Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype
Cancer is a disease associated with the deregulation of multiple gene networks. Microarray data has permitted researchers to identify gene panel markers for diagnosis or prognosis of cancer but these are not sufficient to make specific mechanistic assertions about phenotype switches. We propose a st...
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2010-01-01
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doaj-e6f742d3bd084d52998ac637205ad6162020-11-25T03:28:29ZengSAGE PublishingCancer Informatics1176-93512010-01-01910.4137/CIN.S3899Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer PhenotypeJianghui Xiong0Juan Liu1Simon Rayner2Yinghui Li3Shanguang Chen4State Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, P.R. China.School of Computer Science, Wuhan University, Wuhan, P.R. China.Bioinformatics Group, State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, P.R. China.State Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, P.R. China.State Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, P.R. China.Cancer is a disease associated with the deregulation of multiple gene networks. Microarray data has permitted researchers to identify gene panel markers for diagnosis or prognosis of cancer but these are not sufficient to make specific mechanistic assertions about phenotype switches. We propose a strategy to identify putative mechanisms of cancer phenotypes by protein-protein interactions (PPI). We first extracted the logic status of a PPI via the relative expression of the corresponding gene pair. The joint association of a gene pair on a cancer phenotype was calculated by entropy minimization and assessed using a support vector machine. A typical predictor is “ If Src high-expression, and Cav-1 low-expression, then cancer. “ We achieved 90% accuracy on test data with a majority of predictions associated with the MAPK pathway, focal adhesion, apoptosis and cell cycle. Our results can aid in the development of phenotype discrimination biomarkers and identification of putative therapeutic interference targets for drug development.https://doi.org/10.4137/CIN.S3899 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jianghui Xiong Juan Liu Simon Rayner Yinghui Li Shanguang Chen |
spellingShingle |
Jianghui Xiong Juan Liu Simon Rayner Yinghui Li Shanguang Chen Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype Cancer Informatics |
author_facet |
Jianghui Xiong Juan Liu Simon Rayner Yinghui Li Shanguang Chen |
author_sort |
Jianghui Xiong |
title |
Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype |
title_short |
Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype |
title_full |
Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype |
title_fullStr |
Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype |
title_full_unstemmed |
Protein-Protein Interaction Reveals Synergistic Discrimination of Cancer Phenotype |
title_sort |
protein-protein interaction reveals synergistic discrimination of cancer phenotype |
publisher |
SAGE Publishing |
series |
Cancer Informatics |
issn |
1176-9351 |
publishDate |
2010-01-01 |
description |
Cancer is a disease associated with the deregulation of multiple gene networks. Microarray data has permitted researchers to identify gene panel markers for diagnosis or prognosis of cancer but these are not sufficient to make specific mechanistic assertions about phenotype switches. We propose a strategy to identify putative mechanisms of cancer phenotypes by protein-protein interactions (PPI). We first extracted the logic status of a PPI via the relative expression of the corresponding gene pair. The joint association of a gene pair on a cancer phenotype was calculated by entropy minimization and assessed using a support vector machine. A typical predictor is “ If Src high-expression, and Cav-1 low-expression, then cancer. “ We achieved 90% accuracy on test data with a majority of predictions associated with the MAPK pathway, focal adhesion, apoptosis and cell cycle. Our results can aid in the development of phenotype discrimination biomarkers and identification of putative therapeutic interference targets for drug development. |
url |
https://doi.org/10.4137/CIN.S3899 |
work_keys_str_mv |
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