Smith K, Bui T D, Poulsom R, Kaklamanis L, Williams G, Harris A L
ICRF Molecular Oncology Laboratory, John Radcliffe Hospital, Oxford, UK.
Br J Cancer. 1999 Oct;81(3):496-502. doi: 10.1038/sj.bjc.6690721.
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.
APC-β-连环蛋白信号通路缺陷在结肠癌中很常见。我们研究了刺激该信号通路的上游配体在结肠癌中是否存在异常调节。通过核糖核酸酶保护分析,在14例匹配的正常、腺瘤性和恶性结直肠组织中,8个Wnt基因中有6个表达。从正常组织到腺瘤再到癌的进展过程中,Wnt 2和Wnt 5a显著上调。在几种结肠直肠癌细胞系中检测到了Wnts 4、7b、10b和13的转录本,但未检测到Wnt 2和Wnt 5a的转录本。原位杂交显示,Wnt 2和Wnt 5a转录本主要位于固有层/基质区域,主要在巨噬细胞中标记。用CD68进行免疫染色证实表达Wnt的细胞为巨噬细胞。这些结果表明,与结肠腺瘤相比,结肠癌中Wnt表达存在重大差异,并提示基质Wnt表达可能在肿瘤进展中起作用。