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PMID: 11226302 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mechanisms underlying losses of heterozygosity in human colorectal cancers.

Thiagalingam S, Laken S, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B, Lengauer C

Abstract

Losses of heterozygosity are the most common molecular genetic alteration observed in human cancers. However, there have been few systematic studies to understand the mechanism(s) responsible for losses of heterozygosity in such tumors. Here we report a detailed investigation of the five chromosomes lost most frequently in human colorectal cancers. A total of 10,216 determinations were made with 88 microsatellite markers, revealing 245 chromosomal loss events. The mechanisms of loss were remarkably chromosome-specific. Some chromosomes displayed complete loss such as that predicted to result from mitotic nondisjunction. However, more than half of the losses were associated with losses of only part of a chromosome rather than a whole chromosome. Surprisingly, these losses were due largely to structural alterations rather than to mitotic recombination, break-induced replication, or gene conversion, suggesting novel mechanisms for the generation of much of the aneuploidy in this common tumor type.

MeSH Terms
Alleles Chromosome Deletion Colorectal Neoplasms/genetics,pathology Humans In Situ Hybridization, Fluorescence Loss of Heterozygosity Tumor Cells, Cultured
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Thiagalingam S
Oncology Center, Program in Molecular Biology, Johns Hopkins University School of Medicine, 1650 Orleans Street, Baltimore, MD 21231, USA.
Laken S
Willson J K
Markowitz S D
Kinzler K W
Vogelstein B
Lengauer C
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
2001-02-27
Epub
2001-00-13
Pages
2698-702
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC30201
Subset
IM
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