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Degenerate Oligonucleotide Primed-polymerase Chain Reaction-based Array Comparative Genomic Hybridization for Extensive Amplicon Profiling of Breast Cancers : a New Approach for the Molecular Analysis of Paraffin-embedded Cancer Tissue

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 2001 May 5
PMID 11337360
Citations 20
Authors
Affiliations
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Abstract

We have developed a protocol for degenerate oligonucleotide-primed-polymerase chain reaction-based array comparative genomic hybridization (array CGH) that, when combined with a laser microdissection technique, allows the analysis of cancer cell populations isolated from routine, formalin-fixed, paraffin-embedded tissue samples. Comparison of copy number changes detected by degenerate oligonucleotide-primed-polymerase chain reaction-based array CGH to those detected by conventional array CGH or fluorescence in situ hybridization, demonstrated that amplifications can be reliably detected. Using a genomic microarray containing 57 oncogenes, we screened a total of 28 breast cancer samples and obtained a detailed amplicon profile that is the most comprehensive to date in human breast cancer. The array CGH method described here will allow the genetic analysis of paraffin-embedded human cancer materials for example in the context of clinical trials.

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References
1.
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D . High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet. 1998; 20(2):207-11. DOI: 10.1038/2524. View

2.
Mohapatra G, Moore D, Kim D, Grewal L, Hyun W, Waldman F . Analyses of brain tumor cell lines confirm a simple model of relationships among fluorescence in situ hybridization, DNA index, and comparative genomic hybridization. Genes Chromosomes Cancer. 1997; 20(4):311-9. DOI: 10.1002/(sici)1098-2264(199712)20:4<311::aid-gcc1>3.0.co;2-4. View

3.
Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T . Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer. 1997; 20(4):399-407. View

4.
Davidson J, Gorringe K, Chin S, Orsetti B, Besret C, Courtay-Cahen C . Molecular cytogenetic analysis of breast cancer cell lines. Br J Cancer. 2000; 83(10):1309-17. PMC: 2408781. DOI: 10.1054/bjoc.2000.1458. View

5.
Telenius H, Carter N, Bebb C, Nordenskjold M, Ponder B, Tunnacliffe A . Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics. 1992; 13(3):718-25. DOI: 10.1016/0888-7543(92)90147-k. View