Proceedings of the National Academy of Sciences · 1990 · 259 citations · 45 references
MedicineMolecular BiologyOncologyCancer GeneticsGastrointestinal OncologyMolecular OncologyCancer GenomicsGastric CancerGrowth Factor Receptor OncogenesGrowth Factor SignalingCancer Cell Line ModelsGastric Cancer GeneticsHeparin-binding Proteins
DNA fragments amplified in a stomach cancer-derived cell line, KATO-III, were previously identified by the in-gel DNA renaturation method, and a 0.2-kilobase-pair fragment of the amplified sequence was subsequently cloned. By genomic walking, a portion of the exon of the gene flanking this 0.2-kilobase-pair fragment was cloned, and the gene was designated as K-sam (KATO-III cell-derived stomach cancer amplified gene). The K-sam cDNAs, corresponding to the 3.5-kilobase K-sam mRNA, were cloned from the KATO-III cells. Sequence analysis revealed that this gene coded for 682 amino acid residues that satisfied the characteristics of the receptor tyrosine kinase. The K-sam gene had significant homologies with bek, FLG, and chicken basic fibroblast growth factor receptor gene. The K-sam gene was amplified in KATO-III cells with the major transcript of 3.5-kilobases in size. This gene was also expressed in some other stomach cancer cells, a small cell lung cancer, and germ cell tumors.
45
Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
Randall K. Saiki, David H. Gelfand, Susanne Stoffel et al. · Science · 1988 · 17.2K citations
A simple and very efficient method for generating cDNA libraries
Ueli Gubler, Beth J. Hoffman · Gene · 1983 · 4.6K citations