Evidence map›Paper›PMID 25019063›Full record

ArticleFrontiers in oncology2014

Nestin(+) tissue-resident multipotent stem cells contribute to tumor progression by differentiating into pericytes and smooth muscle cells resulting in blood vessel remodeling.

Diana Klein, Nicole Meissner, Veronika Kleff, Holger Jastrow, Masahiro Yamaguchi, Süleyman Ergün, Verena Jendrossek

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.3field-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

35 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Circulating Nestin-GFPStem cell reviews and reports · 2021
    Article
  9. Review
  10. Article
  11. Do not keep it simple: recent advances in the generation of complex organoids.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  12. Review
  13. Review
  14. Review
  15. Amniotic epithelial cells reverse abnormal vascular structure and function in endometrial carcinoma.International journal of clinical and experimental pathology · 2019
    Article
  16. Article
  17. Review
  18. 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 2 countries.

Diana KleinInstitute for Cell Biology (Cancer Research), University Hospital Essen, University of Duisburg-Essen , Essen , Germany.
Nicole MeissnerInstitute for Cell Biology (Cancer Research), University Hospital Essen, University of Duisburg-Essen , Essen , Germany.
Veronika KleffInstitute of Anatomy, University Hospital, University of Duisburg-Essen , Essen , Germany.
Holger JastrowInstitute of Anatomy, University Hospital, University of Duisburg-Essen , Essen , Germany.
Masahiro YamaguchiDepartment of Physiology, Graduate School of Medicine, University of Tokyo , Tokyo , Japan.
Süleyman ErgünInstitute of Anatomy and Cell Biology, University of Würzburg , Würzburg , Germany.
Verena JendrossekInstitute for Cell Biology (Cancer Research), University Hospital Essen, University of Duisburg-Essen , Essen , Germany.
University of Duisburg-Essen · DEThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor vessels with resistance to anti-angiogenic therapy are characterized by the normalization of the vascular structures through integration of mature pericytes and smooth muscle cells (SMC) into the vessel wall, a process termed vessel stabilization. Unfortunately, stabilization-associated vascular remodeling can result in reduced sensitivity to subsequent anti-angiogenic therapy. We show here that blockade of VEGF by bevacizumab induces stabilization of angiogenic tumor blood vessels in human tumor specimen by recruiting Nestin-positive cells, whereas mature vessels down-regulated Nestin-expression. Using xenograft tumors growing on bone-marrow (BM) chimera of C57Bl/6 wildtype and Nestin-GFP transgenic mice, we show for first time that Nestin(+) cells inducing the maturation of tumor vessels do not originate from the BM but presumably reside within the adventitia of adult blood vessels. Complementary ex vivo experiments using explants of murine aortas revealed that Nestin(+) multipotent stem cells (MPSCs) are mobilized from their niche and differentiated into pericytes and SMC through the influence of tumor-cell-secreted factors. We conclude that tissue-resident Nestin(+) cells are more relevant than BM-derived cells for vessel stabilization and therefore have to be considered in future strategies for anti-angiogenic therapy. The identification of proteins mediating recruitment or differentiation of local Nestin(+) cells with potential stem cell character to angiogenic blood vessels may allow the definition of new therapeutic targets to reduce tumor resistance against anti-angiogenic drugs.

Indexed as

mesenchymal stem cellnestinpericytesvascular remodelingvessel maturation

Identifiers

PMID25019063
PMCPMC4072089
OpenAlexW2015719752

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.