| Analysis of secreted proteins for the study of bladder cancer cell aggressiveness. | |
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MedLine Citation:
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PMID: 20423150 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Secreted proteins play a key role in cell signaling, communication, and migration. We recently described the development of an aggressive variant (T24M) of the bladder cancer cell line T24. Using this cell line model, the objective of our work was the identification of secreted proteins involved in the acquisition of the aggressive phenotype. Using in vitro assays, we demonstrate that conditioned media of the T24M cells promote motility of the parental less aggressive T24 cells. Proteomic analysis of cell culture conditioned media by the use of 2-dimensional gel electrophoresis coupled to MALDI TOF MS and LC-MS approaches resulted in enrichment and detection of multiple classical extracellular and secreted proteins such as fibronectin, cystatin, fibrillin, fibulin, interleukin 6, etc. Comparison of the secretome of the T24 and T24M cells indicated differences in proteins with potential involvement in the mechanisms of cell aggressiveness including SPARC, tPA, and clusterin. These findings were further confirmed by Western blot analysis. In the case of SPARC, further studies involving transwell assays indicated that blockage of the protein in the presence of SPARC-specific Abs results in decreased cell motility. Collectively, our study provides a 2DE-based comprehensive analysis of bladder cancer cell secretome. The results indicate various secreted proteins with potential involvement in bladder cancer cell aggressiveness and more specifically provide initial evidence for special role of SPARC in bladder cancer cell motility and invasiveness. |
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Authors:
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Manousos Makridakis; Maria G Roubelakis; Vasiliki Bitsika; Veronica Dimuccio; Martina Samiotaki; Sophia Kossida; George Panayotou; Jonathan Coleman; Giovanni Candiano; Nikolaos P Anagnou; Antonia Vlahou |
Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Journal of proteome research Volume: 9 ISSN: 1535-3907 ISO Abbreviation: J. Proteome Res. Publication Date: 2010 Jun |
Date Detail:
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Created Date: 2010-08-16 Completed Date: 2010-11-22 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101128775 Medline TA: J Proteome Res Country: United States |
Other Details:
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Languages: eng Pagination: 3243-59 Citation Subset: IM |
Affiliation:
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Biotechnology Division, Biomedical Research Foundation, Academy of Athens, Athens, Greece. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Cell Line, Tumor Cell Movement / physiology Electrophoresis, Gel, Two-Dimensional Humans Immunohistochemistry Neoplasm Invasiveness Neoplasm Proteins / chemistry, secretion* Osteonectin / chemistry, secretion Proteome / chemistry, secretion* Proteomics Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Tumor Markers, Biological / chemistry, secretion* Urinary Bladder Neoplasms / pathology, secretion* |
| Chemical | |
Reg. No./Substance:
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0/Neoplasm Proteins; 0/Osteonectin; 0/Proteome; 0/Tumor Markers, Biological |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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