Source:http://linkedlifedata.com/resource/pubmed/id/12527710
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2003-1-15
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pubmed:abstractText |
Stage I non-small cell carcinoma (NSCLC) of the lung is typically treated with surgery alone, but with a 30 to 40% recurrence rate. Prognostic factors to stratify these patients into high- and low-risk groups would be of significant clinical value, but published data are conflicting. We studied 39 Stage I NSCLC treated with resection alone, followed for a minimum of 5 years, and divided into recurrent (RC) and non-recurrent (NRC) groups (n = 12 and 27, respectively). Allelic imbalance (loss of heterozygosity, LOH) involving genomic regions containing L-myc (1p32), hOGG1 (3p26), APC/MCC (5q21), c-fms (5q33.3), p53 (17p13), and DCC (18q21), and point mutational change in K-ras-2 (12p12) were studied by PCR-based microsatellite analysis and DNA sequencing. Mutations in k-ras-2 were seen in 25% and 19% of RC and NRC tumors, respectively, most frequently in adenocarcinomas. LOH in the RC and NRC respectively were 50% and 37% for L-myc, 60% and 33% for hOGG1, 60% and 50% for APC, 38% and 35% for c-fms, 78% and 75% for p53, and 17% and 45% for DCC. No statistical significance was seen comparing any of the allelic alterations with recurrence. LOH for hOGG1 and L-myc were more commonly seen in squamous cell carcinomas. Stage I NSCLC are genetically heterogeneous with respect to mutation acquisition. The approach of investigating a panel of genes for alterations can be applied to any given tumor type, and provides information on patterns of mutations/LOH that can help us better understand the molecular biology of tumorigenesis.
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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 |
Jan
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pubmed:issn |
0893-3952
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
28-34
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12527710-Aged,
pubmed-meshheading:12527710-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:12527710-DNA, Neoplasm,
pubmed-meshheading:12527710-Female,
pubmed-meshheading:12527710-Genes, ras,
pubmed-meshheading:12527710-Humans,
pubmed-meshheading:12527710-Loss of Heterozygosity,
pubmed-meshheading:12527710-Lung Neoplasms,
pubmed-meshheading:12527710-Male,
pubmed-meshheading:12527710-Middle Aged,
pubmed-meshheading:12527710-Mutation,
pubmed-meshheading:12527710-Neoplasm Recurrence, Local,
pubmed-meshheading:12527710-Neoplasm Staging,
pubmed-meshheading:12527710-Polymerase Chain Reaction,
pubmed-meshheading:12527710-Predictive Value of Tests,
pubmed-meshheading:12527710-Prognosis
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pubmed:year |
2003
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pubmed:articleTitle |
Widespread molecular alterations present in stage I non-small cell lung carcinoma fail to predict tumor recurrence.
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pubmed:affiliation |
Department of Pathology, University of Pittsburgh Medical Center, Presbyterian University Hospital, Pittsburgh, Pennsylvania 15213, USA.
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pubmed:publicationType |
Journal Article
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