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pubmed-article:11716502pubmed:abstractTextComparative proteome analysis was performed between human normal (BEAS 2B) and malignant (A549) lung epithelial cells in an attempt to identify novel biomarkers of lung cancer. Approximately 500 protein spots could be separated by mini two-dimensional electrophoresis and visualized with Coomassie blue R-250. Among those relatively abundant proteins, eight spots were changed more than twofold reproducibly and identified by peptide mass fingerprints using mass spectrometry and database search. The increased proteins in A549 were aldehyde dehydrogenase, peroxiredoxin I, fatty acid binding protein, aldoketoreductase, and destrin, whereas the decreased proteins were galectin-1, transgelin, and stathmin. Since human lung is exposed to continuous oxidative stress, antioxidant enzyme peroxiredoxin I was selected for further investigation and its augmented expression was confirmed in cancer tissues compared to normal tissues from lung cancer patients, suggesting peroxiredoxin I as a potential biomarker of lung cancer.lld:pubmed
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pubmed-article:11716502pubmed:authorpubmed-author:LeeJ HJHlld:pubmed
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pubmed-article:11716502pubmed:articleTitleAugmented expression of peroxiredoxin I in lung cancer.lld:pubmed
pubmed-article:11716502pubmed:affiliationDepartment of Life Science, Kwangju Institute of Science and Technology (K-JIST), Kwangju 500-712, Korea.lld:pubmed
pubmed-article:11716502pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11716502pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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