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Prediction of a gene regulatory network linked to prostate cancer from gene expression, microRNA and clinical data

Eric Bonnet UGent, Tom Michoel UGent and Yves Van de Peer UGent (2010) BIOINFORMATICS. 26(18). p.i638-i644
abstract
Motivation: Cancer is a complex disease, triggered by mutations in multiple genes and pathways. There is a growing interest in the application of systems biology approaches to analyze various types of cancer-related data to understand the overwhelming complexity of changes induced by the disease. Results: We reconstructed a regulatory module network using gene expression, microRNA expression and a clinical parameter, all measured in lymphoblastoid cell lines derived from patients having aggressive or non-aggressive forms of prostate cancer. Our analysis identified several modules enriched in cell cycle-related genes as well as novel functional categories that might be linked to prostate cancer. Almost one-third of the regulators predicted to control the expression levels of the modules are microRNAs. Several of them have already been characterized as causal in various diseases, including cancer. We also predicted novel microRNAs that have never been associated to this type of tumor. Furthermore, the condition-dependent expression of several modules could be linked to the value of a clinical parameter characterizing the aggressiveness of the prostate cancer. Taken together, our results help to shed light on the consequences of aggressive and non-aggressive forms of prostate cancer.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (proceedingsPaper)
publication status
published
subject
keyword
PROLIFERATION, CELL-LINES, SYSTEMS BIOLOGY, MODULE NETWORKS, PROGRESSION, MORTALITY, DISEASE, FOXM1, P53
journal title
BIOINFORMATICS
Bioinformatics
volume
26
issue
18
pages
i638 - i644
conference name
9th European Conference on Computational Biology
conference location
Ghent, Belgium
conference start
2010-09-26
conference end
2010-09-29
Web of Science type
Proceedings Paper
Web of Science id
000281714100034
JCR category
MATHEMATICAL & COMPUTATIONAL BIOLOGY
JCR impact factor
4.877 (2010)
JCR rank
2/35 (2010)
JCR quartile
1 (2010)
ISSN
1367-4803
DOI
10.1093/bioinformatics/btq395
language
English
UGent publication?
yes
classification
A1
copyright statement
I have retained and own the full copyright for this publication
id
1061935
handle
http://hdl.handle.net/1854/LU-1061935
date created
2010-10-21 14:31:29
date last changed
2012-09-19 14:03:40
@article{1061935,
  abstract     = {Motivation: Cancer is a complex disease, triggered by mutations in multiple genes and pathways. There is a growing interest in the application of systems biology approaches to analyze various types of cancer-related data to understand the overwhelming complexity of changes induced by the disease.
Results: We reconstructed a regulatory module network using gene expression, microRNA expression and a clinical parameter, all measured in lymphoblastoid cell lines derived from patients having aggressive or non-aggressive forms of prostate cancer. Our analysis identified several modules enriched in cell cycle-related genes as well as novel functional categories that might be linked to prostate cancer. Almost one-third of the regulators predicted to control the expression levels of the modules are microRNAs. Several of them have already been characterized as causal in various diseases, including cancer. We also predicted novel microRNAs that have never been associated to this type of tumor. Furthermore, the condition-dependent expression of several modules could be linked to the value of a clinical parameter characterizing the aggressiveness of the prostate cancer. Taken together, our results help to shed light on the consequences of aggressive and non-aggressive forms of prostate cancer.},
  author       = {Bonnet, Eric and Michoel, Tom and Van de Peer, Yves},
  issn         = {1367-4803},
  journal      = {BIOINFORMATICS},
  keyword      = {PROLIFERATION,CELL-LINES,SYSTEMS BIOLOGY,MODULE NETWORKS,PROGRESSION,MORTALITY,DISEASE,FOXM1,P53},
  language     = {eng},
  location     = {Ghent, Belgium},
  number       = {18},
  pages        = {i638--i644},
  title        = {Prediction of a gene regulatory network linked to prostate cancer from gene expression, microRNA and clinical data},
  url          = {http://dx.doi.org/10.1093/bioinformatics/btq395},
  volume       = {26},
  year         = {2010},
}

Chicago
Bonnet, Eric, Tom Michoel, and Yves Van de Peer. 2010. “Prediction of a Gene Regulatory Network Linked to Prostate Cancer from Gene Expression, microRNA and Clinical Data.” Bioinformatics 26 (18): i638–i644.
APA
Bonnet, E., Michoel, T., & Van de Peer, Y. (2010). Prediction of a gene regulatory network linked to prostate cancer from gene expression, microRNA and clinical data. BIOINFORMATICS, 26(18), i638–i644. Presented at the 9th European Conference on Computational Biology.
Vancouver
1.
Bonnet E, Michoel T, Van de Peer Y. Prediction of a gene regulatory network linked to prostate cancer from gene expression, microRNA and clinical data. BIOINFORMATICS. 2010;26(18):i638–i644.
MLA
Bonnet, Eric, Tom Michoel, and Yves Van de Peer. “Prediction of a Gene Regulatory Network Linked to Prostate Cancer from Gene Expression, microRNA and Clinical Data.” BIOINFORMATICS 26.18 (2010): i638–i644. Print.