Wnt pathway-related gene expression in inflammatory bowel disease

被引:107
作者
You, Joann [2 ]
Nguyen, Anthony V. [2 ]
Albers, C. Gregory [3 ]
Lin, Fritz [3 ]
Holcombe, Randall F. [1 ,2 ]
机构
[1] Univ Calif Irvine, Div Hematol Oncol, Irvine Med Ctr, Orange, CA 92868 USA
[2] Univ Calif Irvine, Div Hematol Oncol, Chao Family Comprehens Canc Ctr, Orange, CA 92868 USA
[3] Univ Calif Irvine, Div Gastroenterol, Dept Pathol, Orange, CA 92868 USA
关键词
Wnt signaling; colon cancer; inflammatory bowel disease; ulcerative colitis; microarray analysis;
D O I
10.1007/s10620-007-9973-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The purpose of this study was to examine the expression of Wnt pathway-related genes in patients with ulcerative colitis (UC). RNA from colonoscopic biopsies from noninflammatory bowel disease (non-IBD) subjects and UC patients were obtained and examined with a Wnt-specific microarray for the expression of Wnt pathway-related genes. Paired samples from uninflamed and inflamed areas of the colon were obtained for the UC patients. WNT2B, WNT3A, WNT5B, WNT6, WNT7A, WNT9A, and WNT11 exhibited significantly increased expression in UC compared to non-IBD patients. Frizzled 3 (FZD3) and FZD4 exhibited significantly increased expression, and FZD1 and FZD5 exhibited significantly decreased expression in UC patients. Genes with increased expression in inflamed mucosa included DKK4, DVL2, SOX17, and COL1A1. There was no difference in the expression of a panel of Wnt target genes. The expression of inducible nitric oxide synthase (INOS) was variably influenced by inflammation. Significant differences in extracellular and cell-surface components of the Wnt pathway exist in the colonic mucosa of patients with UC compared with non-IBD patients, which may influence the strength or specificity of Wnt signaling. In inflammation, inhibitory components of the Wnt pathway exhibit increased expression, but no changes in Wnt pathway target gene expression are seen. The role and complex regulation of Sox17 and iNOS in IBD warrant further investigation.
引用
收藏
页码:1013 / 1019
页数:7
相关论文
共 40 条
[1]
The APC/β-catenin pathway in ulcerative colitis-related colorectal carcinomas -: A mutational analysis [J].
Aust, DE ;
Terdiman, JP ;
Willenbucher, RF ;
Chang, CG ;
Molinaro-Clark, A ;
Baretton, GB ;
Loehrs, U ;
Waldman, FM .
CANCER, 2002, 94 (05) :1421-1427
[2]
Interaction of frizzled related protein (FRP) with Wnt ligands and the frizzled receptor suggests alternative mechanisms for FRP inhibition of Wnt signaling [J].
Bafico, A ;
Gazit, A ;
Pramila, T ;
Finch, PW ;
Yaniv, A ;
Aaronson, SA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (23) :16180-16187
[3]
Functional interaction of beta-catenin with the transcription factor LEF-1 [J].
Behrens, J ;
vonKries, JP ;
Kuhl, M ;
Bruhn, L ;
Wedlich, D ;
Grosschedl, R ;
Birchmeier, W .
NATURE, 1996, 382 (6592) :638-642
[4]
Wnt signaling: a common theme in animal development [J].
Cadigan, KM ;
Nusse, R .
GENES & DEVELOPMENT, 1997, 11 (24) :3286-3305
[5]
WNT signaling in the normal intestine and colorectal cancer [J].
de Lau, Wim ;
Barker, Nick ;
Clevers, Hans .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2007, 12 :471-491
[6]
Regulation of human nitric oxide synthase 2 expression by Wnt β-catenin signaling [J].
Du, Qiang ;
Park, Kyung Soo ;
Guo, Zhong ;
He, Peijun ;
Nagashima, Makoto ;
Shao, Lifang ;
Sahai, Rohit ;
Geller, David A. ;
Hussain, S. Perwez .
CANCER RESEARCH, 2006, 66 (14) :7024-7031
[7]
Identification of c-MYC as a target of the APC pathway [J].
He, TC ;
Sparks, AB ;
Rago, C ;
Hermeking, H ;
Zawel, L ;
da Costa, LT ;
Morin, PJ ;
Vogelstein, B ;
Kinzler, KW .
SCIENCE, 1998, 281 (5382) :1509-1512
[8]
Expression of Wnt ligands and Frizzled receptors in colonic mucosa and in colon carcinoma [J].
Holcombe, RF ;
Marsh, JL ;
Waterman, ML ;
Lin, F ;
Milovanovic, T ;
Truong, T .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2002, 55 (04) :220-226
[9]
β-catenin–sensitive isoforms of lymphoid enhancer factor-1 are selectively expressed in colon cancer [J].
Karine Hovanes ;
Tony W.H. Li ;
Jesus E. Munguia ;
Trung Truong ;
Tatjana Milovanovic ;
J. Lawrence Marsh ;
Randall F. Holcombe ;
Marian L. Waterman .
Nature Genetics, 2001, 28 (1) :53-57
[10]
Howe LR, 1999, CANCER RES, V59, P1572