Evidence map›Paper›PMID 31412671›Full record

ReviewCancers2019

Interactions of Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (TRAIL) with the Immune System: Implications for Inflammation and Cancer.

Katharina Beyer, Ann-Kathrin Baukloh, Ani Stoyanova, Carsten Kamphues, Arne Sattler, Katja Kotsch

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

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  14. Neutrophils: Many Ways to Die.Frontiers in immunology · 2021
    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

6 authors at 1 institution in 1 country.

Katharina BeyerCharité-Universitätsmedizin Berlin, Department of General, Visceral and Vascular Surgery, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany. katharina.beyer2@charite.de.
Ann-Kathrin BauklohCharité-Universitätsmedizin Berlin, Department of General, Visceral and Vascular Surgery, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Ani StoyanovaCharité-Universitätsmedizin Berlin, Department of General, Visceral and Vascular Surgery, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Carsten KamphuesCharité-Universitätsmedizin Berlin, Department of General, Visceral and Vascular Surgery, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Arne SattlerCharité-Universitätsmedizin Berlin, Department of General, Visceral and Vascular Surgery, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Katja KotschCharité-Universitätsmedizin Berlin, Department of General, Visceral and Vascular Surgery, Campus Benjamin Franklin, Hindenburgdamm 30, 12203 Berlin, Germany.
Charité - Universitätsmedizin Berlin · DE

Funding

Deutsche Forschungsgemeinschaft BE 5515/6-1
6 · The paper itself

Abstract

Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a member of the TNF superfamily. TRAIL has historically been distinct from the Fas ligand and TNFα in terms of selective apoptosis induction in tumor cells and has a nearly non-existent systemic toxicity. Consequently, in the search for an ideal drug for tumor therapy, TRAIL rapidly drew interest, promising effective tumor control with minimal side effects. However, euphoria gave way to disillusionment as it turned out that carcinoma cells possess or can acquire resistance to TRAIL-induced apoptosis. Additionally, studies on models of inflammation and autoimmunity revealed that TRAIL can influence immune cells in many different ways. While TRAIL was initially found to be an important player in tumor defense by natural killer cells or cytotoxic T cells, additional effects of TRAIL on regulatory T cells and effector T cells, as well as on neutrophilic granulocytes and antigen-presenting cells, became focuses of interest. The tumor-promoting effects of these interactions become particularly important for consideration in cases where tumors are resistant to TRAIL-induced apoptosis. Consequently, murine models have shown that TRAIL can impair the tumor microenvironment toward a more immunosuppressive type, thereby promoting tumor growth. This review summarizes the current state of knowledge on TRAIL's interactions with the immune system in the context of cancer.

Indexed as

TRAIL, apoptosis, cancer, inflammation, immune system

Identifiers

PMID31412671
PMCPMC6721490
OpenAlexW2968247753

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.