Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours

被引:37
作者
Wilson, KE [1 ]
Langdon, SP [1 ]
Lessells, AM [1 ]
Miller, WR [1 ]
机构
[1] WESTERN GEN HOSP, DEPT PATHOL, EDINBURGH EH4 2XU, MIDLOTHIAN, SCOTLAND
关键词
tenascin; extracellular matrix; ovarian cancer;
D O I
10.1038/bjc.1996.480
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The extracellular matrix protein tenascin (TN) is overexpressed in a number of solid tumours. This, however, is the first study to examine TN expression in ovarian tumours. TN protein was examined in frozen sections of 50 human ovarian tumours by immunohistochemistry. Malignant and borderline tumours showed a significantly greater incidence and intensity of stromal staining than benign tumours (P < 0.0001 and P = 0.038 respectively). Seven omental metastases were also examined and showed a strikingly similar protein distribution to their primary tumour counterparts. The expression pattern of different RNA isoforms, created by alternative splicing of the primary transcript, was identified using reverse transcription-polymerase chain reactions (RT-PCR). The smallest TN RNA splice variant (284 bp) was found in all tumours examined, while the appearance of larger molecular weight transcripts (similar to 490 and 556 bp), as major forms, was predominantly limited to malignant tumours, with 9/12 malignant tumours showing this pattern compared with 1/6 benign tumours. These data suggest that malignant ovarian tumours have increased expression of TN compared with benign tumours and this may be associated with induction of specific isoforms.
引用
收藏
页码:999 / 1004
页数:6
相关论文
共 29 条
[1]   CELL-CYCLE DEPENDENT ALTERNATIVE SPLICING OF THE TENASCIN PRIMARY TRANSCRIPT [J].
BORSI, L ;
BALZA, E ;
CASTELLANI, P ;
CARNEMOLLA, B ;
PONASSI, M ;
QUERZE, G ;
ZARDI, L .
CELL ADHESION AND COMMUNICATION, 1994, 1 (04) :307-317
[2]   THE ALTERNATIVE SPLICING PATTERN OF THE TENASCIN-C PRE-MESSENGER-RNA IS CONTROLLED BY THE EXTRACELLULAR PH [J].
BORSI, L ;
BALZA, E ;
GAGGERO, B ;
ALLEMANNI, G ;
ZARDI, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :6243-6245
[3]   EXPRESSION OF DIFFERENT TENASCIN ISOFORMS IN NORMAL, HYPERPLASTIC AND NEOPLASTIC HUMAN BREAST TISSUES [J].
BORSI, L ;
CARNEMOLLA, B ;
NICOLO, G ;
SPINA, B ;
TANARA, G ;
ZARDI, L .
INTERNATIONAL JOURNAL OF CANCER, 1992, 52 (05) :688-692
[4]   TENASCIN - AN EXTRACELLULAR-MATRIX PROTEIN INVOLVED IN TISSUE INTERACTIONS DURING FETAL DEVELOPMENT AND ONCOGENESIS [J].
CHIQUETEHRISMANN, R ;
MACKIE, EJ ;
PEARSON, CA ;
SAKAKURA, T .
CELL, 1986, 47 (01) :131-139
[5]   TENASCIN INTERFERES WITH FIBRONECTIN ACTION [J].
CHIQUETEHRISMANN, R ;
KALLA, P ;
PEARSON, CA ;
BECK, K ;
CHIQUET, M .
CELL, 1988, 53 (03) :383-390
[6]  
CHIQUETEHRISMANN R, 1989, CANCER RES, V49, P4322
[7]   TENASCIN - AN EXTRACELLULAR-MATRIX PROTEIN PROMINENT IN SPECIALIZED EMBRYONIC-TISSUES AND TUMORS [J].
ERICKSON, HP ;
BOURDON, MA .
ANNUAL REVIEW OF CELL BIOLOGY, 1989, 5 :71-92
[8]   TENASCIN DISTRIBUTION IN THE NORMAL HUMAN BREAST IS ALTERED DURING THE MENSTRUAL-CYCLE AND IN CARCINOMA [J].
FERGUSON, JE ;
SCHOR, AM ;
HOWELL, A ;
FERGUSON, MWJ .
DIFFERENTIATION, 1990, 42 (03) :199-207
[9]   AN ALTERNATIVELY SPLICED REGION OF THE HUMAN HEXABRACHION CONTAINS A REPEAT OF POTENTIAL N-GLYCOSYLATION SITES [J].
GULCHER, JR ;
NIES, DE ;
MARTON, LS ;
STEFANSSON, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (05) :1588-1592
[10]  
HOWEEDY AA, 1990, LAB INVEST, V63, P498