Evidence map›Paper›PMID 31704995›Full record

ArticleScientific reports2019

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

Ståle Nygård, Ole Christian Lingjærde, Carlos Caldas, Eivind Hovig, Anne-Lise Børresen-Dale, Åslaug Helland, Vilde D Haakensen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Ståle NygårdCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
Ole Christian LingjærdeCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
Carlos CaldasCancer Research UK, Cambridge Research Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-3547-1489
Eivind HovigCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.ORCID http://orcid.org/0000-0002-9103-1077
Anne-Lise Børresen-DaleDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Åslaug HellandDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Vilde D HaakensenDepartment of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. vilde.haakensen@gmail.com.ORCID http://orcid.org/0000-0003-0864-3628
Oslo University Hospital · NOUniversity of Cambridge · GB

Funding

Cancer Research UK 16942
6 · The paper itself

Abstract

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.

Indexed as

Gene Expression ProfilingBreast NeoplasmsComputational BiologyMutationOligonucleotide Array Sequence AnalysisTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID31704995
PMCPMC6841931
OpenAlexW2987853607

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.