The reproducibility of microsatellite instability from different regions of the same sporadic colon cancer has not been addressed. We therefore microdissected and extracted DNA from three to nine separate regions of 13 highly unstable sporadic colon cancers. Each region was then evaluated by polymer
Microsatellite instability in sporadic human breast cancers
β Scribed by Tatsuya Toyama; Hirotaka Iwase; Hiroko Yamashita; Hiroji Iwata; Toshinari Yamashita; Kazuko Ito; Yasuo Hara; Mariko Suchi; Taiji Kato; Takaaki Nakamura; Shunzo Kobayashi
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- French
- Weight
- 486 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Human breast-cancer specimens from 100 patients were analyzed for microsatellite instability (referred to as replication error; RER) at I 2 genomic loci on 7 chromosomes, and results were correlated with clinicopathologic characteristics. In 42 of I00 breast-cancer patients, we investigated whether RER was associated with the amplification of oncogenes and/or suppmsion of tumor-suppressor genes. Of the 100 patients, 8 (8%) were RER-positive at one or more chromosomal loci. The majority of RER-positive patients had early-stage disease with ER-positive tumors, suggesting that RER occurs early in breast tumorigenesis. However, no significant correlation was observed between RER and oncogenes or tumor-suppressor genes. Thus, the mechanism of RER in sporadic human breast cancer may be independent of the multi-step minogenesis caused by the alterations of oncogenes and tumor-suppressor genes.
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