K-ras mutation detection by hybridization to a polypyrrole DNA chip

被引:0
|
作者
Lopez-Crapez, E
Livache, T
Marchand, J
Grenier, J
机构
[1] Ctr Rech Cancerol, CLRC Val dAurelle Paul Lamarque, F-34298 Montpellier 5, France
[2] CIS Bio Int, F-91192 Gif Sur Yvette, France
关键词
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暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Detection of mutations in cancer-related genes is of major importance for both basic knowledge and clinical practice. Several strategies have been developed to diagnose these alterations. We describe a method based on polypyrrole DNA chip technology to detect K-ras gene mutations in tumors. Methods: An oligodeoxynucleotide array was constructed on a silicon device by copolymerization of 5'-pyrrole-labeled oligodeoxynucleotides and pyrrole. The samples to be analyzed were then amplified by PCR, and the single-stranded biotin-labeled amplified DNA was specifically hybridized to the addressed probes. Perfectly matched duplexes were detected by fluorescence microscopy using R-phycoerythrin as the detection label. The developed methodology was applied to genotype assignment of K-ras in human samples. The genotypes of 75 DNA genomic samples from colorectal cancer patients were analyzed side by side using direct DNA sequencing and a polypyrrole DNA chip. Results: The chip method unequivocally defined all of the genotypes. Mutations present at <10% of the wild-type DNA concentration could be distinguished. Conclusions: This probe array assay is a rapid and reliable procedure that may be used to detect mutations. (C) 2001 American Association for Clinical Chemistry.
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收藏
页码:186 / 194
页数:9
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