Evidence map›Paper›PMID 27895117›Full record

ArticleThe Journal of biological chemistry2017

Examining Crosstalk among Transforming Growth Factor β, Bone Morphogenetic Protein, and Wnt Pathways.

Adam D Coster, Curtis A Thorne, Lani F Wu, Steven J Altschuler

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. αFrontiers in cell and developmental biology · 2020
    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

4 authors.

Adam D CosterFrom the Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390 and.
Curtis A ThorneFrom the Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390 and.
Lani F WuFrom the Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390 and Lani.Wu@ucsf.edu.
Steven J AltschulerFrom the Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390 and Steven.Altschuler@ucsf.edu.

Funding

Maximizing the predictive power of high-throughput, microscopy-based phenotypic screensR01CA184984 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WU, LANI F · 2014 to 2025
$4.7M
Systems-level role of GSK3 in colonic epithelium homeostasis and drug resistanceR01GM112690 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALTSCHULER, STEVEN J · 2015 to 2018
$1.3M
The role of kinase signaling in intestinal epithelial homeostasisR00DK103126 · NIDDK · UNIVERSITY OF ARIZONA · PI THORNE, CURTIS ANDREW · 2018 to 2020
$747k
The role of kinase signaling in intestinal epithelial homeostasisK99DK103126 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI THORNE, CURTIS ANDREW · 2014 to 2015
$177k
NCI NIH HHS R01 CA184984NIDDK NIH HHS K99 DK103126NIDDK NIH HHS R00 DK103126NIGMS NIH HHS R01 GM112690
6 · The paper itself

Abstract

The integration of morphogenic signals by cells is not well understood. A growing body of literature suggests increasingly complex coupling among classically defined pathways. Given this apparent complexity, it is difficult to predict where, when, or even whether crosstalk occurs. Here, we investigated pairs of morphogenic pathways, previously reported to have multiple points of crosstalk, which either do not share (TGFβ and Wnt/β-catenin) or share (TGFβ and bone morphogenetic protein (BMP)) core signaling components. Crosstalk was measured by the ability of one morphogenic pathway to cross-activate core transcription factors and/or target genes of another morphogenic pathway. In contrast to previous studies, we found a surprising absence of crosstalk between TGFβ and Wnt/β-catenin. Further, we did not observe expected cross-pathway inhibition in between TGFβ and BMP, despite the fact that both use (or could compete) for the shared component SMAD4. Critical to our assays was a separation of timescales, which helped separate crosstalk due to initial signal transduction from subsequent post-transcriptional feedback events. Our study revealed fewer (and different) inter-morphogenic pathway crosstalk connections than expected; even pathways that share components can be insulated from one another.

Indexed as

beta CateninBone Morphogenetic ProteinsCells, CulturedEpithelium, CornealHumansSignal TransductionTransforming Growth Factor betaWnt Proteinsbeta CateninBone Morphogenetic ProteinsTransforming Growth Factor betaWnt Proteinsbone morphogenetic protein (BMP)imagingsignal transductiontranscription factortransforming growth factor β (TGF-β)Wnt signaling

Identifiers

PMID27895117
PMCPMC5217683

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Registered trials

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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.