Evidence map›Paper›PMID 32082316›Full record

ArticleFrontiers in immunology2020

Boosting Natural Killer Cell-Mediated Targeting of Sarcoma Through DNAM-1 and NKG2D.

Ece Canan Sayitoglu, Anna-Maria Georgoudaki, Michael Chrobok, Didem Ozkazanc, Benjamin J Josey, Muhammad Arif, Kim Kusser, Michelle Hartman, Tamara M Chinn, Renee Potens and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

43 citing papers in PubMed, 55 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

18 authors at 8 institutions in 4 countries.

Ece Canan SayitogluDr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, United States.
Anna-Maria GeorgoudakiDr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, United States.
Michael ChrobokCenter for Hematology and Regenerative Medicine, Karolinska University Hospital Huddinge, Karolinska Institutet, Stockholm, Sweden.
Didem OzkazancFaculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.
Benjamin J JoseyDr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, United States.
Muhammad ArifScience for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden.
Kim KusserTranslational Research and Economic Development, Nova Southeastern University, Fort Lauderdale, FL, United States.
Michelle HartmanTranslational Research and Economic Development, Nova Southeastern University, Fort Lauderdale, FL, United States.
Tamara M ChinnDr. Kiran C. Patel College of Osteopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, United States.
Renee PotensNSU Cell Therapy Institute, Nova Southeastern University, Fort Lauderdale, FL, United States.
Cevriye PamukcuFaculty of Engineering and Natural Sciences, Sabanci University, Istanbul, Turkey.
Robin KruegerTranslational Research and Economic Development, Nova Southeastern University, Fort Lauderdale, FL, United States.
Cheng ZhangFaculty of Dentistry, Oral & Craniofacial Sciences, Centre for Host-Microbiome Interactions, King's College London, London, United Kingdom.
Adil MardinogluScience for Life Laboratory, KTH Royal Institute of Technology, Stockholm, Sweden.
Evren AliciCenter for Hematology and Regenerative Medicine, Karolinska University Hospital Huddinge, Karolinska Institutet, Stockholm, Sweden.
Harry Thomas TempleDepartment of Surgery, Dr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, United States.
Tolga SutluDepartment of Molecular Biology and Genetics, Bogaziçi University, Istanbul, Turkey.
Adil Doganay DuruDr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, FL, United States.
Nova Southeastern University · USKarolinska Institutet · SESabancı Üniversitesi · TRBoğaziçi University · TRKarolinska University Hospital · SEKing's College London · GBKTH Royal Institute of Technology · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcomas are malignancies of mesenchymal origin that occur in bone and soft tissues. Many are chemo- and radiotherapy resistant, thus conventional treatments fail to increase overall survival. Natural Killer (NK) cells exert anti-tumor activity upon detection of a complex array of tumor ligands, but this has not been thoroughly explored in the context of sarcoma immunotherapy. In this study, we investigated the NK cell receptor/ligand immune profile of primary human sarcoma explants. Analysis of tumors from 32 sarcoma patients identified the proliferative marker PCNA and DNAM-1 ligands CD112 and/or CD155 as commonly expressed antigens that could be efficiently targeted by genetically modified (GM) NK cells. Despite the strong expression of CD112 and CD155 on sarcoma cells, characterization of freshly dissociated sarcomas revealed a general decrease in tumor-infiltrating NK cells compared to the periphery, suggesting a defect in the endogenous NK cell response. We also applied a functional screening approach to identify relevant NK cell receptor/ligand interactions that induce efficient anti-tumor responses using a panel NK-92 cell lines GM to over-express 12 different activating receptors. Using GM NK-92 cells against primary sarcoma explants (

Indexed as

TransgenesAdolescentAdultAgedAged, 80 and overAntigens, Differentiation, T-LymphocyteCell- and Tissue-Based TherapyCell DegranulationCell Line, TumorChildChild, PreschoolCytotoxicity, ImmunologicGenetic VectorsHumansImmunotherapy, AdoptiveInfantAntigens, Differentiation, T-LymphocyteKLRK1 protein, humanLigandsNK Cell Lectin-Like Receptor Subfamily Kpoliovirus receptorPVRIG protein, humanReceptors, Cell SurfaceReceptors, VirusT Lineage-Specific Activation Antigen 1cancer immunologycancer immunotherapyDNAM-1 (CD226)natural killer (NK) cellNK-92 cell lineNKG2D (Natural killer group 2 member D)sarcoma

Identifiers

PMID32082316
PMCPMC7001093
OpenAlexW3004130920

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.