Evidence map›Paper›PMID 28725467›Full record

ArticleNPJ systems biology and applications2016

Pathways on demand: automated reconstruction of human signaling networks.

Anna Ritz, Christopher L Poirel, Allison N Tegge, Nicholas Sharp, Kelsey Simmons, Allison Powell, Shiv D Kale, T M Murali

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in NPJ systems biology and applications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 69 citations in OpenAlex.

  1. A Framework for Benchmarking Pathway Reconstruction Algorithms.bioRxiv : the preprint server for biology · 2026
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  3. Logic-based machine learning predicts how escitalopram attenuates cardiomyocyte hypertrophy.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  10. Computational Construction of Toxicant Signaling Networks.Chemical research in toxicology · 2023
    Article
  11. Graph algorithms for predicting subcellular localization at the pathway levelPacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Anna RitzDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Christopher L PoirelDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Allison N TeggeDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Nicholas SharpDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Kelsey SimmonsBiocomplexity Institute, Virginia Tech, Blacksburg, VA, USA.
Allison PowellBiocomplexity Institute, Virginia Tech, Blacksburg, VA, USA.
Shiv D KaleBiocomplexity Institute, Virginia Tech, Blacksburg, VA, USA.
T M MuraliDepartment of Computer Science, Virginia Tech, Blacksburg, VA, USA.
Virginia Tech · US

Funding

Integrating Top-Down and Bottom-Up Models in Systems Biology with Application toR01GM095955 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI MURALI, T M · 2011 to 2015
$2.0M
Computing hepatic intercellular communications in response to toxicant exposuresF32ES024062 · NIEHS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI TEGGE, ALLISON N · 2014 to 2016
$130k
NIEHS NIH HHS F32 ES024062NIGMS NIH HHS R01 GM095955
6 · The paper itself

Abstract

Signaling pathways are a cornerstone of systems biology. Several databases store high-quality representations of these pathways that are amenable for automated analyses. Despite painstaking and manual curation, these databases remain incomplete. We present PATHLINKER, a new computational method to reconstruct the interactions in a signaling pathway of interest. PATHLINKER efficiently computes multiple short paths from the receptors to transcriptional regulators (TRs) in a pathway within a background protein interaction network. We use PATHLINKER to accurately reconstruct a comprehensive set of signaling pathways from the NetPath and KEGG databases. We show that PATHLINKER has higher precision and recall than several state-of-the-art algorithms, while also ensuring that the resulting network connects receptor proteins to TRs. PATHLINKER's reconstruction of the Wnt pathway identified CFTR, an ABC class chloride ion channel transporter, as a novel intermediary that facilitates the signaling of Ryk to Dab2, which are known components of Wnt/β-catenin signaling. In HEK293 cells, we show that the Ryk-CFTR-Dab2 path is a novel amplifier of β-catenin signaling specifically in response to Wnt 1, 2, 3, and 3a of the 11 Wnts tested. PATHLINKER captures the structure of signaling pathways as represented in pathway databases better than existing methods. PATHLINKER's success in reconstructing pathways from NetPath and KEGG databases point to its applicability for complementing manual curation of these databases. PATHLINKER may serve as a promising approach for prioritizing proteins and interactions for experimental study, as illustrated by its discovery of a novel pathway in Wnt/β-catenin signaling. Our supplementary website at http://bioinformatics.cs.vt.edu/~murali/supplements/2016-sys-bio-applications-pathlinker/ provides links to the PATHLINKER software, input datasets, PATHLINKER reconstructions of NetPath pathways, and links to interactive visualizations of these reconstructions on GraphSpace.

Identifiers

PMID28725467
PMCPMC5516854
OpenAlexW2317662115

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.