In colon carcinogenesis, the cytosketetal protein gelsolin is down-regulated during the transition from adenoma to carcinoma

被引:32
作者
Gay, Fabien [1 ,2 ,3 ,4 ]
Estornes, Yann [1 ,2 ,3 ,4 ]
Saurin, Jean-Christophe [1 ,2 ,3 ,4 ]
Joly-Pharaboz, Marie-Odile [1 ,2 ,3 ,4 ,5 ]
Friederich, Evelyne [6 ]
Scoazec, Jean-Yves [1 ,2 ,3 ,4 ,5 ]
Abello, Jacques [1 ,2 ,3 ,4 ]
机构
[1] INSERM, U865, F-69372 Lyon, France
[2] INSERM, IFR62, F-69372 Lyon, France
[3] Univ Lyon, F-69003 Lyon, France
[4] Univ Lyon 1, F-69372 Villeurbanne, France
[5] Hop Edouard Herriot, Hosp Civils Lyon, Serv Cent Anat & Cytol Pathol, F-69437 Lyon, France
[6] Univ Luxembourg, Dept Life Sci, L-1511 Luxembourg, Luxembourg
关键词
gelsolin; immunohistochemistry; adenoma; adenocarcinoma; colon;
D O I
10.1016/j.humpath.2008.02.020
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
The actin-binding protein gelsolin is involved in cell motility via the regulation of actin cytoskeleton, and its expression is modified in several human cancers. However, the potential implication of this protein in colorectal carcinogenesis is debated. By using immumohistochemistry, we studied gelsolin expression in 69 cases of colon adenocarcinomas and in 72 lesions representative of the different stages of colonic tumorigenesis. In addition, we performed Northern blot analysis of gelsolin messenger RNA in 12 paired samples of human colon cancer and normal corresponding mucosa. Gelsolin protein and messenger RNA expressions were severely down-regulated in all adenocarcinomas tested. Moreover, gelsolin protein was down-regulated in a large proportion of high-grade adenomas (14/16) before the acquisition of invasive properties but in only a small proportion of low grade adenomas and serrated adenomas (2/30) and in none of the 9 cases of nonneoplastic hyperplastic polyps tested. Our results therefore demonstrate that gelsolin down-regulation is an early and almost constant event in colon carcinogenesis and is associated with the transition from adenoma to carcinoma. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1420 / 1430
页数:11
相关论文
共 39 条
[1]
[Anonymous], WHO CLASS TUM PATH G
[2]
Gelsolin is a downstream effector of rac for fibroblast motility [J].
Azuma, T ;
Witke, W ;
Stossel, TT ;
Hartwig, JH ;
Kwiatkowski, DJ .
EMBO JOURNAL, 1998, 17 (05) :1362-1370
[3]
Gene expression profiling of colon cancer by DNA microarrays and correlation with histoclinical parameters [J].
Bertucci, F ;
Salas, S ;
Eysteries, S ;
Nasser, V ;
Finetti, P ;
Ginestier, C ;
Charafe-Jauffret, E ;
Loriod, B ;
Bachelart, L ;
Montfort, J ;
Victorero, G ;
Viret, F ;
Ollendorff, V ;
Fert, V ;
Giovaninni, M ;
Delpero, JR ;
Nguyen, C ;
Viens, P ;
Monges, G ;
Birnbaum, D ;
Houlgatte, R .
ONCOGENE, 2004, 23 (07) :1377-1391
[4]
Boland CR, 1998, CANCER RES, V58, P5248
[5]
ENHANCED MOTILITY IN NIH-3T3 FIBROBLASTS THAT OVEREXPRESS GELSOLIN [J].
CUNNINGHAM, CC ;
STOSSEL, TP ;
KWIATKOWSKI, DJ .
SCIENCE, 1991, 251 (4998) :1233-1236
[6]
Gelsolin-induced epithelial cell invasion is dependent on Ras-Rac signaling [J].
De Corte, V ;
Bruyneel, E ;
Boucherie, C ;
Mareel, M ;
Vandekerckhove, J ;
Gettemans, J .
EMBO JOURNAL, 2002, 21 (24) :6781-6790
[7]
The transcription factor snail induces tumor cell invasion through modulation of the epithelial cell differentiation program [J].
De Craene, B ;
Gilbert, B ;
Stove, C ;
Bruyneel, E ;
van Roy, F ;
Berx, G .
CANCER RESEARCH, 2005, 65 (14) :6237-6244
[8]
Dong Y, 1999, INT J CANCER, V81, P930, DOI 10.1002/(SICI)1097-0215(19990611)81:6<930::AID-IJC15>3.0.CO
[9]
2-A
[10]
Actin binding proteins: Regulation of cytoskeletal microfilaments [J].
Dos Remedios, CG ;
Chhabra, D ;
Kekic, M ;
Dedova, IV ;
Tsubakihara, M ;
Berry, DA ;
Nosworthy, NJ .
PHYSIOLOGICAL REVIEWS, 2003, 83 (02) :433-473