Evidence map›Paper›PMID 31616440›Full record

ReviewFrontiers in immunology2019

NK Cell Metabolism and Tumor Microenvironment.

Iñigo Terrén, Ane Orrantia, Joana Vitallé, Olatz Zenarruzabeitia, Francisco Borrego

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 335 papers.

0numbers the graph read from it
0cells of the map it votes in
335citing papers in PubMed
–field-weighted citation impact
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

335 citing papers in PubMed.

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  18. Resident CD49aScience advances · 2026
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275 more citing papers are in PubMed but not listed here.

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

5 authors.

Iñigo TerrénImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Ane OrrantiaImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Joana VitalléImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Olatz ZenarruzabeitiaImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Francisco BorregoImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural Killer (NK) cells are characterized by their potential to kill tumor cells by different means without previous sensitization and have, therefore, become a valuable tool in cancer immunotherapy. However, their efficacy against solid tumors is still poor and further studies are required to improve it. One of the major restrictions for NK cell activity is the immunosuppressive tumor microenvironment (TME). There, tumor and other immune cells create the appropriate conditions for tumor proliferation while, among others, preventing NK cell activation. Furthermore, NK cell metabolism is impaired in the TME, presumably due to nutrient and oxygen deprivation, and the higher concentration of tumor-derived metabolic end products, such as lactate. This metabolic restriction of NK cells limits their effector functions, and it could represent a potential target to focus on to improve the efficacy of NK cell-based therapies against solid tumors. In this review, we discuss the potential effect of TME into NK cell metabolism and its influence in NK cell effector functions.

Indexed as

AnimalsCell ProliferationHumansImmune ToleranceImmunotherapyKiller Cells, NaturalLymphocyte ActivationNeoplasmsTumor Microenvironmentamino acidglucoseglycolysishypoxiametabolismNK cellTMEtumor microenvironment

Identifiers

PMID31616440
PMCPMC6769035

What OpenQuestion holds

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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.