Tumors lacking DNA mismatch repair activity (MMR) from patients with Hereditary Nonpolyposis Colorectal Cancer (HNPCC) or those with sporadic colorectal cancer can be identified by the presence of high levels of instability in repetitive sequences known as microsatellites (MSI). The assessment of MS
A panel of repeat markers for detection of microsatellite instability in murine tumors
โ Scribed by Omar Kabbarah; Mary Ann Mallon; John D. Pfeifer; Winfried Edelmann; Raju Kucherlapati; Paul J. Goodfellow
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 185 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0899-1987
- DOI
- 10.1002/mc.10157
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
A substantial fraction of human malignancies lack functional DNA mismatch repair (MMR), accumulate mutations at high frequency, and exhibit microsatellite instability (MSI). In order to distinguish between MMRโcompetent and MMRโdeficient malignancies, a consensus panel of microsatellite repeats has been adopted for MSI analysis of human tumors. There is no reference panel of repeats for MSI typing of murine malignancies. In this study, we present six new microsatellite repeat markers for MSI typing of mouse tumors. Analysis of polymerase chain reaction (PCR)โamplified tumor DNA from MMRโdeficient and โproficient mice on denaturing polyacrylamide gels revealed that the new panel of microsatellites was more sensitive in detecting MSI than six commonly used CA~n~ repeats. Using the new set of microsatellite markers, we demonstrated the presence of MSI in endometrial carcinoma and cancer precursors from diethylstilbestrol (DES)โtreated mice, pointing to a possible role for loss of MMR in hormonally promoted endometrial tumorigenesis. ยฉ 2003 WileyโLiss, Inc.
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