Evidence map›Paper›PMID 36077561›Full record

ArticleInternational journal of molecular sciences2022

Immobilization of Wnt Fragment Peptides on Magnetic Nanoparticles or Synthetic Surfaces Regulate Wnt Signaling Kinetics.

Bin Hu, Michael Rotherham, Neil Farrow, Paul Roach, Jon Dobson, Alicia J El Haj

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.7field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  5. 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

6 authors at 5 institutions in 3 countries.

Bin HuSchool of Pharmacy and Bioengineering, Guy Hilton Research Center, Keele University, Thornburrow Drive, Hartshill, Stoke-on-Trent, Staffordshire ST4 7QB, UK.ORCID 0000-0002-5642-8300
Michael RotherhamHealthcare Technologies Institute, School of Chemical Engineering, University of Birmingham, Heritage Building, Mindelsohn Way, Birmingham B15 2TH, UK.ORCID 0000-0002-9297-7681
Neil FarrowSchool of Pharmacy and Bioengineering, Guy Hilton Research Center, Keele University, Thornburrow Drive, Hartshill, Stoke-on-Trent, Staffordshire ST4 7QB, UK.
Paul RoachSchool of Pharmacy and Bioengineering, Guy Hilton Research Center, Keele University, Thornburrow Drive, Hartshill, Stoke-on-Trent, Staffordshire ST4 7QB, UK.ORCID 0000-0003-4135-9733
Jon DobsonJ Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL 32611, USA.
Alicia J El HajSchool of Pharmacy and Bioengineering, Guy Hilton Research Center, Keele University, Thornburrow Drive, Hartshill, Stoke-on-Trent, Staffordshire ST4 7QB, UK.
Keele University · GBLoughborough University · GBNational Center for Nanoscience and Technology · CNUniversity of Birmingham · GBUniversity of Florida · US

Funding

Engineering and Physical Sciences Research Council EP/I032002/1European Research Council 789119Medical Research Council MR/K026666/1Medical Research Council MR/R015635/1MRC UK Regenerative Medicine Platform Hubs MR/K026666/1, MR/R015635/1
6 · The paper itself

Abstract

Wnt signaling plays an important role in embryogenesis and adult stem cell homeostasis. Its diminished activation is implicated in osteoporosis and degenerative neural diseases. However, systematic administration of Wnt-signaling agonists carries risk, as aberrantly activated Wnt/β-catenin signaling is linked to cancer. Therefore, technologies for local modulation and control of Wnt signaling targeted to specific sites of disease or degeneration have potential therapeutic value in the treatment of degenerative diseases. We reported a facile approach to locally activate the canonical Wnt signaling cascade using nanomagnetic actuation or ligand immobilized platforms. Using a human embryonic kidney (HEK293) Luc-TCF/LEF reporter cell line, we demonstrated that targeting the cell membrane Wnt receptor, Frizzled 2, with peptide-tagged magnetic nanoparticles (MNPs) triggered canonical Wnt signaling transduction when exposed to a high-gradient, time-varying magnetic field, and the induced TCF/LEF signal transduction was shown to be avidity-dependent. We also demonstrated that the peptide retained signaling activity after functionalization onto glass surfaces, providing a versatile platform for drug discovery or recreation of the cell niche. In conclusion, these results showed that peptide-mediated Wnt signaling kinetics depended not only on ligand concentration but also on the presentation method of the ligand, which may be further modulated by magnetic actuation. This has important implications when designing future therapeutic platforms involving Wnt mimetics.

Indexed as

Magnetite NanoparticlesWnt Signaling Pathwaybeta CateninHEK293 CellsHumansLigandsPeptidesWnt Proteinsbeta CateninLigandsMagnetite NanoparticlesPeptidesWnt Proteinsmagnetic force bioreactormagnetic nanoparticlemechanotransductionnanomagnetic actuationpeptide immobilizationtissue engineeringWnt/β-catenin

Identifiers

PMID36077561
PMCPMC9456016
OpenAlexW4294733324

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.