Amplification of cellular oncogenes is an important mechanism of altered gene expression in human
cancers. Using comparative genomic hybridization we recently identified an amplification at 3q26.1-q26.3 in 30% of
squamous cell carcinomas of the lung. A variety of methods including microdissection-mediated procedures permit cloning of genes encoded within amplified domains but do not directly lead to the identification of biologically relevant genes. In this study, we have circumvented this problem by combining an immunological and molecular genetic approach to analyze squamous cell lung
carcinoma. To identify both amplified and
tumor relevant genes, we generated a
cDNA expression library from a
tumor with the 3q amplification and hybridized the expressed recombinant
polypeptides with the autologous serum. Of 400000
cDNA clones we identified 17
antigens which induce an immune response in a patient with squamous cell lung
carcinoma. While most clones represent individual genes sequence analysis revealed that four of the 17 cDNAs are nearly identical with the eukaryotic translation
initiation factor (eIF)-4gamma recently assigned on 3q. We demonstrated that the gene for
eIF-4gamma was amplified within 3q26-q27 in independent squamous cell lung
carcinomas. In this study, we report the identification of several
antigens which elicit an immune response in a squamous cell lung
carcinoma patient including
eIF-4gamma.
eIF-4gamma is encoded by an amplified gene and possibly plays a crucial part in the development of squamous cell lung
carcinoma.