Evidence map›Paper›PMID 36967195›Full record

ArticleCurrent topics in developmental biology2023

Non-canonical WNT5A-ROR signaling: New perspectives on an ancient developmental pathway.

Sara E Konopelski Snavely, Srisathya Srinivasan, Courtney A Dreyer, Jia Tan, Kermit L Carraway, Hsin-Yi Henry Ho

Open access · greenAbstract read
In one paragraph

Article in Current topics in developmental biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
12.5field-weighted citation impact, top 1% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Sara E Konopelski SnavelyDepartment of Cell Biology and Human Anatomy, University of California Davis, School of Medicine, Davis, CA, United States.
Srisathya SrinivasanDepartment of Cell Biology and Human Anatomy, University of California Davis, School of Medicine, Davis, CA, United States.
Courtney A DreyerDepartment of Biochemistry and Molecular Medicine, UC Davis Comprehensive Cancer Center, University of California Davis, School of Medicine, Sacramento, CA, United States.
Jia TanDepartment of Cell Biology and Human Anatomy, University of California Davis, School of Medicine, Davis, CA, United States.
Kermit L CarrawayDepartment of Biochemistry and Molecular Medicine, UC Davis Comprehensive Cancer Center, University of California Davis, School of Medicine, Sacramento, CA, United States.
Hsin-Yi Henry HoDepartment of Cell Biology and Human Anatomy, University of California Davis, School of Medicine, Davis, CA, United States. Electronic address: hyhho@ucdavis.edu.
University of California, Davis · US

Funding

Function and regulatory mechanisms of the Wnt5a-Ror morphogenetic pathwayR35GM144341 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Hsin-Yi Henry Ho · 2022 to 2026
$2.2M
Lysosomal-mitochondrial signaling in non-apoptotic cancer cell deathR01CA250211 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARRAWAY, KERMIT L · 2020 to 2024
$2.2M
Deciphering Wnt-Ror signaling in cytoskeletal regulation and tissue shape controlR35GM119574 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HO, HSIN-YI HENRY · 2016 to 2021
$2.0M
Planar cell polarity pathway contribution to breast cancer metastasisR01CA230742 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARRAWAY, KERMIT L · 2019 to 2023
$2.0M
NCI NIH HHS R01 CA230742NCI NIH HHS R01 CA250211NIGMS NIH HHS R35 GM119574NIGMS NIH HHS R35 GM144341
6 · The paper itself

Abstract

Deciphering non-canonical WNT signaling has proven to be both fascinating and challenging. Discovered almost 30 years ago, non-canonical WNT ligands signal independently of the transcriptional co-activator β-catenin to regulate a wide range of morphogenetic processes during development. The molecular and cellular mechanisms that underlie non-canonical WNT function, however, remain nebulous. Recent results from various model systems have converged to define a core non-canonical WNT pathway consisting of the prototypic non-canonical WNT ligand, WNT5A, the receptor tyrosine kinase ROR, the seven transmembrane receptor Frizzled and the cytoplasmic scaffold protein Dishevelled. Importantly, mutations in each of these signaling components cause Robinow syndrome, a congenital disorder characterized by profound tissue morphogenetic abnormalities. Moreover, dysregulation of the pathway has also been linked to cancer metastasis. As new knowledge concerning the WNT5A-ROR pathway continues to grow, modeling these mutations will likely provide crucial insights into both the physiological regulation of the pathway and the etiology of WNT5A-ROR-driven diseases.

Indexed as

Receptor Tyrosine Kinase-like Orphan ReceptorsWnt ProteinsMorphogenesisSignal TransductionWnt-5a ProteinWnt Signaling PathwayReceptor Tyrosine Kinase-like Orphan ReceptorsWnt-5a ProteinWnt ProteinsCancer metastasisDishevelledDVLFrizzledFZDNon-canonical WNT signalingOmodysplasiaRobinow syndromeRORTissue morphogenesisWNT5A

Identifiers

PMID36967195
PMCPMC11042798
OpenAlexW4327794844

What Socratic holds

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LicenceTDM
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 Socratic graph.