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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Loss of heterozygosity at chromosomes 3p and 17p in primary non-small cell lung cancer.

BACKGROUND: Loss of heterozygosity (LOH) of selected regions at chromosomes 3p and 17p in non-small cell lung cancer (NSCLC) and the association of these abnormalities with major clinical parameters and prognosis were studied. MATERIALS AND METHODS: The study group included 92 consecutive primary NSCLC tumours and four microsatellite markers from chromosome 3p and three markers from 17p were analyzed. RESULTS: LOH of at least one locus was found in 83% of all analyzed tumours. Most frequently deletion (58%) was found at locus D3S1481 (3p14.2). Sequence deletions of D17S520 (17p12) and TP53 (17p13.1) occurred in 52% of tumours. LOH occurrence at 3p and 17p was more frequent in squamous cell carcinomas compared to adenocarcinomas (89% vs. 75%), but this difference was not significant. CONCLUSION: No significant association was found between LOH on any analyzed loci and tumour stage ( TNM) and grade (G). There was no correlation between LOH and survival.[1]

References

  1. Loss of heterozygosity at chromosomes 3p and 17p in primary non-small cell lung cancer. Chmara, M., Wozniak, A., Ochman, K., Kobierska, G., Dziadziuszko, R., Sosinska-Mielcarek, K., Jassem, E., Skokowski, J., Jassem, J., Limon, J. Anticancer Res. (2004) [Pubmed]
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