Value of tenascin-C content and association with clinicopathological parameters in uterine cervical lesions

被引:13
作者
Buyukbayram, H [1 ]
Arslan, A [1 ]
机构
[1] Dicle Univ, Tip Fak, Patol AD, TR-21280 Diyarbakir, Turkey
关键词
tenascin-C; uterine cervix; clinicopathologic parameters; grade; prognosis;
D O I
10.1002/ijc.10546
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To determine whether the content of the matrix protein tenascin-C (Tn-C) is of diagnostic or prognostic value in cervical lesions, we evaluated increases in Tn-C immunoreactivity in 80 formalin-fixed, paraffin-em bedded biopsies and surgical specimens of the uterine cervix. Tn-C content in the basement membrane zone and in the stroma was graded and compared to some prognostic parameters. In the normal cervix, Tn-C formed a thin continuous band. In cervicitis, Tn-C bands thickened in the basement membrane zone and the adjacent stroma in the form of thin filaments. In 30 squamous intraepithelial lesions (SILs) of various grades, Tn-C bands were either slightly (I +) or moderately (2 +) thickened in the basement membrane zone, while slight stromal Tn-C immunoreactivity in the form of thin bands was observed in 12 cases, regardless of grade and inflammatory stromal reaction. In invasive carcinoma, Tn-C content was markedly increased in the stroma and around the invasive nests of tumors. The intensity of Tn-C immunoreactivity was significantly higher in grade I tumors than in others (p < 0.04). The intensity of increase in Tn-C immunoreactivity was 10.5-fold (95% CI 3.39-32.5) higher in invasive cervical carcinomas than in others (cervicitis, low-grade SIL and high-grade SIL) (p = 0.0001). A significant correlation was found between weak Tn-C immunoreactivity and lymphatic space invasion (p = 0.001), lymph node metastasis (p = 0.01), desmoplastic stromal component (p = 0.0001) and stromal inflammation (p = 0.002). In conclusion, increase in Tn-C immunoreactivity may be of value in the assessment of non-invasive and invasive cervical lesions and the appearance of Tn-C may be an indicator of adequate biologic defense in cervical cancer patients. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:719 / 722
页数:4
相关论文
共 27 条
[1]   EPITHELIAL MESENCHYMAL INTERACTIONS IN THE DEVELOPING KIDNEY LEAD TO EXPRESSION OF TENASCIN IN THE MESENCHYME [J].
AUFDERHEIDE, E ;
CHIQUETEHRISMANN, R ;
EKBLOM, P .
JOURNAL OF CELL BIOLOGY, 1987, 105 (01) :599-608
[2]   TENASCIN VARIANTS - DIFFERENTIAL BINDING TO FIBRONECTIN AND DISTINCT DISTRIBUTION IN CELL-CULTURES AND TISSUES [J].
CHIQUETEHRISMANN, R ;
MATSUOKA, Y ;
HOFER, U ;
SPRING, J ;
BERNASCONI, C ;
CHIQUET, M .
CELL REGULATION, 1991, 2 (11) :927-938
[3]  
EKBLOM P, 1989, International Journal of Developmental Biology, V33, P71
[4]   IMMUNOHISTOCHEMICAL EXPRESSION OF TENASCIN IN NORMAL STOMACH TISSUE, GASTRIC CARCINOMAS AND GASTRIC-CARCINOMA IN LYMPH-NODES [J].
IKEDA, Y ;
MORI, M ;
KAJIYAMA, K ;
HARAGUCHI, Y ;
SASAKI, O ;
SUGIMACHI, K .
BRITISH JOURNAL OF CANCER, 1995, 72 (01) :189-192
[5]  
Ishihara A, 1995, CLIN CANCER RES, V1, P1035
[6]  
Iskaros BF, 1997, J SURG ONCOL, V64, P98, DOI 10.1002/(SICI)1096-9098(199702)64:2<98::AID-JSO2>3.0.CO
[7]  
2-J
[8]  
Iskaros BF, 2000, ARCH PATHOL LAB MED, V124, P1282
[9]  
Iskaros BF, 1998, J SURG ONCOL, V68, P107
[10]  
Jahkola T, 1996, INT J CANCER, V69, P445, DOI 10.1002/(SICI)1097-0215(19961220)69:6<445::AID-IJC4>3.3.CO