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LIU Gui-zhi, WU Yi-ming. Differential Analysis of Two-dimension Gel Electrophoresis Profiles of Human Early-stage Lung Adenocarcinoma and Tumor-adjacent Tissue[J]. Cancer Research on Prevention and Treatment, 2008, 35(08): 551-554. DOI: 10.3971/j.issn.1000-8578.1284
Citation: LIU Gui-zhi, WU Yi-ming. Differential Analysis of Two-dimension Gel Electrophoresis Profiles of Human Early-stage Lung Adenocarcinoma and Tumor-adjacent Tissue[J]. Cancer Research on Prevention and Treatment, 2008, 35(08): 551-554. DOI: 10.3971/j.issn.1000-8578.1284

Differential Analysis of Two-dimension Gel Electrophoresis Profiles of Human Early-stage Lung Adenocarcinoma and Tumor-adjacent Tissue

  • Objective To screen and identify differential expression proteins,and to obtain theoretical data for studying human stage Ⅰ lung adenocarcinoma molecular mechanism and finding early biomarker. Methods The total proteins of 12 human stage Ⅰ lung adenocarcinoma tissue and normal tumor-adjacent tissue were separated,using 170mm long immobilized pH gradient(IPG) gel strips,pH3-10,for the first dimension and homogeneous SDS-polyacrylamide gel electrophoresis(SDS-PAGE)(12%T) for the second dimension.The differen expression proteins were analyzed with PDQuest image analysis sof tware, then identified using mat rix-assisted laser desorption/ ionization time of flight mass spect romet ry (MAL-DI2TOF2MS) and database searching. Results  The well-reproducible -2DE gel patterns of human stage Ⅰlung adenocarcinoma and normal tumor2adjacent tissue were established and 26 differential proteins were screened. Nine of 26 differential protein spot s were cut out f rom the preparation gels and were iden-tified with MALDI-TOF-MS. Comparing with the protein database, four candidate proteins were identified with MS. They were 60S acidic ribosomal protein P2, Cathepsin B precursor, Apolipoprotein A2I precur-sor and La 4. 1 protein. Conclusion  In this study, 2-DE gel images of human stage Ⅰlung adenocarcino-ma and paired normal tumor-adjacent tissue were established successfully, and identified 4 differential pro-teins. These data will be helpful for studying human lung adenocarcinoma molecular mechanism and screening early biomarker.
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