Evidence map›Paper›PMID 32354122›Full record

ReviewInternational journal of molecular sciences2020

TLR-4 Signaling vs. Immune Checkpoints, miRNAs Molecules, Cancer Stem Cells, and Wingless-Signaling Interplay in Glioblastoma Multiforme-Future Perspectives.

Jakub Litak, Cezary Grochowski, Joanna Litak, Ida Osuchowska, Krzysztof Gosik, Elżbieta Radzikowska, Piotr Kamieniak, Jacek Rolinski

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Jakub LitakDepartment of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, 20-954 Lublin, Poland.ORCID 0000-0001-7954-9263
Cezary GrochowskiDepartment of Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.ORCID 0000-0002-2938-885X
Joanna LitakSt. John's Cancer Center in Lublin, 20-090 Lublin, Poland.
Ida OsuchowskaDepartment of Anatomy, Medical University of Lublin, 20-090 Lublin, Poland.
Krzysztof GosikDepartment of Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
Elżbieta RadzikowskaMSWiA Hospital, 02-507 Warsaw, Poland.
Piotr KamieniakDepartment of Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
Jacek RolinskiDepartment of Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
Medical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like-receptor (TLR) family members were detected in the central nervous system (CNS). TLR occurrence was noticed and widely described in glioblastomamultiforme (GBM) cells. After ligand attachment, TLR-4 reorients domains and dimerizes, activates an intracellular cascade, and promotes further cytoplasmatic signaling. There is evidence pointing at a strong relation between TLR-4 signaling and micro ribonucleic acid (miRNA) expression. The TLR-4/miRNA interplay changes typical signaling and encourages them to be a target for modern immunotherapy. TLR-4 agonists initiate signaling and promote programmed death ligand-1 (PD-1L) expression. Most of those molecules are intensively expressed in the GBM microenvironment, resulting in the autocrine induction of regional immunosuppression. Another potential target for immunotreatment is connected with limited TLR-4 signaling that promotes Wnt/DKK-3/claudine-5 signaling, resulting in a limitation of GBM invasiveness. Interestingly, TLR-4 expression results in bordering proliferative trends in cancer stem cells (CSC) and GBM. All of these potential targets could bring new hope for patients suffering from this incurable disease. Clinical trials concerning TLR-4 signaling inhibition/promotion in many cancers are recruiting patients. There is still a lot to do in the field of GBM immunotherapy.

Indexed as

Brain NeoplasmsClinical Trials as TopicGene Expression Regulation, NeoplasticGlioblastomaHumansImmune Checkpoint ProteinsImmunotherapyMicroRNAsNeoplastic Stem CellsSignal TransductionToll-Like Receptor 4Wnt ProteinsImmune Checkpoint ProteinsMicroRNAsTLR4 protein, humanToll-Like Receptor 4Wnt Proteinsglioblastoma multiformegliomahigh-grade gliomaTLRTLR-4toll-like receptor

Identifiers

PMID32354122
PMCPMC7247696
OpenAlexW3021811219

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.