Label-Free Quantitative Proteomics and N-terminal Analysis of Human Metastatic Lung Cancer Cells |
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Authors: | Hophil Min Dohyun Han Yikwon Kim Jee Yeon Cho Jonghwa Jin Youngsoo Kim |
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Institution: | 1.Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 110-799, Korea;2.Institute of Medical and Biological Engineering, Medical Research Center, Seoul National University College of Medicine, Seoul 110-799, Korea;3.Division of Life Sciences and Biotechnology, Korea University, Seoul 136-701, Korea |
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Abstract: | Proteomic analysis is helpful in identifying cancer-associated proteins that are differentially expressed and fragmented that can be annotated as dysregulated networks and pathways during metastasis. To examine meta-static process in lung cancer, we performed a proteomics study by label-free quantitative analysis and N-terminal analysis in 2 human non-small-cell lung cancer cell lines with disparate metastatic potentials—NCI-H1703 (primary cell, stage I) and NCI-H1755 (metastatic cell, stage IV). We identified 2130 proteins, 1355 of which were common to both cell lines. In the label-free quantitative analysis, we used the NSAF normalization method, resulting in 242 differential expressed proteins. For the N-terminal proteome analysis, 325 N-terminal peptides, including 45 novel fragments, were identified in the 2 cell lines. Based on two proteomic analysis, 11 quantitatively expressed proteins and 8 N-terminal peptides were enriched for the focal adhesion pathway. Most proteins from the quantitative analysis were upregulated in metastatic cancer cells, whereas novel fragment of CRKL was detected only in primary cancer cells. This study increases our understanding of the NSCLC metastasis proteome. |
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Keywords: | label-free quantitative analysis metastasis N-terminal analysis non-small-cell lung cancer |
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