Evidence map›Paper›PMID 35434136›Full record

ArticleBioMed research international2022

The Neurokinin-1 Receptor Is Essential for the Viability of Human Glioma Cells: A Possible Target for Treating Glioblastoma.

Mario F Muñoz, Sandro Argüelles, Marisa Rosso, Rafael Medina, Rafael Coveñas, Antonio Ayala, Miguel Muñoz

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Glioma and Peptidergic Systems: Oncogenic and Anticancer Peptides.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  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

7 authors at 3 institutions in 1 country.

Mario F MuñozDepartment of Biochemistry and Molecular Biology, University of Seville, Seville, Spain.ORCID https://orcid.org/0000-0001-7354-2888
Sandro ArgüellesDepartment of Physiology, University of Seville, Seville, Spain.ORCID https://orcid.org/0000-0001-8450-3227
Marisa RossoVirgen del Rocío, University Hospital, Research Laboratory on Neuropeptides (IBIS), Seville, Spain.ORCID https://orcid.org/0000-0001-7587-0025
Rafael MedinaDepartment of Biochemistry and Molecular Biology, University of Seville, Seville, Spain.ORCID https://orcid.org/0000-0003-1876-9961
Rafael CoveñasInstitute of Neurosciences of Castilla Y León (INCYL), Laboratory of Neuroanatomy of the Peptidergic Systems, University of Salamanca, Salamanca, Spain.ORCID https://orcid.org/0000-0001-5677-8266
Antonio AyalaDepartment of Biochemistry and Molecular Biology, University of Seville, Seville, Spain.ORCID https://orcid.org/0000-0001-9711-3711
Miguel MuñozVirgen del Rocío, University Hospital, Research Laboratory on Neuropeptides (IBIS), Seville, Spain.ORCID https://orcid.org/0000-0002-2853-8481
Instituto de Biomedicina de Sevilla · ESUniversidad de Sevilla · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glioblastoma or glioma is the most common malignant brain tumor. Patients have a prognosis of approximately 15 months, despite the current aggressive treatment. Neurokinin-1 receptor (NK-1R) occurs naturally in human glioma, and it is necessary for the tumor development. Objective: The purpose of the study was to increase the knowledge about the involvement of the substance P (SP)/NK-1R system in human glioma. Methods: Cellular localization of NK-1R and SP was studied in GAMG and U-87 MG glioma cell lines by immunofluorescence. The contribution of both SP and NK-1R to the viability of these cells was also assessed after applying the tachykinin 1 receptor ( Results: Both SP and the NK-1R (full-length and truncated isoforms) were localized in the nucleus and cytoplasm of GAMG and U-87 MG glioma cells. The presence of full-length NK-1R isoform was mainly observed in the nucleus, while the level of truncated isoform was higher in the cytoplasm. Cell proliferation was decreased when glioma cells were transfected with Conclusions: Our results show for the first time that the expression of the

Indexed as

GlioblastomaGliomaHumansNeurokinin-1 Receptor AntagonistsProtein IsoformsReceptors, Neurokinin-1RNA, Small InterferingSubstance PNeurokinin-1 Receptor AntagonistsProtein IsoformsReceptors, Neurokinin-1RNA, Small InterferingSubstance PTACR1 protein, human

Identifiers

PMID35434136
PMCPMC9006081
OpenAlexW4226288011

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.