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A frequent deletion of chromosome 5q21 in advanced small cell and non-small cell carcinoma of the lung.
61
Citations
27
References
1994
Year
Gene Deletion DataCytogeneticsGeneticsPathologyAdvanced Small CellTumor BiologyMolecular DiagnosticsChromosome 22Cancer ResearchAdvanced Lung CancerFrequent DeletionChromosome 5Q21MedicineCancer GeneticsCell BiologyLung CancerChromatinCancer GenomicsBronchial NeoplasmChromosome 5Tumor SuppressorOncologyChromosome 9
We have examined the deletion of the long arm of chromosome 5 (5q) in 59 cases of advanced lung cancer [39 cases of small cell lung cancer (SCLC), 20 cases of non-SCLC] using 12 restriction fragment length polymorphism markers on 5q. Of 59 lung cancer cases, 48 (81%) exhibited deletion at any portion of the 5q locus (loci). Such a high frequency of 5q deletion has not been reported in surgically resectable non-SCLC. One SCLC case showed a 5q deletion only in metastatic sites but not in the primary cancer. These data suggest that the inactivation of putative tumor-suppressor gene(s) on 5q may be a late event in the progression of lung cancer. There was no significant difference in frequency of 5q deletion between SCLC and non-SCLC. Compared to non-SCLC, however, SCLC usually showed widespread deletion on 5q. While the most frequent target region was estimated to be about 3-5 megabases at 5q21 around the adenomatous polyposis coli (APC) gene locus, some cases showed more telomeric deletion (5q33-35), suggesting that there are at least two different tumor-suppressor genes on 5q associated with the progression of lung cancer.
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