Evidence map›Paper›PMID 24711808›Full record

ReviewFrontiers in immunology2014

Molecular Bases for the Regulation of NKG2D Ligands in Cancer.

Leticia Huergo-Zapico, Andrea Acebes-Huerta, Alejandro López-Soto, Mónica Villa-Álvarez, Ana Pilar Gonzalez-Rodriguez, Segundo Gonzalez

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.3field-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

36 citing papers in PubMed, 63 citations in OpenAlex.

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  20. Sensing Bacterial-Induced DNA Damaging EffectsFrontiers in immunology · 2018
    Review
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

6 authors at 2 institutions in 1 country.

Leticia Huergo-ZapicoDepartment of Functional Biology, University Institute of Oncology (IUOPA), University of Oviedo , Oviedo , Spain.
Andrea Acebes-HuertaDepartment of Functional Biology, University Institute of Oncology (IUOPA), University of Oviedo , Oviedo , Spain.
Alejandro López-SotoDepartment of Functional Biology, University Institute of Oncology (IUOPA), University of Oviedo , Oviedo , Spain.
Mónica Villa-ÁlvarezDepartment of Functional Biology, University Institute of Oncology (IUOPA), University of Oviedo , Oviedo , Spain.
Ana Pilar Gonzalez-RodriguezDepartment of Hematology, Hospital Universitario Central de Asturias , Oviedo , Spain.
Segundo GonzalezDepartment of Functional Biology, University Institute of Oncology (IUOPA), University of Oviedo , Oviedo , Spain.
Universidad de Oviedo · ESHospital Universitario Central de Asturias · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NKG2D is an activating receptor expressed by NK and T cells primarily involved in the elimination of transformed and infected cells. NKG2D ligands are self-proteins restrictedly expressed in healthy tissues, but induced in response to signaling pathways commonly associated with transformation. Proliferative, tumor suppressor, and stress signaling pathways linked to the tumorigenic process induce the expression of NKG2D ligands, initiating an immune response against the incipient tumor. Nevertheless, the activity of NKG2D ligands is counter-regulated in vivo by the immunoediting of cancer cells, resulting in the expression of multiple mechanisms of immune evasion in advanced tumors. The redundancy of NKG2D ligands, besides increasing the complexity of their regulation, may impair the generation of these immune evasion mechanisms. In this review, we attempt to integrate the mechanisms and pathways involved in the regulation of NKG2D ligand expression in cancer.

Indexed as

MICAMICBNK cellNKG2Dregulationsignaling pathwaysT cellsULBP

Identifiers

PMID24711808
PMCPMC3968767
OpenAlexW2114029170

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.