Evidence map›Paper›PMID 18621714›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

FOXC2 controls Ang-2 expression and modulates angiogenesis, vascular patterning, remodeling, and functions in adipose tissue.

Yuan Xue, Renhai Cao, Daniel Nilsson, Shaohua Chen, Rickard Westergren, Eva-Maria Hedlund, Cecile Martijn, Lena Rondahl, Per Krauli, Erik Walum and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 110 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Role of the Fox Gene in Breast Cancer Progression.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. KRAS mutation-driven angiopoietin 2 bestows anti-VEGF resistance in epithelial carcinomas.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Generation of Vascular Networks from AdipocytesInternational journal of cell science & molecular biology · 2019
    Article
  18. Review
  19. Transcription and microRNA Profiling of Cultured Human Tympanic Membrane Epidermal Keratinocytes.Journal of the Association for Research in Otolaryngology : JARO · 2018
    Article
  20. 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

12 authors at 4 institutions in 2 countries.

Yuan XueDepartment of Microbiology, Laboratory of Angiogenesis Research, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden.
Renhai Cao
Daniel Nilsson
Shaohua Chen
Rickard Westergren
Eva-Maria Hedlund
Cecile Martijn
Lena Rondahl
Per Krauli
Erik Walum
Sven Enerbäck
Yihai Cao
Karolinska Institutet · SESwedish Orphan Biovitrum (Sweden) · SEUniversity of Gothenburg · SEUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipogenesis is spatiotemporally coupled to angiogenesis throughout adult life, and the interplay between these two processes is communicated by multiple factors. Here we show that in a transgenic mouse model, increased expression of forkhead box C2 (FOXC2) in the adipose tissue affects angiogenesis, vascular patterning, and functions. White and brown adipose tissues contain a considerably high density of microvessels appearing as vascular plexuses, which show redistribution of vascular smooth muscle cells and pericytes. Dysfunction of these primitive vessels is reflected by impairment of skin wound healing. We further provide a mechanistic insight of the vascular phenotype by showing that FOXC2 controls Ang-2 expression by direct activation of its promoter in adipocytes. Remarkably, an Ang-2-specific antagonist almost completely reverses this vascular phenotype. Thus, the FOXC2-Ang-2 signaling system is crucial for controlling adipose vascular function, which is part of an adaptation to increased adipose tissue metabolism.

Indexed as

AdipocytesAdipogenesisAdipose TissueAdipose Tissue, BrownAngiopoietin-2AnimalsForkhead Transcription FactorsGene Expression RegulationMiceMice, TransgenicNeovascularization, PhysiologicPhenotypePromoter Regions, GeneticSignal TransductionAngiopoietin-2Forkhead Transcription Factorsmesenchyme fork head 1 protein

Identifiers

PMID18621714
PMCPMC2481379
OpenAlexW1966561876

What OpenQuestion holds

Textmetadata
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.