Up-regulation of macrophage wnt gene expression in adenoma-carcinoma progression of human colorectal cancer

被引:96
|
作者
Smith, K [1 ]
Bui, TD
Poulsom, R
Kaklamanis, L
Williams, G
Harris, AL
机构
[1] John Radcliffe Hosp, Imperial Canc Res Fund, Oncol Mol Lab, Oxford, England
[2] Nuffield Orthopaed Hosp, Wellcome Trust, Oxford, England
[3] Onassis Cardiac Surg Ctr, Dept Pathol, Athens 17674, Greece
[4] Imperial Canc Res Fund, Histopathol Unit, London WC2A 3PX, England
基金
英国惠康基金;
关键词
human colorectal cancer; in situ hybridization; macrophages; tumour progression; wnt genes;
D O I
10.1038/sj.bjc.6690721
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Defects in the APC-beta-catenin pathway are common in colon cancer. We investigated whether aberrant regulation of upstream ligands stimulating this pathway occur in colon cancer. Using RNAase protection analysis, six out of eight wnt genes were expressed in 14 matched cases of normal, adenomatous and malignant colorectal tissues. Wnt 2 and wnt 5a were significantly up-regulated in the progression from normal through adenoma to carcinoma. Transcripts for wnts 4, 7b, 10b and 13, but not wnt 2 and wnt 5a were detected in several colorectal cell lines. in situ hybridization demonstrated that wnt 2 and wnt 5a transcripts were mainly in the lamina propria/stroma region with labelling predominantly in macrophages. Immunostaining with CD68 confirmed the wnt-expressing cells as macrophages. These results show a major difference in wnt expression in colon cancer compared to colon adenomas and suggest stromal wnt expression may play a role in tumour progression. (C) 1999 Cancer Research Campaign.
引用
收藏
页码:496 / 502
页数:7
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