Cyclooxygenase-2 overexpression is related to polypoid growth and K-ras gene mutation in T1 colorectal carcinomas

被引:5
|
作者
Okawa, T
Yoshinaga, K
Uetake, H
Sato, T
Higuchi, T
Nemoto, T
Sugihara, K
机构
[1] Tokyo Med & Dent Univ, Dept Digest Surg, Grad Sch, Bunkyo Ku, Tokyo 1138519, Japan
[2] Natl Printing Bur Tokyo Hosp, Dept Surg, Tokyo, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Dept Human Pathol, Tokyo, Japan
关键词
morphology; polypoid growth carcinoma; nonpolypoid growth carcinoma; co-;
D O I
10.1007/s10350-004-0684-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
PURPOSE: Cyclooxygenase-2 is thought to play a role in the development of intestinal tumors and levels are elevated in approximately 80 to 90 percent of human colorectal carcinomas. To clarify the role that cyclooxygenase-2 plays in the development of colorectal carcinoma, we studied the relationship between cyclooxygenase-2 expression and tumor morphology and that between cyclooxygenase-2 expression and K-ras mutation. METHODS: We classified 48 T1 colorectal carcinomas as polypoid or nonpolypoid and analyzed the clinicopathologic features. The expression of cyclooxygenase-2 was determined immunohistochemically, and nested polymerase chain reaction-restriction fragment length polymorphism detected a K-ras codon 12 mutation. RESULTS: Cyclooxygenase-2 expression was higher in polypoid carcinomas than in nonpolypoid carcinomas (P < 0.001). The K-ras codon 12 mutation was associated with higher levels of cyclooxygenase-2 expression compared with carcinomas without this mutation (P = 0.028). CONCLUSIONS: Polypoid growth and K-ras gene mutation are both associated with increased levels of cyclooxygenase-2 expression in T1 tumors.
引用
收藏
页码:1915 / 1921
页数:7
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