Project/Area Number |
14570160
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Human pathology
|
Research Institution | Kitasato University |
Principal Investigator |
OKAYASU Isao Kitasato University School of Medicine, Department of Pathology, Professor, 医学部, 教授 (20014342)
|
Co-Investigator(Kenkyū-buntansha) |
YOSHIDA Tsutomu Kitasato University School of Medicine, Department of Pathology, Assistant Professor, 医学部, 講師 (90316943)
|
Project Period (FY) |
2002 – 2003
|
Project Status |
Completed (Fiscal Year 2003)
|
Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2002: ¥2,300,000 (Direct Cost: ¥2,300,000)
|
Keywords | ulcerative colitis / carcinogenesis / genetic instability / stromal cell / microdissection / microsatellite instability / colon cancer / chronic inflammation / Microdissection |
Research Abstract |
To know roles of genetic instability of stromal cells on carcinogenesis in ulcerative colitis (UC), microsatellite instability (MSI) and loss of heterozygosity (LOH) were investigated in epithelial and stromal cells separated by microdissection, by using PCR-SSCP method. In sporadic colon cancers, MSI positive results were obtained for both epithelium and stromal tissue. While MSI in epithelium correlated with differentiation and Dukes' stage, that in stroma demonstrated an inverse correlation, being particularly frequent in well differentiated adenocarcinomas and Dukes' A lesions, suggesting an alternative pathway of carcinogenesis involving stromal genetic instability in the development of colon cancers. In contrast, although chromosome 17-MSI and -LOH in epithelium correlated with histological progression, in stroma they showed a consistently high frequency throughout the different stages, indicating a distinct carcinogenesis pathway of UC.
|