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.
引用
收藏
页码:3932 / 3938
页数:7
相关论文
共 24 条
[11]   BRAF mutations and phosphorylation status of mitogen-activated protein kinases in the development of flat and depressed-type colorectal neoplasias [J].
Konishi, K ;
Takimoto, M ;
Kaneko, K ;
Makino, R ;
Hirayama, Y ;
Nozawa, H ;
Kurahashi, T ;
Kumekawa, Y ;
Yamamoto, T ;
Ito, H ;
Yoshikawa, N ;
Kusano, M ;
Nakayama, K ;
Rembacken, BJ ;
Ota, H ;
Imawari, M .
BRITISH JOURNAL OF CANCER, 2006, 94 (02) :311-317
[12]   THE PROBLEM OF DE-NOVO COLORECTAL-CARCINOMA [J].
KUDO, S ;
TAMURA, S ;
HIROTA, S ;
SANO, Y ;
YAMANO, H ;
SERIZAWA, M ;
FUKUOKA, T ;
MITSUOKA, H ;
NAKAJIMA, T ;
KUSAKA, H .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (7-8) :1118-1120
[13]  
MUTO T, 1985, DIS COLON RECTUM, V28, P847, DOI 10.1007/BF02555490
[14]   KLF6, a candidate tumor suppressor gene mutated in prostate cancer [J].
Narla, G ;
Heath, KE ;
Reeves, HL ;
Li, D ;
Giono, LE ;
Kimmelman, AC ;
Glucksman, MJ ;
Narla, J ;
Eng, FJ ;
Chan, AM ;
Ferrari, AC ;
Martignetti, JA ;
Friedman, SL .
SCIENCE, 2001, 294 (5551) :2563-2566
[15]  
Noda H, 2006, J EXP CLIN CANC RES, V25, P235
[16]   Kruppel-Like factor 6 (KLF6) is a tumor-suppressor gene frequently inactivated in colorectal cancer [J].
Reeves, HL ;
Narla, G ;
Ogunbiyi, O ;
Haq, AI ;
Katz, A ;
Benzeno, S ;
Hod, E ;
Harpaz, N ;
Goldberg, S ;
Tal-Kremer, S ;
Eng, FJ ;
Arthur, MJP ;
Martignetti, JA ;
Friedman, SL .
GASTROENTEROLOGY, 2004, 126 (04) :1090-1103
[17]   Frequent hypermethylation of RASSF1A in early flat-type colorectal tumors [J].
Sakamoto, N ;
Terai, T ;
Ajioka, Y ;
Abe, S ;
Kobayasi, O ;
Hirai, S ;
Hino, O ;
Watanabe, H ;
Sato, N ;
Shimoda, T ;
Fujii, H .
ONCOGENE, 2004, 23 (55) :8900-8907
[18]  
Shima H, 2006, ONCOL REP, V16, P685
[19]  
SHIMODA T, 1989, CANCER, V64, P1138, DOI 10.1002/1097-0142(19890901)64:5<1138::AID-CNCR2820640529>3.0.CO
[20]  
2-A