Immunohistochemical study of the expression of adhesion molecules in ovarian serous neoplasms

被引:78
作者
Cho, EY
Choi, Y
Chae, SW
Sohn, JH
Ahn, GH
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pathol, Seoul 135710, South Korea
[2] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Pathol, Seoul 135710, South Korea
关键词
cell adhesion molecule; ovary; prognosis; serous neoplasms;
D O I
10.1111/j.1440-1827.2006.01925.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
To clarify possible roles of adhesion molecules including E-cadherin, beta- and gamma-catenin, CD44s, CD44v6, CD56, and CD99 in ovarian serous neoplasms, an immunohistochemical study was undertaken for 23 benign, 40 borderline, and 95 malignant ovarian serous neoplasms using tissue microarray (TMA). Significantly reduced expression of E-cadherin, and overexpression of CD44s, CD56, and CD99 were more frequently observed in adenocarcinomas than in benign and borderline tumors. Expression of CD44v6 and nuclear beta- and gamma-catenin were detected only in borderline tumors and adenocarcinomas. Reduced expression of E-cadherin was also correlated with high tumor grade (P = 0.03), presence of peritoneal seeding (P = 0.03), and low overall survival rate (P = 0.02). Overexpression of CD44s was significantly associated with high tumor grade (P = 0.04), advanced stage (P = 0.03), and low overall survival rate (P = 0.02). CD56 was increasingly expressed in the case of advanced stage (P = 0.005) and peritoneal seeding (P = 0.001). Nuclear staining for gamma-catenin was correlated with tumor progression (P = 0.004) and advanced International Federation of Gynecology and Obstetrics (FIGO) stage (P = 0.02). Only CD44s expression and stage were correlated with overall survival in multivariate study. These results suggest that although E-cadherin, CD44s, CD56, and nuclear gamma-catenin immunoexpression seem to be useful prognostic markers for serous neoplasm of the ovary, CD44s expression and FIGO stage are independent prognostic factors.
引用
收藏
页码:62 / 70
页数:9
相关论文
共 45 条
[1]   Coexpression of neural cell adhesion molecules and bcl-2 in intrahepatic cholangiocarcinoma originated from viral hepatitis: Relationship to atypical reactive bile ductule [J].
Asayama, Y ;
Aishima, S ;
Taguchi, K ;
Sugimachi, K ;
Matsuura, S ;
Masuda, K ;
Tsuneyoshi, M .
PATHOLOGY INTERNATIONAL, 2002, 52 (04) :300-306
[2]   Gains and losses of adhesion molecules (CD44, E-cadherin, and β-catenin) during oral carcinogenesis and tumour progression [J].
Bánkfalvi, A ;
Krassort, M ;
Buchwalow, IB ;
Végh, A ;
Felszeghy, E ;
Piffkó, J .
JOURNAL OF PATHOLOGY, 2002, 198 (03) :343-351
[3]  
Bernard G, 1997, J IMMUNOL, V158, P2543
[4]   Molecular genetic alterations in endometrioid carcinomas of the ovary:: Similar frequency of beta-catenin abnormalities but lower rate of microsatellite instability and PTEN alterations than in uterine endometrioid carcinomas [J].
Catasús, L ;
Bussaglia, E ;
Rodríguez, I ;
Gallardo, A ;
Pons, C ;
Irving, JA ;
Prat, J .
HUMAN PATHOLOGY, 2004, 35 (11) :1360-1368
[5]   Alterations of E-cadherin and β-catenin in gastric cancer -: art. no. 16 [J].
Chen, HP ;
Kristjansdottir, S ;
Jonasson, JG ;
Magnusson, J ;
Egilsson, V ;
Ingvarsson, S .
BMC CANCER, 2001, 1 (1)
[6]  
Choi FY, 1998, J IMMUNOL, V161, P749
[7]   An immunohistochemical study of the expression of adhesion molecules in gallbladder lesions [J].
Choi, YL ;
Xuan, YH ;
Shin, YK ;
Chae, SW ;
Kook, MC ;
Sung, RH ;
Youn, SJ ;
Choi, JW ;
Kim, SH .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2004, 52 (05) :591-601
[8]  
Choi YL, 2000, ARCH PATHOL LAB MED, V124, P563
[9]   Altered E-cadherin and epidermal growth factor receptor expressions are associated with patient survival in lung cancer: a study utilizing high-density tissue microarray and immunohistochemistry [J].
Deeb, G ;
Wang, JM ;
Ramnath, N ;
Slocum, HK ;
Wiseman, S ;
Beck, A ;
Tan, DF .
MODERN PATHOLOGY, 2004, 17 (04) :430-439
[10]   CD99 (MIC2) expression in paediatric B-lineage leukaemia lymphoma reflects maturation-associated patterns of normal B-lymphopoiesis [J].
Dworzak, MN ;
Fritsch, G ;
Fleischer, C ;
Printz, D ;
Fröschl, G ;
Buchinger, P ;
Mann, G ;
Gadner, H .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (03) :690-695