Involvement of Kruppel-like factor 6 (KLF6) mutation in the development of nonpolypoid colorectal carcinoma

被引:21
作者
Mukai, Shinichi
Hiyama, Toru
Tanaka, Shinji
Yoshihara, Masaharu
Arihiro, Koji
Chayama, Kazuaki
机构
[1] Hiroshima Univ Hosp, Dept Endoscopy, Minami Ku, Hiroshima 7348551, Japan
[2] Hiroshima Univ, Grad Sch Biomed Sci, Program Biomed Rres, Div Frontier Med Sci,Dept Med & Mol Sci, Hiroshima, Japan
[3] Hiroshima Univ, Hlth Serv Ctr, Higashihiroshima 724, Japan
[4] Hiroshima Univ, Dept Endoscopy, Hiroshima, Japan
[5] Hiroshima Univ Hosp, Dept Anat Pathol, Hiroshima, Japan
关键词
nonpolypoid colorectal carcinoma; KLF6; p53; K-ras; B-raf;
D O I
10.3748/wjg.v13.i29.3932
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To examine Kruppel-like factor 6 (KLF6) mutations in nonpolypoid-type tumors and alterations of K-ras, p53 and B-raf in relation between mutation and morphologic type, particularly nonpolypoid-type colorectal carcinomas. METHODS: Fifty-five early nonpolypoid colorectal carcinomas were analyzed. Loss of heterozygosity (LOH) of KLF6 and p53 was determined by microsatellite assay. Mutations of KLF6, K-ras, and B-raf were examined by polymerase chain reaction-single-strand conformation polymorphism followed by direct sequencing. In LOH-positive and/or mutation-positive tumors, multiple (4-7) samples in each tumor were microdissected and examined for genetic alterations. p53 expression was evaluated by immunohistochemistry. RESULTS: LOH of KLF6 and p53 was found in 14 of 29 (48.3%) and 14 of 31 (45.2%) tumors, respectively. In 10 of the 14 (71.4%) KLF6 LOH-positive tumors and 9 of the 14 (64.3%) p53 LOH-positive tumors, LOH was found in all of the microdissected samples. In 1 of the 10 (10.0%) KLF6 LOH-positive tumors, a single missense mutation was identified. K-ras and B-raf mutations were found in 5 of 55 (9.1%) and 6 of 55 (10.9%) tumors, respectively. However, these mutations were detected only in subsets of microdissected tumor samples. CONCLUSION: These data suggest that KLF6 and p53 mutations are involved in the development of nonpolypoid colorectal carcinoma, whereas K-ras and B-raf mutations are not. (C) 2007 WJG. All right reserved.
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页码:3932 / 3938
页数:7
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