Kim H, Yang X L, Rosada C, Hamilton S R, August J T
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Arch Biochem Biophys. 1994 May 1;310(2):504-7. doi: 10.1006/abbi.1994.1199.
Neoplastic progression of colorectal epithelial cells from benign adenomas to malignant carcinomas appears to result from a series of genetic alterations involving both oncogenes and tumor suppressor genes. This progression was recently found to be associated with expression of splice variant isoforms of CD44, a cell surface hyaluronate receptor implicated in carcinogenesis. In this study we examined the relationship of CD44 expression to somatic genetic events in the adenoma-carcinoma sequence: point mutation of K-ras in codons 12 and 13 and overexpression of p53 protein as a marker of gene mutation. Among 22 small adenomas, CD44 was present in 9 (41%), of which only 1 contained a K-ras mutation. CD44 was absent in the other 2 small adenomas positive for K-ras mutation or p53 overexpression. In contrast to the early expression of CD44 in small adenomas, mutations of K-ras and p53 were detected preferentially in large adenomas and late-stage adenomas containing carcinoma. The frequent expression of CD44 prior to K-ras and p53 gene alterations in colorectal neoplasia suggests that activation of CD44 gene expression is related to earlier events in the adenoma-carcinoma sequence, possibly cell activation and proliferation following APC gene mutation or alteration of DNA methylation.
结直肠上皮细胞从良性腺瘤向恶性癌的肿瘤进展似乎是由一系列涉及癌基因和肿瘤抑制基因的基因改变所致。最近发现这种进展与CD44剪接变异体亚型的表达相关,CD44是一种参与致癌作用的细胞表面透明质酸受体。在本研究中,我们检测了腺瘤-癌序列中CD44表达与体细胞遗传事件的关系:K-ras基因第12和13密码子的点突变以及p53蛋白过表达作为基因突变的标志物。在22个小腺瘤中,9个(41%)存在CD44,其中只有1个含有K-ras突变。在其他2个K-ras突变或p53过表达阳性的小腺瘤中未检测到CD44。与CD44在小腺瘤中的早期表达相反,K-ras和p53突变在大腺瘤和含有癌的晚期腺瘤中优先被检测到。在结直肠肿瘤中CD44基因表达在K-ras和p53基因改变之前频繁出现,这表明CD44基因表达的激活与腺瘤-癌序列中的早期事件相关,可能是APC基因突变或DNA甲基化改变后的细胞激活和增殖。