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Detection of genomic instability in lung cancer tissues by random amplified polymorphic DNA analysis
Author(s) -
T. Ong
Publication year - 1998
Publication title -
carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.688
H-Index - 204
eISSN - 1460-2180
pISSN - 0143-3334
DOI - 10.1093/carcin/19.1.233
Subject(s) - genomic dna , genome instability , biology , ethidium bromide , rapd , primer (cosmetics) , carcinogenesis , microbiology and biotechnology , lung cancer , dna , polymerase chain reaction , genetics , cancer , gene duplication , pathology , gene , dna damage , chemistry , population , medicine , environmental health , organic chemistry , genetic diversity
Genomic instability resulting in multiple mutations is believed to be a driving force in the carcinogenic process. In this study, the random amplified polymorphic DNA (RAPD) technique, a simple PCR-based DNA polymorphism assay system, was used for detecting genomic instability in lung cancer tissues. DNAs from 20 lung cancer (18 non-small cell lung cancers and two small cell lung cancers) and their corresponding normal tissues were amplified individually by RAPD with seven different 10-base arbitrary primers. PCR products from RAPD were electrophoretically separated in agarose gels and banding profiles were visualized by ethidium bromide staining. The ability to detect genomic instability in 20 cancer tissues by each single primer ranged from 15 to 75%. DNA changes were detected by at least one primer in 19 (95%) cancer tissues. These results seem to indicate that genomic rearrangement is associated with lung carcinogenesis and that RAPD analysis is useful for the detection of genomic instability in lung cancer tissues.

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