Differential roles of EPS8 in carcinogenesis: Loss of protein expression in a subset of colorectal carcinoma and adenoma

被引:16
作者
Abdel-Rahman, Wael M. [1 ,2 ]
Ruosaari, Saila [3 ,4 ]
Knuutila, Sakari [3 ,4 ]
Peltomaki, Paivi [2 ]
机构
[1] Univ Sharjah, Coll Hlth Sci, Dept Med Lab Sci, Sharjah 27272, U Arab Emirates
[2] Univ Helsinki, Dept Med Genet, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Dept Pathol, Haartman Inst, FIN-00014 Helsinki, Finland
[4] Univ Helsinki, Cent Hosp, HUSLAB, FIN-00014 Helsinki, Finland
基金
欧洲研究理事会; 芬兰科学院;
关键词
Actin capping; Colon cancer; Epidermal growth factor receptor pathway substrate 8; Hypermethylation; Immunohistochemistry; RKO; ACTIN-FILAMENTS; MISMATCH REPAIR; CELL-LINES; CANCER; ENDOMETRIAL; SIGNALS; RAC; ACTIVATION; MUTATIONS; MOTILITY;
D O I
10.3748/wjg.v18.i29.3896
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To analyze the epidermal growth factor receptor pathway substrate 8 (EPS8) expression status and role in colorectal carcinogenesis given that EPS8 has a conserved actin barbed-end capping function that is required for proper maturation in intestinal cells. METHODS: We studied 8 colon cancer cell lines and 58 colorectal tumors (19 adenomas and 39 carcinomas). We performed expression microarray analysis of colon cancer cell lines followed by loss of heterozygosity (LOH) analysis and immunohistochemistry for EPS8 expression in colon tumors. Subsequently, we performed mutation analysis by direct sequencing and methylation analysis by bisulfite sequencing and methylation-specific polymerase chain reaction assays. RESULTS: Expression microarray analysis of colon cancer cell lines showed overexpression of EPS8 transcript in all lines but RKO. Genome wide loss of heterozygosity (LOH) analysis of colon tumors, showed considerable LOH at the EPS8 gene locus. Immunohistochemically, EPS8 was constitutively expressed in normal colonic mucosa with a dot-like supranuclear localization with accentuation at the luminal surface supporting its proposed role in epithelial maturation. Nineteen colon tumors (4 adenoma, 15 carcinoma) out of 51 (37%) showed strikingly tumor specific EPS8 protein loss. Of the remaining tumors, 5/51 (2 adenoma, and 3 carcinoma, 10%) showed marked overexpression, while 27/51 tumors (53%) showed retained expression. Mutation analysis revealed a missense mutation (c.794C>T, p.R265C) in exon 8 in RKO. The EP58 promoter was also methylated in RKO, but there was no significant methylation in other cell lines or carcinoma specimens. CONCLUSION: The loss of EPS8 expression in colorectal adenomas and carcinomas suggests that down regulation of this gene contributes to the development of a subset of colorectal cancers, a finding which could have applications in diagnosis and treatment. (C) 2012 Baishideng. All rights reserved.
引用
收藏
页码:3896 / 3903
页数:8
相关论文
共 27 条
[1]
Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous β-catenin [J].
Abdel-Rahman, Wael M. ;
Kalinina, Juliya ;
Shoman, Soheir ;
Eissa, Saad ;
Ollikainen, Miina ;
Elomaa, Outi ;
Eliseenkova, Anna V. ;
Butzow, Ralf ;
Mohammadi, Moosa ;
Peltomaki, Paivi .
HUMAN MUTATION, 2008, 29 (03) :390-397
[2]
Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations [J].
Abdel-Rahman, WM ;
Ollikainen, M ;
Kariola, R ;
Järvinen, HJ ;
Mecklin, JP ;
Nyström-Lahti, M ;
Knuutila, S ;
Peltomäki, P .
ONCOGENE, 2005, 24 (09) :1542-1551
[3]
Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number [J].
Abdel-Rahman, WM ;
Lohi, H ;
Knuttila, S ;
Peltomäki, P .
ONCOGENE, 2005, 24 (04) :706-713
[4]
Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement [J].
Abdel-Rahman, WM ;
Katsura, K ;
Rens, W ;
Gorman, PA ;
Sheer, D ;
Bicknell, D ;
Bodmer, WF ;
Arends, MJ ;
Wyllie, AH ;
Edwards, PAW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2538-2543
[5]
Betts MJ, 2003, Bioinformatics for geneticists, P289, DOI [10.1002/0470867302.CH14, DOI 10.1002/0470867302.CH14]
[6]
Eps8 decreases chemosensitivity and affects survival of cervical cancer patients [J].
Chen, Yun-Ju ;
Shen, Meng-Ru ;
Chen, Yen-Jen ;
Maa, Ming-Chei ;
Leu, Tzeng-Horng .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (06) :1376-1385
[7]
A novel actin barbed-end-capping activity in EPS-8 regulates apical morphogenesis in intestinal cells of Caenorhabditis elegans [J].
Croce, A ;
Cassata, G ;
Disanza, A ;
Gagliani, MC ;
Tacchetti, C ;
Malabarba, MG ;
Carlier, MF ;
Scita, G ;
Baumeister, R ;
Di Fiore, PP .
NATURE CELL BIOLOGY, 2004, 6 (12) :1173-1179
[8]
CDX2 is mutated in a colorectal cancer with normal APC/β-catenin signaling [J].
da Costa, LT ;
He, TC ;
Yu, J ;
Sparks, AB ;
Morin, PJ ;
Polyak, K ;
Laken, S ;
Vogelstein, B ;
Kinzler, KW .
ONCOGENE, 1999, 18 (35) :5010-5014
[9]
Eps8 controls actin-based motility by capping the barbed ends of actin filaments [J].
Disanza, A ;
Carlier, MF ;
Stradal, TEB ;
Didry, D ;
Frittoli, E ;
Confalonieri, S ;
Croce, A ;
Wehland, J ;
Di Fiore, PP ;
Scita, G .
NATURE CELL BIOLOGY, 2004, 6 (12) :1180-1188
[10]
EPS8, A SUBSTRATE FOR THE EPIDERMAL GROWTH-FACTOR RECEPTOR KINASE, ENHANCES EGF-DEPENDENT MITOGENIC SIGNALS [J].
FAZIOLI, F ;
MINICHIELLO, L ;
MATOSKA, V ;
CASTAGNINO, P ;
MIKI, T ;
WONG, WT ;
DIFIORE, PP .
EMBO JOURNAL, 1993, 12 (10) :3799-3808