Evidence map›Paper›PMID 29316666›Full record

ReviewInternational journal of molecular sciences2018

Fusion Proteins of NKG2D/NKG2DL in Cancer Immunotherapy.

Hui Ding, Xi Yang, Yanzhang Wei

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  8. Chimeric Antigen Receptor Design and Efficacy in Ovarian Cancer Treatment.International journal of molecular sciences · 2021
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  15. Accelerator or Brake: Immune Regulators in Malaria.Frontiers in cellular and infection microbiology · 2020
    Review
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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

3 authors at 1 institution in 1 country.

Hui DingDepartment of Biological Sciences, Clemson University, 190 Collings Street, Clemson, SC 29634, USA. ding4@clemson.edu.ORCID 0000-0002-2277-3894
Xi YangDepartment of Biological Sciences, Clemson University, 190 Collings Street, Clemson, SC 29634, USA. xiy@clemson.edu.
Yanzhang WeiDepartment of Biological Sciences, Clemson University, 190 Collings Street, Clemson, SC 29634, USA. ywei@clemson.edu.ORCID 0000-0001-6942-095X
Clemson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NKG2D (natural killer group 2, member D) is an important activating receptor in natural killer (NK) cells and some T cells. NKG2D ligands (NKG2DLs) are specifically expressed on most tumor cells. The engagement of these ligands on tumor cells to NKG2D on NK cells will induce cell-mediated cytotoxicity and have target cells destroyed. This gives NKG2D/NKG2DLs great potential in cancer therapeutic application. The creation of NKG2D/NKG2DL-based multi-functional fusion proteins is becoming one of the most promising strategies in immunotherapy for cancer. Antibodies, cytokines, and death receptors have been fused with NKG2D or its ligands to produce many powerful fusion proteins, including NKG2D-based chimeric antigen receptors (CARs). In this article, we review the recent developments of the fusion proteins with NKG2D/NKG2DL ligands in cancer immunotherapy.

Indexed as

AnimalsAntibodiesCytokinesGPI-Linked ProteinsHumansImmunotherapyIntercellular Signaling Peptides and ProteinsNeoplasmsNK Cell Lectin-Like Receptor Subfamily KRecombinant Fusion ProteinsAntibodiesCytokinesGPI-Linked ProteinsIntercellular Signaling Peptides and ProteinsKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily KRecombinant Fusion ProteinsULBP2 protein, humancancer immunotherapyfusion proteinNKG2DNKG2D CARsNKG2D ligands

Identifiers

PMID29316666
PMCPMC5796126
OpenAlexW2787249384

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.