Literature DB >> 15066319

Accuracy of an array comparative genomic hybridization (CGH) technique in detecting DNA copy number aberrations: comparison with conventional CGH and loss of heterozygosity analysis in prostate cancer.

Seiji Yano1, Hideyasu Matsuyama, Kenji Matsuda, Hiroaki Matsumoto, Satoru Yoshihiro, Katsusuke Naito.   

Abstract

Although genomic DNA microarray (array comparative genomic hybridization [CGH]) technique is a rapid and powerful diagnostic tool for the comprehensive analysis of detailed chromosomal alterations of DNA copy numbers, its accuracy has not been well demonstrated. To clarify the accuracy of this technique, we applied array CGH spotted with 283 specific genes to 11 clinical prostate cancers, and the results were compared with comparative genomic hybridization (conventional CGH) and loss of heterozygosity (LOH) analysis using microsatellite DNA markers. The overall rate of correspondence between array CGH and conventional CGH with respect to the loss of DNA sequences was 94.5%. When the results of both CGH techniques were compared with those of LOH analysis, the correspondence rate of array CGH was significantly higher than that of conventional CGH (93.4% vs. 72.2%, P<0.05). In conclusion, the accuracy of array CGH was higher than that of conventional CGH in detecting losses of the DNA sequences. Array CGH is shown to be a promising tool for screening to identify unknown genes involved in tumorigenesis in prostate cancer.

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Year:  2004        PMID: 15066319     DOI: 10.1016/j.cancergencyto.2003.09.004

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  5 in total

1.  The impact of genomic alterations on the transcriptome: a prostate cancer cell line case study.

Authors:  J Chaudhary; M Schmidt
Journal:  Chromosome Res       Date:  2006-07-12       Impact factor: 5.239

2.  Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis type 1.

Authors:  Seon-Yong Jeong; Sang-Jin Park; Su-Jin Lee; Ho-Jin Park; Hyon J Kim
Journal:  J Korean Med Sci       Date:  2010-04-16       Impact factor: 2.153

3.  The use of whole genome amplification to study chromosomal changes in prostate cancer: insights into genome-wide signature of preneoplasia associated with cancer progression.

Authors:  Simon Hughes; Maisa Yoshimoto; Ben Beheshti; Richard S Houlston; Jeremy A Squire; Andrew Evans
Journal:  BMC Genomics       Date:  2006-03-30       Impact factor: 3.969

4.  Comparison of chromosomal and array-based comparative genomic hybridization for the detection of genomic imbalances in primary prostate carcinomas.

Authors:  Franclim R Ribeiro; Rui Henrique; Merete Hektoen; Marianne Berg; Carmen Jerónimo; Manuel R Teixeira; Ragnhild A Lothe
Journal:  Mol Cancer       Date:  2006-09-04       Impact factor: 27.401

5.  Detection of novel amplicons in prostate cancer by comprehensive genomic profiling of prostate cancer cell lines using oligonucleotide-based arrayCGH.

Authors:  Joern Kamradt; Volker Jung; Kerstin Wahrheit; Laura Tolosi; Joerg Rahnenfuehrer; Martin Schilling; Robert Walker; Sean Davis; Michael Stoeckle; Paul Meltzer; Bernd Wullich
Journal:  PLoS One       Date:  2007-08-22       Impact factor: 3.240

  5 in total

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