PathTracer: High-sensitivity detection of differential pathway activity in tumours.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
08 11 2019
Historique:
received: 15 07 2019
accepted: 14 10 2019
entrez: 10 11 2019
pubmed: 11 11 2019
medline: 6 11 2020
Statut: epublish

Résumé

Gene expression profiling of tumours is an important source of information for cancer patient stratification. Detecting subtle alterations of gene expression remains a challenge, however. Here, we propose a novel tool for high-sensitivity detection of differential pathway activity in tumours. For a pathway defined by a collection of genes, the samples are projected onto a low-dimensional manifold in the subspace spanned by those genes. For each sample, a score is next found by calculating the distance between each projected sample and the projection of a subgroup of reference samples. Depending on the aim of the analysis and the available data, the reference samples may represent e.g. normal tissue or tumour samples with a particular genotype or phenotype. The proposed tool, PathTracer, is demonstrated on gene expression data from 1952 invasive breast cancer samples, 10 DCIS, 9 benign samples and 144 tumour adjacent normal breast tissue samples. PathTracer scores are shown to predict survival, clinical subtypes, cellular proliferation and genomic instability. Furthermore, predictions are shown to outperform those obtained with other comparable methods.

Identifiants

pubmed: 31704995
doi: 10.1038/s41598-019-52529-3
pii: 10.1038/s41598-019-52529-3
pmc: PMC6841931
doi:

Substances chimiques

Tumor Suppressor Protein p53 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16332

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Auteurs

Ståle Nygård (S)

Centre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
Bioinformatics core facility, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.

Ole Christian Lingjærde (OC)

Centre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
KG Jebsen Centre for B-cell malignancies, Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Carlos Caldas (C)

Cancer Research UK, Cambridge Research Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.

Eivind Hovig (E)

Centre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.

Anne-Lise Børresen-Dale (AL)

Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.

Åslaug Helland (Å)

Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Department of Oncology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Vilde D Haakensen (VD)

Department of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. vilde.haakensen@gmail.com.
Department of Oncology, Oslo University Hospital, Oslo, Norway. vilde.haakensen@gmail.com.

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Classifications MeSH