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- PMID: 15274141
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Article: Proteomics of buccal squamous cell carcinoma: The involvement of multiple pathways in tumorigenesis
Title | Proteomics of buccal squamous cell carcinoma: The involvement of multiple pathways in tumorigenesis |
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Authors | |
Keywords | Biomarker Buccal cancer Mass spectronomyi fingerprinting Protein profile Two-dimensional-polyacrylamide get dectrophoresis |
Issue Date | 2004 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics |
Citation | Proteomics, 2004, v. 4 n. 8, p. 2465-2475 How to Cite? |
Abstract | Squamous cell carcinoma (SCC) of the buccal mucosa is an aggressive oral cancer. It mainly occurs in Central and Southeast Asia, and is closely related to the practice of tobacco smoking and betel squid chewing. The high recurrence and low survival rates of buccal SCC require our continued efforts to understand the pathogenesis of the disease for designing better therapeutic strategies. We used proteomic technology to analyze buccal SCC tissues aiming at identifying tumor-associated proteins for the utilization as biomarkers or molecular targets. With the exception of alpha B-crystallin being substantially reduced, a number of proteins were found to be significantly over-expressed in cancer tissues. These increased proteins included glycolytic enzymes, heat-shock proteins, tumor antigens, cytoskeleton proteins, enzymes involved in detoxification and anti-oxidation systems, and proteins involved in mitochondrial and intracellular signaling pathways. These extensive protein variations indicate that multiple cellular pathways were involved in the process of tumorigenesis, and suggest that multiple protein molecules should be simultaneously targeted as an effective strategy to counter the disease. At least, SCC antigen, G protein, glutathione S-transferase, manganese superoxide dismutase, annexins, voltage-dependent anion channel, cyclophilin A, stratifin and galectin 7 are candidates for targeted proteins. The present findings also demonstrated that rich protein information can be produced by means of proteomic analysis for a better understanding of the oncogenesis and pathogenesis in a global way, which in turn is a basis for the rational designs of diagnostic and therapeutic methods. |
Persistent Identifier | http://hdl.handle.net/10722/48518 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 1.011 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chen, J | en_HK |
dc.contributor.author | He, Q | en_HK |
dc.contributor.author | Yuen, PW | en_HK |
dc.contributor.author | Chiu, J | en_HK |
dc.date.accessioned | 2008-05-22T04:16:02Z | - |
dc.date.available | 2008-05-22T04:16:02Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Proteomics, 2004, v. 4 n. 8, p. 2465-2475 | en_HK |
dc.identifier.issn | 1615-9853 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/48518 | - |
dc.description.abstract | Squamous cell carcinoma (SCC) of the buccal mucosa is an aggressive oral cancer. It mainly occurs in Central and Southeast Asia, and is closely related to the practice of tobacco smoking and betel squid chewing. The high recurrence and low survival rates of buccal SCC require our continued efforts to understand the pathogenesis of the disease for designing better therapeutic strategies. We used proteomic technology to analyze buccal SCC tissues aiming at identifying tumor-associated proteins for the utilization as biomarkers or molecular targets. With the exception of alpha B-crystallin being substantially reduced, a number of proteins were found to be significantly over-expressed in cancer tissues. These increased proteins included glycolytic enzymes, heat-shock proteins, tumor antigens, cytoskeleton proteins, enzymes involved in detoxification and anti-oxidation systems, and proteins involved in mitochondrial and intracellular signaling pathways. These extensive protein variations indicate that multiple cellular pathways were involved in the process of tumorigenesis, and suggest that multiple protein molecules should be simultaneously targeted as an effective strategy to counter the disease. At least, SCC antigen, G protein, glutathione S-transferase, manganese superoxide dismutase, annexins, voltage-dependent anion channel, cyclophilin A, stratifin and galectin 7 are candidates for targeted proteins. The present findings also demonstrated that rich protein information can be produced by means of proteomic analysis for a better understanding of the oncogenesis and pathogenesis in a global way, which in turn is a basis for the rational designs of diagnostic and therapeutic methods. | en_HK |
dc.format.extent | 970320 bytes | - |
dc.format.extent | 254114 bytes | - |
dc.format.mimetype | application/pdf | - |
dc.format.mimetype | application/pdf | - |
dc.language | eng | en_HK |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics | en_HK |
dc.rights | Published in Proteomics, 2004, v. 4 n. 8, p. 2465-2475 | en_HK |
dc.subject | Biomarker | en_HK |
dc.subject | Buccal cancer | en_HK |
dc.subject | Mass spectronomyi fingerprinting | en_HK |
dc.subject | Protein profile | en_HK |
dc.subject | Two-dimensional-polyacrylamide get dectrophoresis | en_HK |
dc.title | Proteomics of buccal squamous cell carcinoma: The involvement of multiple pathways in tumorigenesis | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1615-9853&volume=4&issue=8&spage=2465&epage=2475&date=2004&atitle=Proteomics+of+buccal+squamous+cell+carcinoma:+The+involvement+of+multiple+pathways+in+tumorigenesis | en_HK |
dc.identifier.email | He, Q: qyhe@hkucc.hku.hk | en_HK |
dc.identifier.email | Yuen, PW: pwyuen@hkucc.hku.hk | en_HK |
dc.identifier.email | Chiu, J: jfchiu@hkucc.hku.hk | en_HK |
dc.description.nature | postprint | en_HK |
dc.identifier.doi | 10.1002/pmic.200300762 | en_HK |
dc.identifier.pmid | 15274141 | - |
dc.identifier.scopus | eid_2-s2.0-3543055313 | - |
dc.identifier.hkuros | 91291 | - |
dc.identifier.isi | WOS:000223137300029 | - |
dc.identifier.citeulike | 2625467 | - |
dc.identifier.issnl | 1615-9853 | - |