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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1997-5-12
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pubmed:abstractText |
Mutations in the K-ras gene are often identified in lung tumors and are implicated in the development of lung cancer. We used a sensitive method to analyze low-fraction mutations occurring in codon 12 of the K-ras gene in 114 primary lung tumors, including 77 adenocarcinomas, 31 squamous cell carcinomas and 6 adenosquamous carcinomas, which had previously been shown to be negative for codon 12 K-ras mutation in a first screening using less sensitive methods. Sixteen of these tumors were found to contain a low-fraction mutation, including 9 mutations among the adenocarcinomas, six mutations among the squamous cell carcinomas and one mutation among the adenosquamous carcinomas. Our study also showed that the occurrence of low-fraction mutation was associated with a positive smoking history, as was previously found for the occurrence of high-fraction mutation. Patients with low-fraction mutations were younger (mean age 58.8 years) than those with either high-fraction mutations (63.2 years) or no mutation (66 years). Patients with low-fraction mutations were more often stage 1 (8 of 10) than patients with either high fraction mutations (22 of 44) or no mutation (33 of 71). Moreover, the overall survival was better for the group with a low-fraction mutation than both the high-fraction mutation group and the group with no K-ras mutation, but due to small sample size, the difference was not statistically significant. Our results suggest that using highly sensitive methods of K-ras mutant detection in tumor DNA could obscure differences between patients in whom the mutation is found throughout the tumor, those in whom the mutation is only present in a small subpopulation and those who have no mutation.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
74
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
162-70
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9133449-Adenocarcinoma,
pubmed-meshheading:9133449-Aged,
pubmed-meshheading:9133449-Carcinoma, Adenosquamous,
pubmed-meshheading:9133449-Carcinoma, Squamous Cell,
pubmed-meshheading:9133449-Codon,
pubmed-meshheading:9133449-Electrophoresis,
pubmed-meshheading:9133449-Female,
pubmed-meshheading:9133449-Genes, ras,
pubmed-meshheading:9133449-Humans,
pubmed-meshheading:9133449-Lung Neoplasms,
pubmed-meshheading:9133449-Male,
pubmed-meshheading:9133449-Middle Aged,
pubmed-meshheading:9133449-Mutation,
pubmed-meshheading:9133449-Polymerase Chain Reaction,
pubmed-meshheading:9133449-Sensitivity and Specificity
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pubmed:year |
1997
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pubmed:articleTitle |
Detection of low-fraction K-ras mutations in primary lung tumors using a sensitive method.
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pubmed:affiliation |
Department of Environmental and Occupational Health, University of Pittsburgh, PA 15238, USA. pho1.vms.cis.pitt.edu.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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