Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System

To investigate the ability of an automated fluorescent analyzing system to detect microsatellite alterations, in patients with bladder cancer. We investigated 11 with pathology proven bladder Transitional Cell Carcinoma (TCC) for microsatellite alterations in blood, urine, and tumor biopsies. DNA wa...

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Main Authors: Sarel Halachmi, Michal Cohen, Raymond Szargel, Nadin Cohen
Format: Article
Language:English
Published: Hindawi Limited 2007-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2007.176
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spelling doaj-02101eaa0d5a48a786e8f90c464397e52020-11-25T01:37:59ZengHindawi LimitedThe Scientific World Journal1537-744X2007-01-0171553155710.1100/tsw.2007.176Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing SystemSarel Halachmi0Michal Cohen1Raymond Szargel2Nadin Cohen3The Department of Urology Rambam Medical Center, Haifa, IsraelThe Department of Genetics, Tamkin Human Molecular Genetics Research Facility, Faculty of Medicine, Technion Israeli Institute of Technology, Haifa, IsraelThe Department of Genetics, Tamkin Human Molecular Genetics Research Facility, Faculty of Medicine, Technion Israeli Institute of Technology, Haifa, IsraelThe Department of Genetics, Tamkin Human Molecular Genetics Research Facility, Faculty of Medicine, Technion Israeli Institute of Technology, Haifa, IsraelTo investigate the ability of an automated fluorescent analyzing system to detect microsatellite alterations, in patients with bladder cancer. We investigated 11 with pathology proven bladder Transitional Cell Carcinoma (TCC) for microsatellite alterations in blood, urine, and tumor biopsies. DNA was prepared by standard methods from blood, urine and resected tumor specimens, and was used for microsatellite analysis. After the primers were fluorescent labeled, amplification of the DNA was performed with PCR. The PCR products were placed into the automated genetic analyser (ABI Prism 310, Perkin Elmer, USA) and were subjected to fluorescent scanning with argon ion laser beams. The fluorescent signal intensity measured by the genetic analyzer measured the product size in terms of base pairs. We found loss of heterozygocity (LOH) or microsatellite alterations (a loss or gain of nucleotides, which alter the original normal locus size) in all the patients by using fluorescent microsatellite analysis and an automated analyzing system. In each case the genetic changes found in urine samples were identical to those found in the resected tumor sample. The studies demonstrated the ability to detect bladder tumor non-invasively by fluorescent microsatellite analysis of urine samples. Our study supports the worldwide trend for the search of non-invasive methods to detect bladder cancer. We have overcome major obstacles that prevented the clinical use of an experimental system. With our new tested system microsatellite analysis can be done cheaper, faster, easier and with higher scientific accuracy.http://dx.doi.org/10.1100/tsw.2007.176
collection DOAJ
language English
format Article
sources DOAJ
author Sarel Halachmi
Michal Cohen
Raymond Szargel
Nadin Cohen
spellingShingle Sarel Halachmi
Michal Cohen
Raymond Szargel
Nadin Cohen
Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System
The Scientific World Journal
author_facet Sarel Halachmi
Michal Cohen
Raymond Szargel
Nadin Cohen
author_sort Sarel Halachmi
title Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System
title_short Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System
title_full Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System
title_fullStr Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System
title_full_unstemmed Molecular Detection of Bladder Cancer by Fluorescence Microsatellite Analysis and an Automated Genetic Analyzing System
title_sort molecular detection of bladder cancer by fluorescence microsatellite analysis and an automated genetic analyzing system
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2007-01-01
description To investigate the ability of an automated fluorescent analyzing system to detect microsatellite alterations, in patients with bladder cancer. We investigated 11 with pathology proven bladder Transitional Cell Carcinoma (TCC) for microsatellite alterations in blood, urine, and tumor biopsies. DNA was prepared by standard methods from blood, urine and resected tumor specimens, and was used for microsatellite analysis. After the primers were fluorescent labeled, amplification of the DNA was performed with PCR. The PCR products were placed into the automated genetic analyser (ABI Prism 310, Perkin Elmer, USA) and were subjected to fluorescent scanning with argon ion laser beams. The fluorescent signal intensity measured by the genetic analyzer measured the product size in terms of base pairs. We found loss of heterozygocity (LOH) or microsatellite alterations (a loss or gain of nucleotides, which alter the original normal locus size) in all the patients by using fluorescent microsatellite analysis and an automated analyzing system. In each case the genetic changes found in urine samples were identical to those found in the resected tumor sample. The studies demonstrated the ability to detect bladder tumor non-invasively by fluorescent microsatellite analysis of urine samples. Our study supports the worldwide trend for the search of non-invasive methods to detect bladder cancer. We have overcome major obstacles that prevented the clinical use of an experimental system. With our new tested system microsatellite analysis can be done cheaper, faster, easier and with higher scientific accuracy.
url http://dx.doi.org/10.1100/tsw.2007.176
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