Evidence map›Paper›PMID 23912898›Full record

ReviewCellular and molecular life sciences : CMLS2014

Recruitment and retention: factors that affect pericyte migration.

Kristina Y Aguilera, Rolf A Brekken

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Eppur si muove: the dynamic brain pericyte.Fluids and barriers of the CNS · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Current neuropharmacology · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. CD146International journal of molecular sciences · 2022
    Article
  19. Efficiency ofExperimental and therapeutic medicine · 2021
    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

2 authors at 2 institutions in 1 country.

Kristina Y AguileraDivision of Surgical Oncology, Department of Surgery, Hamon Center for Therapeutic Oncology Research, University of Texas Southwestern Medical Center, 6000 Harry Hines Blvd, Dallas, TX, 75390-8593, USA.
Rolf A Brekken
Southwestern Medical Center · USThe University of Texas Southwestern Medical Center · US

Funding

Matricellular proteins as regulators of tumor progressionR01CA118240 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BREKKEN, ROLF A · 2007 to 2010
$1.2M
SPARC AS A REGULATOR OF VEGF ACTIVITYF32HL010352 · NHLBI · THE HOPE HEART INSTITUTE · PI BREKKEN, ROLF A · 2000 to 2002
$82k
SPARC as a regulator of collagen signaling in Pancreatic CancerF31CA168350 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI AGUILERA, KRISTINA YOLANDA · 2012 to 2015
$80k
NCI NIH HHS CA168350NCI NIH HHS F31 CA168350NCI NIH HHS R01 CA118240NCI NIH HHS R01CA118240NHLBI NIH HHS F32 HL010352
6 · The paper itself

Abstract

Pericytes are critical for vascular morphogenesis and contribute to several pathologies, including cancer development and progression. The mechanisms governing pericyte migration and differentiation are complex and have not been fully established. Current literature suggests that platelet-derived growth factor/platelet-derived growth factor receptor-β, sphingosine 1-phosphate/endothelial differentiation gene-1, angiopoietin-1/tyrosine kinase with immunoglobulin-like and EGF-like domains 2, angiopoietin-2/tyrosine kinase with immunoglobulin-like and EGF-like domains 2, transforming growth factor β/activin receptor-like kinase 1, transforming growth factor β/activin receptor-like kinase 5, Semaphorin-3A/Neuropilin, and matrix metalloproteinase activity regulate the recruitment of pericytes to nascent vessels. Interestingly, many of these pathways are directly affected by secreted protein acidic and rich in cysteine (SPARC). Here, we summarize the function of these factors in pericyte migration and discuss if and how SPARC might influence these activities and thus provide an additional layer of control for the recruitment of vascular support cells. Additionally, the consequences of targeted inhibition of pericytes in tumors and the current understanding of pericyte recruitment in pathological environments are discussed.

Indexed as

Cell MovementHumansIntercellular Signaling Peptides and ProteinsMetalloendopeptidasesMyocytes, Smooth MuscleNeovascularization, PhysiologicOsteonectinPericytesProtein KinasesSignal TransductionVesicular Transport ProteinsIntercellular Signaling Peptides and ProteinsMetalloendopeptidasesOsteonectinProtein KinasesSPARC protein, humanVesicular Transport Proteins

Identifiers

PMID23912898
PMCPMC3880607
OpenAlexW2066088219

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.