Evidence map›Paper›PMID 30567306›Full record

ReviewCancers2018

NK Cell-Based Glioblastoma Immunotherapy.

Irene Golán, Laura Rodríguez de la Fuente, Jose A Costoya

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. NKG2C/Journal for immunotherapy of cancer · 2024
    Article
  10. Current approaches in glioblastoma multiforme immunotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  11. Article
  12. The TGF-β Family in Glioblastoma.International journal of molecular sciences · 2024
    Review
  13. Targeting Innate Immunity in Glioma Therapy.International journal of molecular sciences · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  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

3 authors at 1 institution in 1 country.

Irene GolánMolecular Oncology Laboratory MOL, Departamento de Fisioloxia, CiMUS, Facultade de Medicina, Universidade de Santiago de Compostela, IDIS, 15782 Santiago de Compostela, Spain. irene.golan@usc.es.ORCID 0000-0003-3982-8748
Laura Rodríguez de la FuenteMolecular Oncology Laboratory MOL, Departamento de Fisioloxia, CiMUS, Facultade de Medicina, Universidade de Santiago de Compostela, IDIS, 15782 Santiago de Compostela, Spain. lau.gz21@gmail.com.ORCID 0000-0003-1194-7024
Jose A CostoyaMolecular Oncology Laboratory MOL, Departamento de Fisioloxia, CiMUS, Facultade de Medicina, Universidade de Santiago de Compostela, IDIS, 15782 Santiago de Compostela, Spain. josea.costoya@usc.es.ORCID 0000-0003-3691-6419
Universidade de Santiago de Compostela · ES

Funding

REGULATION OF EPIDERMAL GROWTH FACTOR RECEPTOR GENEF32CA008629 · NCI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI HUDSON, LAURIE G · 1988 to 1990
–
Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia GPC2014/030Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia PRE/2011/131Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia PXIB208091PREuropean Regional Development Fund ED431G/05Ministerio de Ciencia e Innovación SAF2008-00543Ministerio de Ciencia e Innovación SAF2009-08629Ministerio de Economía y Competitividad PI15/01129
6 · The paper itself

Abstract

Glioblastoma (GB) is the most aggressive and most common malignant primary brain tumor diagnosed in adults. GB shows a poor prognosis and, unfortunately, current therapies are unable to improve its clinical outcome, imposing the need for innovative therapeutic approaches. The main reason for the poor prognosis is the great cell heterogeneity of the tumor mass and its high capacity for invading healthy tissues. Moreover, the glioblastoma microenvironment is capable of suppressing the action of the immune system through several mechanisms such as recruitment of cell modulators. Development of new therapies that avoid this immune evasion could improve the response to the current treatments for this pathology. Natural Killer (NK) cells are cellular components of the immune system more difficult to deceive by tumor cells and with greater cytotoxic activity. Their use in immunotherapy gains strength because they are a less toxic alternative to existing therapy, but the current research focuses on mimicking the NK attack strategy. Here, we summarize the most recent studies regarding molecular mechanisms involved in the GB and immune cells interaction and highlight the relevance of NK cells in the new therapeutic challenges.

Indexed as

brain tumorglioblastomaimmunotherapymalignant gliomasNK cells

Identifiers

PMID30567306
PMCPMC6315402
OpenAlexW2905145431

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.