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Identification and chromosome mapping of loci predisposing to colorectal cancer that control Wnt/ß-catenin pathway and progression of early lesions in the rat

De Miglio, Maria Rosaria and Virdis, Patrizia and Calvisi, Diego Francesco and Mele, Daniela and Muroni, Maria Rosaria and Frau, Maddalena and Pinna, Federico and Tomasi, Maria Lauda and Simile, Maria Maddalena and Pascale, Rosa Maria and Feo, Francesco (2007) Identification and chromosome mapping of loci predisposing to colorectal cancer that control Wnt/ß-catenin pathway and progression of early lesions in the rat. Carcinogenesis, Vol. 28 (11), p. 2367-2374. ISSN 1460-2180. Article.

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DOI: 10.1093/carcin/bgm119

Abstract

Sporadic colorectal cancer (CRC) is a major health concern worldwide. Epidemiologic evidence suggests a polygenic predisposition to CRC, but the genes responsible remain unknown. Here, we performed genome-wide scanning of male (ACI/SegHsd x Wistar-Furth)F2 (AWF2) rats to map susceptibility genes influencing the evolution of early colorectal lesions to adenocarcinoma following 1,2-dimethylhydrazine administration. Phenotypic analysis revealed higher incidence/multiplicity and lower size of adenomas in ACI/SegHsd (ACI) and (ACI/SegHsd x Wistar-Furth)F1 (AWF1) than Wistar-Furth (WF) rats and higher incidence/multiplicity of poorly differentiated adenocarcinomas in WF than ACI rats, with intermediate values in AWF1 rats. Linkage analysis of 138 AWF2 rats identified three loci on chromosomes 4, 15 and 18 in significant linkage with lesion multiplicity that were identified as rat Colon cancer resistance (rCcr) 1, rCcr2 and rCcr3, respectively. Seven other loci on chromosomes 5, 6, 15, 17, 18 and 20 were in suggestive linkage with adenoma/adenocarcinoma multiplicity/surface area. Six of them were identified as rCcr49 and a locus on chromosome 5 was identified as a susceptibility locus, rCcs1. Significant interactions between rCcr3 and rCcr6, rCcr6 and rCcr8 and rCcr5 and rCcr9, and four novel epistatic loci controlling multiplicity/size of colorectal lesions were discovered. Apc, located at rCcr3, did not show functional promoter polymorphisms. However, influence of susceptibility/resistance genes on Wnt/ß-catenin pathway was shown by defective ß-catenin inactivation in WF but not in ACI and AWF1 rat adenocarcinomas. These data indicate that inheritance of predisposition to CRC depends on interplays of several genetic factors, and suggest a possible mechanism of polygenic control of CRC progression.

Item Type:Article
ID Code:4319
Status:Published
Refereed:Yes
Uncontrolled Keywords:Sporadic colorectal cancer (CRC), adenocarcinoma, AWF1 rats
Subjects:Area 06 - Scienze mediche > MED/04 Patologia generale
Divisions:001 Università di Sassari > 01 Dipartimenti > Scienze biomediche
Publisher:Oxford University Press
ISSN:1460-2180
Copyright Holders:© The Author 2007
Deposited On:20 Aug 2010 13:18

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