Microsatellite instability of each tumor in sporadic synchronous multiple colorectal cancers

Citation
Y. Abe et al., Microsatellite instability of each tumor in sporadic synchronous multiple colorectal cancers, ONCOL REP, 8(2), 2001, pp. 299-304
Citations number
28
Categorie Soggetti
Oncology
Journal title
ONCOLOGY REPORTS
ISSN journal
1021335X → ACNP
Volume
8
Issue
2
Year of publication
2001
Pages
299 - 304
Database
ISI
SICI code
1021-335X(200103/04)8:2<299:MIOETI>2.0.ZU;2-7
Abstract
The purpose of this study was to elucidate microsatellite instability (MSI) and p53 expression for each tumor in cases with sporadic synchronous multi ple colorectal cancers. Twenty-nine patients with sporadic synchronous mult iple colorectal cancer were examined. There were sixty-five tumors, all of which indicated adenocarcinoma histopathologically. The MSI was assessed us ing six microsatellite markers (BAT26, BAT40, D2S136, D5S346, D11S922, D17S 250). Tumors with two or more positive loci were determined to be MSI-H (hi gh-frequency MSI), tumors with one positive locus were designated as MSI-L (low-frequency MSI) and tumors lacking apparent instability were designated as MSS (microsatellite stable). In addition, overexpression of p53 protein was examined using immunohistochemical (IHC) methods for each tumor. The D O-7 monoclonal antibody was used in the IHC assessments. The following resu lts were obtained: i) there were nine patients who indicated MSI-H at the f irst tumor (1-H group) and 20 patients who had MSI-L or MSS at the first tu mor (1-LS group). ii) The ratio of cases that indicated MSI-H at the second tumor and beyond in the 1-H group was 88.9% (8/9), which was significantly higher than that of the 1-LS group (30.0%, 6/20) (p=0.0021). iii) The freq uency of cases with the right-sided colon in the 1-H group (61.9%) was sign ificantly higher than that of the 1-LS group (27.3%) (p=0.0073). In additio n, a significant difference was noted in terms of the ratio of cases with p oorly differentiated adenocarcinoma or mucinous carcinoma between the two g roups [1-H group (19.0%) vs 1-LS group (0%), p=0.0028]. Furthermore, no dis tinct relationship between MSI status and p53 overexpression was obtained. In conclusion, we think that sporadic synchronous multiple colorectal cance rs should be divided into two types; one type that indicates multiple occur rence of MSI-H consecutive tumors and another type that shows multiple occu rrence irrespective of MSI.