Evidence map›Paper›PMID 31710309›Full record

ArticleThe Journal of clinical investigation2019

Destress and do not suppress: targeting adrenergic signaling in tumor immunosuppression.

Ignacio Iñigo-Marco, Marta M Alonso

Abstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
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  7. Dissecting the role of cell signaling versus CD8Journal of molecular medicine (Berlin, Germany) · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. The updated landscape of tumor microenvironment and drug repurposing.Signal transduction and targeted therapy · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Ignacio Iñigo-MarcoNavarra's Health Research Institute (IDISNA) Pamplona, Spain.
Marta M AlonsoNavarra's Health Research Institute (IDISNA) Pamplona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-induced immunosuppression is a common obstacle for cancer treatment. Adrenergic signaling triggered by chronic stress participates in the creation of an immunosuppressive microenvironment by promoting myeloid-derived suppressor cell (MDSC) proliferation and activation. In this issue of the JCI, Mohammadpour et al. elegantly delve into the mechanisms underlying MDSC contribution to tumor development. They used in vitro and in vivo mouse models to demonstrate that chronic stress results in MDSC accumulation, survival, and immune-inhibitory activity. Of therapeutic relevance, the authors showed that propranolol, a commonly prescribed β-blocker, can reduce MDSC immunosuppression and enhance the effect of other cancer therapies.

Indexed as

NeoplasmsAdrenergic AgentsAnimalsImmunosuppression TherapyMiceMyeloid CellsMyeloid-Derived Suppressor CellsReceptors, Adrenergic, beta-2Tumor MicroenvironmentAdrenergic AgentsReceptors, Adrenergic, beta-2

Identifiers

PMID31710309
PMCPMC6877329

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.