Evidence map›Paper›PMID 25190142›Full record

ReviewCell death and differentiation2015

New insights into IL-12-mediated tumor suppression.

S Tugues, S H Burkhard, I Ohs, M Vrohlings, K Nussbaum, J Vom Berg, P Kulig, B Becher

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 323 papers.

0numbers the graph read from it
0cells of the map it votes in
323citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

323 citing papers in PubMed, 543 citations in OpenAlex.

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263 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

8 authors at 1 institution in 1 country.

S TuguesInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
S H BurkhardInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
I OhsInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
M VrohlingsInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
K NussbaumInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
J Vom BergInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
P KuligInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
B BecherInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
University of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past two decades, interleukin-12 (IL-12) has emerged as one of the most potent cytokines in mediating antitumor activity in a variety of preclinical models. Through pleiotropic effects on different immune cells that form the tumor microenvironment, IL-12 establishes a link between innate and adaptive immunity that involves different immune effector cells and cytokines depending on the type of tumor or the affected tissue. The robust antitumor response exerted by IL-12, however, has not yet been successfully translated into the clinics. The majority of clinical trials involving treatment with IL-12 failed to show sustained antitumor responses and were associated to toxic side effects. Here we discuss the therapeutic effects of IL-12 from preclinical to clinical studies, and will highlight promising strategies to take advantage of the antitumor activity of IL-12 while limiting adverse effects.

Indexed as

AnimalsDisease Models, AnimalHumansImmunosuppressive AgentsInterleukin-12MiceNeoplasmsImmunosuppressive AgentsInterleukin-12

Identifiers

PMID25190142
PMCPMC4291488
OpenAlexW2082554712

What OpenQuestion holds

Textmetadata
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.