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PMID: 1359533 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction.

Peinado MA, Malkhosyan S, Velazquez A, Perucho M

Abstract

The arbitrarily primed polymerase chain reaction (AP-PCR) [Welsh, J. & McClelland, M. (1990) Nucleic Acids Res. 18, 7213-7218] has been used to detect somatic genetic alterations in tumors of the colon and rectum. DNA fingerprints generated by single arbitrary primers were compared between normal and tumor tissue of the same individuals. AP-PCR bands showing decreased and increased intensities in tumor tissue DNA, relative to normal, have been cloned after reamplification with the same arbitrary primer. Standard restriction fragment length polymorphism and Southern blot analyses show that these DNA sequences have undergone allelic losses and gains, respectively, in the tumor cell genome. The deleted sequences have been assigned to the short arm of chromosome 17 by PCR of somatic hamster/human cell hybrids and linkage analysis. These results show the ability of the AP-PCR to detect and isolate, in a single step, DNA sequences representing two of the genetic alterations that underlie the aneuploidy of cancer cells: losses of heterozygosity and chromosomal gains. Altogether, they also show the quantitative nature of the amplification levels obtained in vitro by AP-PCR, which thus provides the basis for an alternative molecular approach to cancer cytogenetics.

MeSH Terms
Adenocarcinoma/genetics Adenoma/genetics Alleles Base Sequence Blotting, Southern Chromosomes, Human, Pair 17 Colonic Neoplasms/genetics DNA Fingerprinting DNA, Neoplasm/genetics,isolation & purification Humans Liver Neoplasms/genetics,secondary Molecular Sequence Data Oligodeoxyribonucleotides Polymerase Chain Reaction/methods Polymorphism, Restriction Fragment Length Rectal Neoplasms/genetics Restriction Mapping Sequence Deletion
Chemicals
DNA, Neoplasm Oligodeoxyribonucleotides
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Peinado M A
California Institute of Biological Research, La Jolla 92037.
Malkhosyan S
Velazquez A
Perucho M
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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
1992-11-01
Pages
10065-9
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC50278
Subset
IM
Grants
NCI NIH HHS · CA 33021 · United States
NCI NIH HHS · CA 38579 · United States
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