Microsatellite instability in sporadic human breast cancers. Int J Cancer 1996 Nov 15;68(4):447-51
Date
11/15/1996Pubmed ID
8945614DOI
10.1002/(SICI)1097-0215(19961115)68:4<447::AID-IJC8>3.0.CO;2-0Scopus ID
2-s2.0-0029658742 (requires institutional sign-in at Scopus site) 54 CitationsAbstract
Human breast-cancer specimens from 100 patients were analyzed for microsatellite instability (referred to as replication error; RER) at 12 genomic loci on 7 chromosomes, and results were correlated with clinicopathologic characteristics. In 42 of 100 breast-cancer patients, we investigated whether RER was associated with the amplification of oncogenes and/or suppression 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 carcinogenesis caused by the alterations of oncogenes and tumor-suppressor genes.
Author List
Toyama T, Iwase H, Yamashita H, Iwata H, Yamashita T, Ito K, Hara Y, Suchi M, Kato T, Nakamura T, Kobayashi SAuthor
Mariko Suchi MD, PhD Professor in the Pathology department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
Breast NeoplasmsDNA Repair
Female
Genes, Tumor Suppressor
Humans
Microsatellite Repeats
Middle Aged
Oncogenes