Evidence map›Paper›PMID 31143450›Full record

ArticlePharmacology research & perspectives2019

Histidine-rich glycoprotein augments natural killer cell function by modulating PD-1 expression via CLEC-1B.

Yoshito Nishimura, Hidenori Wake, Kiyoshi Teshigawara, Dengli Wang, Masakiyo Sakaguchi, Fumio Otsuka, Masahiro Nishibori

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 14 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

7 authors at 1 institution in 1 country.

Yoshito NishimuraDepartment of Pharmacology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.ORCID 0000-0003-0224-7501
Hidenori WakeDepartment of Pharmacology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.
Kiyoshi TeshigawaraDepartment of Pharmacology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.
Dengli WangDepartment of Pharmacology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.
Masakiyo SakaguchiDepartment of Cell Biology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.
Fumio OtsukaDepartment of General Medicine Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.ORCID 0000-0001-7014-9095
Masahiro NishiboriDepartment of Pharmacology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Okayama Japan.
Okayama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Augmentation of natural killer (NK) cell cytotoxicity is one of the greatest challenges for cancer immunotherapy. Although histidine-rich glycoprotein (HRG), a 75-kDa glycoprotein with various immunomodulatory activities, reportedly elicits antitumor immunity, its effect on NK cell cytotoxicity is unclear. We assessed NK cell cytotoxicity against K562 cells. We also measured concentrations of cytokines and granzyme B in the cell supernatant. The proportion of CD56

Indexed as

ActinsCD56 AntigenCell NucleusCells, CulturedCell SurvivalGranzymesHistidine-Rich GlycoproteinHumansImmunotherapyK562 CellsKiller Cells, NaturalLectins, C-TypeNeoplasmsProgrammed Cell Death 1 ReceptorProteinsActinsCD56 AntigenCLEC1B protein, humanGranzymesGZMB protein, humanHistidine-Rich GlycoproteinLectins, C-TypeNCAM1 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 ReceptorProteinsC‐type lectin‐like receptorhistidine‐rich glycoproteinnatural killer cellprogrammed‐death‐1

Identifiers

PMID31143450
PMCPMC6531599
OpenAlexW2945410190

What OpenQuestion holds

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LicenceCC BY
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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.