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Article: Artificial neural networks and decision tree model analysis of liver cancer proteomes
Title | Artificial neural networks and decision tree model analysis of liver cancer proteomes |
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Authors | |
Keywords | ANN Cancer proteome CART Classification Hepatocellular carcinoma |
Issue Date | 2007 |
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description |
Citation | Biochemical And Biophysical Research Communications, 2007, v. 361 n. 1, p. 68-73 How to Cite? |
Abstract | Hepatocellular carcinoma (HCC) is a heterogeneous cancer and usually diagnosed at late advanced tumor stages of high lethality. The present study attempted to obtain a proteome-wide analysis of HCC in comparison with adjacent non-tumor liver tissues, in order to facilitate biomarkers' discovery and to investigate the mechanisms of HCC development. A cohort of 66 Chinese patients with HCC was included for proteomic profiling study by two-dimensional gel electrophoresis (2-DE) analysis. Artificial neural network (ANN) and decision tree (CART) data-mining methods were employed to analyze the profiling data and to delineate significant patterns and trends for discriminating HCC from non-malignant liver tissues. Protein markers were identified by tandem MS/MS. A total of 132 proteome datasets were generated by 2-DE expression profiling analysis, and each with 230 consolidated protein expression intensities. Both the data-mining algorithms successfully distinguished the HCC phenotype from other non-malignant liver samples. The detection sensitivity and specificity of ANN were 96.97% and 87.88%, while those of CART were 81.82% and 78.79%, respectively. The three biological classifiers in the CART model were identified as cytochrome b5, heat shock 70 kDa protein 8 isoform 2, and cathepsin B. The 2-DE-based proteomic profiling approach combined with the ANN or CART algorithm yielded satisfactory performance on identifying HCC and revealed potential candidate cancer biomarkers. © 2007 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/81617 |
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.770 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Luk, JM | en_HK |
dc.contributor.author | Lam, BY | en_HK |
dc.contributor.author | Lee, NPY | en_HK |
dc.contributor.author | Ho, DW | en_HK |
dc.contributor.author | Sham, PC | en_HK |
dc.contributor.author | Chen, L | en_HK |
dc.contributor.author | Peng, J | en_HK |
dc.contributor.author | Leng, X | en_HK |
dc.contributor.author | Day, PJ | en_HK |
dc.contributor.author | Fan, ST | en_HK |
dc.date.accessioned | 2010-09-06T08:19:56Z | - |
dc.date.available | 2010-09-06T08:19:56Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Biochemical And Biophysical Research Communications, 2007, v. 361 n. 1, p. 68-73 | en_HK |
dc.identifier.issn | 0006-291X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/81617 | - |
dc.description.abstract | Hepatocellular carcinoma (HCC) is a heterogeneous cancer and usually diagnosed at late advanced tumor stages of high lethality. The present study attempted to obtain a proteome-wide analysis of HCC in comparison with adjacent non-tumor liver tissues, in order to facilitate biomarkers' discovery and to investigate the mechanisms of HCC development. A cohort of 66 Chinese patients with HCC was included for proteomic profiling study by two-dimensional gel electrophoresis (2-DE) analysis. Artificial neural network (ANN) and decision tree (CART) data-mining methods were employed to analyze the profiling data and to delineate significant patterns and trends for discriminating HCC from non-malignant liver tissues. Protein markers were identified by tandem MS/MS. A total of 132 proteome datasets were generated by 2-DE expression profiling analysis, and each with 230 consolidated protein expression intensities. Both the data-mining algorithms successfully distinguished the HCC phenotype from other non-malignant liver samples. The detection sensitivity and specificity of ANN were 96.97% and 87.88%, while those of CART were 81.82% and 78.79%, respectively. The three biological classifiers in the CART model were identified as cytochrome b5, heat shock 70 kDa protein 8 isoform 2, and cathepsin B. The 2-DE-based proteomic profiling approach combined with the ANN or CART algorithm yielded satisfactory performance on identifying HCC and revealed potential candidate cancer biomarkers. © 2007 Elsevier Inc. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/wps/find/journaldescription.cws_home/622790/description | en_HK |
dc.relation.ispartof | Biochemical and Biophysical Research Communications | en_HK |
dc.subject | ANN | en_HK |
dc.subject | Cancer proteome | en_HK |
dc.subject | CART | en_HK |
dc.subject | Classification | en_HK |
dc.subject | Hepatocellular carcinoma | en_HK |
dc.title | Artificial neural networks and decision tree model analysis of liver cancer proteomes | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0006-291X&volume=361&issue=1&spage=68&epage=73&date=2007&atitle=Artificial+neural+networks+and+decision+tree+model+analysis+of+liver+cancer+proteomes | en_HK |
dc.identifier.email | Luk, JM: jmluk@hkucc.hku.hk | en_HK |
dc.identifier.email | Lee, NPY: nikkilee@hku.hk | en_HK |
dc.identifier.email | Sham, PC: pcsham@hku.hk | en_HK |
dc.identifier.email | Fan, ST: stfan@hku.hk | en_HK |
dc.identifier.authority | Luk, JM=rp00349 | en_HK |
dc.identifier.authority | Lee, NPY=rp00263 | en_HK |
dc.identifier.authority | Sham, PC=rp00459 | en_HK |
dc.identifier.authority | Fan, ST=rp00355 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.bbrc.2007.06.172 | en_HK |
dc.identifier.pmid | 17644064 | - |
dc.identifier.scopus | eid_2-s2.0-34548693705 | en_HK |
dc.identifier.hkuros | 133126 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34548693705&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 361 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 68 | en_HK |
dc.identifier.epage | 73 | en_HK |
dc.identifier.isi | WOS:000248659000012 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Luk, JM=7006777791 | en_HK |
dc.identifier.scopusauthorid | Lam, BY=7102023588 | en_HK |
dc.identifier.scopusauthorid | Lee, NPY=7402722690 | en_HK |
dc.identifier.scopusauthorid | Ho, DW=7402971906 | en_HK |
dc.identifier.scopusauthorid | Sham, PC=34573429300 | en_HK |
dc.identifier.scopusauthorid | Chen, L=7409441990 | en_HK |
dc.identifier.scopusauthorid | Peng, J=7401958598 | en_HK |
dc.identifier.scopusauthorid | Leng, X=7102492468 | en_HK |
dc.identifier.scopusauthorid | Day, PJ=7202148832 | en_HK |
dc.identifier.scopusauthorid | Fan, ST=7402678224 | en_HK |
dc.identifier.citeulike | 2933448 | - |
dc.identifier.issnl | 0006-291X | - |