, adenomatoid tumors did not express claudin 5, which is in agreement with their non-endothelial nature. They were also negative for claudin 4, but expressed claudins 1 and 7, but to a lesser degree than epithelial lesions. In immature teratomas, the epithelial component was usually positive whereas other components were negative for these claudins. Dysgerminomas did not express any of the claudins studied. The results show that claudins 1, 4, and 7 are mainly expressed in ovarian epithelial tumors and can thus be used to indicate epithelial differentiation in them. Eventhough considered an endothelial marker, claudin 5 was also present in a subset of epithelial lesions. However, this claudin can be used to differentiate adenomatoid tumors from vascular lesions. No significant difference was seen between epithelial benign and malignant lesions, except for claudin 5, which seemed stronger in malignant epithelial tumors.
引用
收藏
页码:330 / 335
页数:6
相关论文
共 21 条
[1]  
Bronstein JM, 2000, J NEUROSCI RES, V60, P284, DOI 10.1002/(SICI)1097-4547(20000501)60:3<284::AID-JNR2>3.3.CO
[2]  
2-K
[3]   Expression of claudin-1, a recently described tight junction-associated protein, distinguishes soft tissue perineurioma from potential mimics [J].
Folpe, AL ;
Billings, SD ;
McKenney, JK ;
Walsh, SV ;
Nusrat, A ;
Weiss, SW .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2002, 26 (12) :1620-1626
[4]   Clostridium perfringens enterotoxin elicits rapid and specific cytolysis of breast carcinoma cells mediated through tight junction proteins claudin 3 and 4 [J].
Kominsky, SL ;
Vali, M ;
Korz, D ;
Gabig, TG ;
Weitzman, SA ;
Argani, P ;
Sukumar, S .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (05) :1627-1633
[5]  
Long HY, 2001, CANCER RES, V61, P7878
[6]   Selection of potential markers for epithelial ovarian cancer with gene expression arrays and recursive descent partition analysis [J].
Lu, KH ;
Patterson, AP ;
Wang, L ;
Marquez, RT ;
Atkinson, EN ;
Baggerly, KA ;
Ramoth, LR ;
Rosen, DG ;
Liu, JS ;
Hellstrom, I ;
Smith, D ;
Hartmann, L ;
Fishman, D ;
Berchuck, A ;
Schmandt, R ;
Whitaker, R ;
Gershenson, DM ;
Mills, GB ;
Bast, RC .
CLINICAL CANCER RESEARCH, 2004, 10 (10) :3291-3300
[7]   Claudin-4:: A new target for pancreatic cancer treatment using Clostridium perfringens enterotoxin [J].
Michl, P ;
Buchholz, M ;
Rolke, M ;
Kunsch, S ;
Löhr, M ;
McClane, B ;
Tsukita, S ;
Leder, G ;
Adler, G ;
Gress, TM .
GASTROENTEROLOGY, 2001, 121 (03) :678-684
[8]   Molecular Physiology and Pathophysiology of Tight Junctions - I. Tight junction structure and function: lessons from mutant animals and proteins [J].
Mitic, LL ;
van Itallie, CM ;
Anderson, JM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 279 (02) :G250-G254
[9]  
Rangel LBA, 2003, CLIN CANCER RES, V9, P2567
[10]   The renal segmental distribution of claudins changes with development [J].
Reyes, JL ;
Lamas, M ;
Martin, D ;
Namorado, MD ;
Islas, S ;
Luna, J ;
Tauc, M ;
González-Mariscal, L .
KIDNEY INTERNATIONAL, 2002, 62 (02) :476-487