Evidence map›Paper›PMID 33362756›Full record

ReviewFrontiers in immunology2020

The Murine CD137/CD137 Ligand Signalosome: A Signal Platform Generating Signal Complexity.

Beom K Choi, Hyeon-Woo Lee

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 4-1BB immunotherapy: advances and hurdles.Experimental & molecular medicine · 2024
    Review
  5. Identification of a distinct cluster of GDF15Frontiers in immunology · 2024
    Article
  6. Isotype-specific plasma cells express divergent transcriptional programs.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Role of ADAM10 and ADAM17 in Regulating CD137 Function.International journal of molecular sciences · 2021
    Article
  9. 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

2 authors at 2 institutions in 1 country.

Beom K ChoiBiomedicine Production Branch, Program for Immunotherapy Research, National Cancer Center, Goyang, South Korea.
Hyeon-Woo LeeDepartment of Pharmacology, School of Dentistry, Graduate School, Institute of Oral Biology, Kyung Hee University, Seoul, South Korea.
Kyung Hee University · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD137, a member of the TNFR family, is a costimulatory receptor, and CD137L, a member of the TNF family, is its ligand. Studies using CD137- and CD137L-deficient mice and antibodies against CD137 and CD137L have revealed the diverse and paradoxical effects of these two proteins in various cancers, autoimmunity, infections, and inflammation. Both their cellular diversity and their spatiotemporal expression patterns indicate that they mediate complex immune responses. This intricacy is further enhanced by the bidirectional signal transduction events that occur when these two proteins interact in various types of immune cells. Here, we review the biology of murine CD137/CD137L, particularly, the complexity of their proximal signaling pathways, and speculate on their roles in immune responses.

Indexed as

4-1BB LigandAnimalsMiceSignal TransductionTumor Necrosis Factor Receptor Superfamily, Member 94-1BB LigandTnfrsf9 protein, mouseTnfsf9 protein, mouseTumor Necrosis Factor Receptor Superfamily, Member 9bi-directional signal transduction pathwaysCD137CD137/CD137L-mediated immune modulationCD137 ligandsignalosome

Identifiers

PMID33362756
PMCPMC7758191
OpenAlexW3111861873

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.