Evidence map›Paper›PMID 32737988›Full record

ReviewBritish journal of pharmacology2020

NKp30 - A prospective target for new cancer immunotherapy strategies.

Pedro F Pinheiro, Gonçalo C Justino, M Matilde Marques

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.9field-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

33 citing papers in PubMed, 46 citations in OpenAlex.

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  20. Identification and Characterization of CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    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

3 authors at 1 institution in 1 country.

Pedro F PinheiroCentro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Lisbon, Portugal.
Gonçalo C JustinoCentro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Lisbon, Portugal.
M Matilde MarquesCentro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa, Lisbon, Portugal.
University of Lisbon · PT

Funding

Fundação para a Ciência e a Tecnologia PTDC/QUI-QAN/32242/2017Fundação para a Ciência e a Tecnologia SAICTPAC/0019/2015Fundação para a Ciência e a Tecnologia SFRH/BD/110945/2015Fundação para a Ciência e a Tecnologia UIDB/00100/2020Liga Portuguesa Contra o Cancro LPCC/NRS-Terry Fox grant 2015-2017
6 · The paper itself

Abstract

Natural killer (NK) cells are an important arm of the innate immune system. They constitutively express the NKp30 receptor. NKp30-mediated responses are triggered by the binding of specific ligands e.g. tumour cell-derived B7-H6 and involve the secretion of cytotoxic mediators including TNF-α, IFN-γ, perforins and granzymes. The latter two constitute a target cell-directed response that is critical in the process of immunosurveillance. The structure of NKp30 is presented, focusing on the ligand-binding site, on the ligand-induced structural changes and on the experimental data available correlating structure and binding affinity. The translation of NKp30 structural changes to disease progression is also reviewed. NKp30 role in immunotherapy has been explored in chimeric antigen receptor T-cell (CAR-T) therapy. However, antibodies or small ligands targeting NKp30 have not yet been developed. The data reviewed herein unveil the key structural aspects that must be considered for drug design in order to develop novel immunotherapy approaches.

Indexed as

NeoplasmsAnimalsHumansImmunotherapyKiller Cells, NaturalNatural Cytotoxicity Triggering Receptor 3Prospective StudiesNatural Cytotoxicity Triggering Receptor 3NCR3 protein, humanantigen recognition receptors, ligands, cancer, and carcinogenesiscancer pharmacologyimmunopharmacology

Identifiers

PMID32737988
PMCPMC7520444
OpenAlexW3046428885

What OpenQuestion holds

Textmetadata
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.