Evidence map›Paper›PMID 34521765›Full record

ArticleMolecular cancer research : MCR2021

Adenosine A2A Receptor Activation Enhances Blood-Tumor Barrier Permeability in a Rodent Glioma Model.

Amélie Vézina, Monica Manglani, DreeAnna Morris, Brandon Foster, Matthew McCord, Hua Song, Meili Zhang, Dionne Davis, Wei Zhang, Jessica Bills and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. 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

20 authors at 5 institutions in 1 country.

Amélie VézinaNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.
Monica ManglaniViral Immunology and Intravital Imaging Section, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, Maryland.
DreeAnna MorrisDepartment of Neurology, Oregon Health & Sciences University, Portland, Oregon.ORCID 0000-0001-7276-3865
Brandon FosterSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, Maryland.
Matthew McCordNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.ORCID 0000-0001-7673-4463
Hua SongNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.
Meili ZhangNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.
Dionne DavisNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.
Wei ZhangNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.
Jessica BillsDepartment of Neurology, Oregon Health & Sciences University, Portland, Oregon.
Kunio NagashimaElectron Microscope Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, Maryland.
Priya ShankarappaGenitourinary Malignancies Branch, Molecular Pharmacology Section, NCI, NIH, Bethesda, Maryland.ORCID 0000-0002-7173-4808
Jessica KindrickGenitourinary Malignancies Branch, Molecular Pharmacology Section, NCI, NIH, Bethesda, Maryland.
Stuart WalbridgeSurgical Neurology Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, Maryland.
Cody J PeerGenitourinary Malignancies Branch, Molecular Pharmacology Section, NCI, NIH, Bethesda, Maryland.ORCID 0000-0001-9395-3473
William D FiggGenitourinary Malignancies Branch, Molecular Pharmacology Section, NCI, NIH, Bethesda, Maryland.ORCID 0000-0003-2428-5613
Mark R GilbertNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland.ORCID 0000-0003-2556-9722
Dorian B McGavernViral Immunology and Intravital Imaging Section, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, Maryland.ORCID 0000-0001-9568-545X
Leslie L MuldoonDepartment of Neurology, Oregon Health & Sciences University, Portland, Oregon.
Sadhana JacksonNeuro-Oncology Branch, NCI, NIH, Bethesda, Maryland. sadhana.jackson@nih.gov.
National Institutes of Health · USNational Cancer Institute · USNational Institute of Neurological Disorders and Stroke · USLeidos (United States) · USOregon Health & Science University · US

Funding

Modulating BBB Permeability in Malignant GliomaZIANS009417 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI JACKSON, SADHANA · 2020 to 2025
$10.3M
Modulating BBB Permeability in Malignant GliomaZIABC011686 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JACKSON, SADHANA · 2016 to 2019
$1.6M
Intramural NIH HHS Z99 NS999999Intramural NIH HHS ZIA BC011686Intramural NIH HHS ZIA NS009417
6 · The paper itself

Abstract

The blood-tumor barrier (BTB) limits the entry of effective chemotherapeutic agents into the brain for treatment of malignant tumors like glioblastoma. Poor drug entry across the BTB allows infiltrative glioma stem cells to evade therapy and develop treatment resistance. Regadenoson, an FDA-approved adenosine A2A receptor (A2AR) agonist, has been shown to increase drug delivery across the blood-brain barrier in non-tumor-bearing rodents without a defined mechanism of enhancing BTB permeability. Here, we characterize the time-dependent impact of regadenoson on brain endothelial cell interactions and paracellular transport, using mouse and rat brain endothelial cells and tumor models.

Indexed as

AnimalsBlood-Brain BarrierBrain NeoplasmsDisease Models, AnimalFemaleGliomaHumansMiceMice, SCIDRatsRats, NudeReceptor, Adenosine A2ASurvival AnalysisTransfectionReceptor, Adenosine A2A

Identifiers

PMID34521765
PMCPMC8642293
OpenAlexW3201594622

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.