Evidence map›Paper›PMID 29297738›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2018

Periarteriolar Glioblastoma Stem Cell Niches Express Bone Marrow Hematopoietic Stem Cell Niche Proteins.

Vashendriya V V Hira, Jill R Wormer, Hala Kakar, Barbara Breznik, Britt van der Swaan, Renske Hulsbos, Wikky Tigchelaar, Zbynek Tonar, Mohammed Khurshed, Remco J Molenaar and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-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

28 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. New Insights in ATP Synthesis as Therapeutic Target in Cancer and Angiogenic Ocular Diseases.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. AmotL2, IQGAP1, and FKBP51 Scaffold Proteins in Glioblastoma Stem Cell Niches.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2022
    Review
  12. Cell Biology Meets Cell Metabolism: Energy Production Is Similar in Stem Cells and in Cancer Stem Cells in Brain and Bone Marrow.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2022
    Review
  13. Repurposing of Anticancer Stem Cell Drugs in Brain Tumors.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  14. Proteases Regulate Cancer Stem Cell Properties and Remodel Their Microenvironment.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Review
  15. Article
  16. Immunohistochemical Detection of Neural Stem Cells and Glioblastoma Stem Cells in the Subventricular Zone of Glioblastoma Patients.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Article
  17. Review
  18. Review
  19. Review
  20. Cancers · 2020
    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

11 authors at 3 institutions in 3 countries.

Vashendriya V V HiraDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Jill R WormerDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Hala KakarDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Barbara BreznikDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, Ljubljana, Slovenia.
Britt van der SwaanDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Renske HulsbosDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Wikky TigchelaarDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Zbynek TonarDepartment of Histology and Embryology and Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Mohammed KhurshedDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Remco J MolenaarDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Cornelis J F Van NoordenDepartment of Medical Biology, Cancer Center Amsterdam, Academic Medical Center, Amsterdam, The Netherlands.
Academic Medical Center · NLCharles University · CZNational Institute of Biology · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In glioblastoma, a fraction of malignant cells consists of therapy-resistant glioblastoma stem cells (GSCs) residing in protective niches that recapitulate hematopoietic stem cell (HSC) niches in bone marrow. We have previously shown that HSC niche proteins stromal cell-derived factor-1α (SDF-1α), C-X-C chemokine receptor type 4 (CXCR4), osteopontin (OPN), and cathepsin K (CatK) are expressed in hypoxic GSC niches around arterioles in five human glioblastoma samples. In HSC niches, HSCs are retained by binding of SDF-1α and OPN to their receptors CXCR4 and CD44, respectively. Protease CatK cleaves SDF-1α to release HSCs out of niches. The aim of the present study was to reproduce the immunohistochemical localization of these GSC markers in 16 human glioblastoma samples with the addition of three novel markers. Furthermore, we assessed the type of blood vessels associated with GSC niches. In total, we found seven GSC niches containing CD133-positive and nestin-positive GSCs as a single-cell layer exclusively around the tunica adventitia of 2% of the CD31-positive and SMA-positive arterioles and not around capillaries and venules. Niches expressed SDF-1α, CXCR4, CatK, OPN, CD44, hypoxia-inducible factor-1α, and vascular endothelial growth factor. In conclusion, we show that GSC niches are present around arterioles and express bone marrow HSC niche proteins.

Indexed as

Stem Cell NicheAdultAgedArteriolesBrain NeoplasmsCathepsin KChemokine CXCL12GlioblastomaHematopoietic Stem CellsHumansHyaluronan ReceptorsImmunohistochemistryMiddle AgedNeoplastic Stem CellsOsteopontinReceptors, CXCR4Cathepsin KChemokine CXCL12CXCR4 protein, humanHyaluronan ReceptorsOsteopontinReceptors, CXCR4SPP1 protein, humanarteriolesblood vesselsbone marrow nichesglioma stem cellhematopoietic stem cellniches

Identifiers

PMID29297738
PMCPMC5833177
OpenAlexW2781602565

What OpenQuestion holds

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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.