Evidence map›Paper›PMID 26808411›Full record

ArticleExperimental cell research2016

MAGP2 controls Notch via interactions with RGD binding integrins: Identification of a novel ECM-integrin-Notch signaling axis.

Peter Deford, Kasey Brown, Rae Lee Richards, Aric King, Kristin Newburn, Katherine Westover, Allan R Albig

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. International journal of molecular sciences · 2025
    Article
  4. Loss of MFAP5 and Its Effect on Skin Homeostasis and Wound Healing.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Integrins control epithelial stem cell proliferation in theFrontiers in cell and developmental biology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Stromal fibroblast-derived MFAP5 promotes the invasion and migration of breast cancer cells via Notch1/slug signaling.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Article
  18. Loss of microfibril-associated protein 5 (MFAP5) expression in colon cancer stroma.Virchows Archiv : an international journal of pathology · 2020
    Article
  19. Article
  20. Review
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 1 country.

Peter DefordDepartment of Biology, Boise State University, Boise, ID 83725, United States.
Kasey BrownDepartment of Biology, Indiana State University, Terre Haute, IN 47809, United States.
Rae Lee RichardsDepartment of Biology, Indiana State University, Terre Haute, IN 47809, United States.
Aric KingDepartment of Biology, Indiana State University, Terre Haute, IN 47809, United States.
Kristin NewburnDepartment of Biology, Indiana State University, Terre Haute, IN 47809, United States.
Katherine WestoverDepartment of Biology, Boise State University, Boise, ID 83725, United States.
Allan R AlbigBiomolecular Sciences PhD Program, Boise State University, Boise, ID 83725, United States; Department of Biology, Boise State University, Boise, ID 83725, United States. Electronic address: AllanAlbig@boisestate.edu.
Indiana State University · USBoise State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
UNDERGRADUATE COLLEGE OUTREACH PROGRAMP20RR016454 · NCRR · UNIVERSITY OF IDAHO · PI CHASE, JENNIFER R · 2001 to 2011
$35.3M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2014 to 2023
$22.7M
CELLULAR AND MOLECULAR BIOLOGYT32GM007231 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VAN DOREN, MARK B · 1985 to 2020
$18.4M
Identification and Characterization of an Integrin - Notch Signaling AxisR15GM102852 · NIGMS · BOISE STATE UNIVERSITY · PI ALBIG, ALLAN R · 2012 to 2017
$716k
Mechanisms by which MAGP-2 Promotes AngiogenesisR15CA133829 · NCI · INDIANA STATE UNIVERSITY · PI ALBIG, ALLAN R · 2009 to 2010
$284k
NCI NIH HHS 1R15CA133829-01NCI NIH HHS R15 CA133829NCRR NIH HHS P20 RR016454NCRR NIH HHS P20RR016454NIGMS NIH HHS 1R15GM102852-01NIGMS NIH HHS P20 GM103408NIGMS NIH HHS P20GM103408NIGMS NIH HHS P20 GM109095NIGMS NIH HHS R15 GM102852NIGMS NIH HHS T32 GM007231
6 · The paper itself

Abstract

Canonical Notch signaling involves Notch receptor activation via interaction with cell surface bound Notch ligand. Recent findings also indicate that Notch signaling may be modulated by cross-talk with other signaling mechanisms. The ECM protein MAGP2 was previously shown to regulate Notch in a cell type dependent manner, although the molecular details of this interaction have not been dissected. Here, we report that MAGP2 cell type specific control of Notch is independent of individual Notch receptor-ligand combinations but dependent on interaction with RGD binding integrins. Overexpressed MAGP2 was found to suppress transcriptional activity from the Notch responsive Hes1 promoter activity in endothelial cells, while overexpression of a RGD→RGE MAGP2 mutant increased Notch signaling in the same cell type. This effect was not unique to MAGP2 since the RGD domain of the ECM protein EGFL7 was also found to be an important modulator of Hes1 promoter activity. Independently of MAGP2 or EGFL7, inhibition of RGD-binding integrins with soluble RGD peptides also increased accumulation of active N1ICD fragments and Notch responsive promoter activity independently of changes in Notch1, Jag1, or Dll4 expression. Finally, β1 or β3 integrin blocking antibodies also enhanced Notch signaling. Collectively, these results answer the question of how MAGP2 controls cell type dependent Notch signaling, but more importantly uncover a new mechanism to understand how extracellular matrices and cellular environments impact Notch signaling.

Indexed as

Signal TransductionContractile ProteinsGlycoproteinsHumansIntegrinsIntercellular Signaling Peptides and ProteinsOligopeptidesReceptors, Notcharginyl-glycyl-aspartic acidContractile ProteinsGlycoproteinsIntegrinsIntercellular Signaling Peptides and ProteinsMFAP5 protein, humanOligopeptidesReceptors, NotchCell signalingExtracellular matrixIntegrinNotch

Identifiers

PMID26808411
PMCPMC4817345
OpenAlexW2275732895

What OpenQuestion holds

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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.