【摘 要】
:
We used a functional genomic approach that integrated simultaneous genomic and transcript microarray, proteomics, and tissue microarray analyses to directly
【机 构】
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Department of Pathology University of Maryland School of Medicine USA
【出 处】
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BIT Life Sciences' 1st Annual World Cancer Congess-2008(
论文部分内容阅读
We used a functional genomic approach that integrated simultaneous genomic and transcript microarray, proteomics, and tissue microarray analyses to directly identify putative oncogenes in lung tumorigenesis.We first identified 183 genes with increases in both genomic copy number and transcript in six lung cancer cell lines.Next, we used two-dimensional polyacrylamide gel electrophoresis and mass spectrometry to identify 42 proteins that were overexpressed in the cancer cells relative to normal cells.Comparing the genes with the proteins, we identified four genes-PRDX1, EEF1A2, CALR, and 14-3-3zeta in which elevated protein expression correlated with both increased DNA copy number and increased transcript levels.
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