On the reproducibility of results of pathway analysis in genome-wide expression studies of colorectal cancers (Articolo in rivista)

Type
Label
  • On the reproducibility of results of pathway analysis in genome-wide expression studies of colorectal cancers (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Alternative label
  • R. Maglietta(a), A. Distaso(a), A. Piepoli(b), O. Palumbo(c), M. Carella(c), A. D’Addabbo(a), S. Mukherjee(d), N. Ancona(a) (2010)
    On the reproducibility of results of pathway analysis in genome-wide expression studies of colorectal cancers
    in Journal of biomedical informatics
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • R. Maglietta(a), A. Distaso(a), A. Piepoli(b), O. Palumbo(c), M. Carella(c), A. D’Addabbo(a), S. Mukherjee(d), N. Ancona(a) (literal)
Pagina inizio
  • 397 (literal)
Pagina fine
  • 397-40 (literal)
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  • Q2 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 43 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • a Istituto di Studi sui Sistemi Intelligenti per l'Automazione, CNR, Via Amendola 122/D-I, Bari, Italy b Unità Operativa di Gastroenterologia, IRCCS, ''Casa Sollievo della Sofferenza\"-Ospedale, 71013 San Giovanni Rotondo (FG), Italy c Servizio di Genetica Medica, IRCCS, ''Casa Sollievo della Sofferenza\"-Ospedale, 71013 San Giovanni Rotondo (FG), Italy d Institute for Genome Science and Policy, Duke University, Durham, NC, USA (literal)
Titolo
  • On the reproducibility of results of pathway analysis in genome-wide expression studies of colorectal cancers (literal)
Abstract
  • One of the major problems in genomics and medicine is the identification of gene networks and pathways deregulated in complex and polygenic diseases, like cancer. In this paper, we address the problem of assessing the variability of results of pathways analysis identified in different and independent genome wide expression studies, in which the same phenotypic conditions are assayed. To this end, we assessed the deregulation of 1891 curated gene sets in four independent gene expression data sets of subjects affected by colorectal cancer (CRC). In this comparison we used two well-founded statistical models for evaluating deregulation of gene networks. We found that the results of pathway analysis in expression studies are highly reproducible. Our study revealed 53 pathways identified by the two methods in all the four data sets analyzed with high statistical significance and strong biological relevance with the pathology examined. This set of pathways associated to single markers as well as to whole biological processes altered constitutes a signature of the disease which sheds light on the genetics bases of CRC. (literal)
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