Collagen type XVIII/endostatin is differentially expressed in primary and metastatic colorectal cancers and ovarian carcinomas

被引:17
作者
Guenther, U
Herbst, H
Bauer, M
Isbert, C
Buhr, HJ
Riecken, EO
Schuppan, D
机构
[1] Free Univ Berlin, Benjamin Franklin Hosp, Dept Gastroenterol, D-1000 Berlin, Germany
[2] Free Univ Berlin, Benjamin Franklin Hosp, Dept Surg, D-1000 Berlin, Germany
[3] Univ Munster, Gerhard Domagk Inst Pathol, D-4400 Munster, Germany
[4] Univ Erlangen Nurnberg, Dept Gastroenterol & Hepatol, Erlangen, Germany
关键词
angiogenesis inhibition; cancer; liver; ovary; tumour therapy;
D O I
10.1054/bjoc.2001.2143
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Collagen type XVIII (C18) is a nonfibrillar collagen of basement membranes. Its C-terminal fragment, endostatin, has been identified as an inhibitor of angiogenesis. C18 is predominantly expressed by hepatocytes of normal, cirrhotic and neoplastic liver. We compared the patterns of C18 RNA-expression in colonic adenocarcinoma metastases, which represent the most frequently occurring liver tumours, to normal colon mucosa, to primary colon cancers and to ovarian cancers which are often morphologically similar to colonic cancer or metastasis. Two C18-specific RNA-probes were generated to perform in situ hybridization combined with immunohistochemistry for cytokeratin, vimentin and the endothelial marker CD31, in order to characterize the C18-expressing cells. C18/endostatin protein was localized by immunohistology. In colorectal carcinomas and their liver metastases high levels of C18 transcripts were observed in endothelial cells and fibroblasts/myofibroblasts, whereas C18 RNA was virtually absent from carcinoma cells. Ovarian carcinomas displayed high C18 RNA expression both in carcinoma and stromal cells, indicating that induction of C18 transcription in tumour stromal cells is independent of the ability of carcinoma cells to express C18. While the role of tumour cell derived C18 in cancer growth regulation remains unknown, stimulation of proteolysis of the locally strongly expressed C18 to endostatin could offer an attractive approach for a targeted antineoplastic therapy. (C) 2001 Cancer Research Campaign.
引用
收藏
页码:1540 / 1545
页数:6
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