Evidence map›Paper›PMID 24875217›Full record

ReviewCell cycle (Georgetown, Tex.)2014

E3 ubiquitin ligase Cbl-b in innate and adaptive immunity.

Qingjun Liu, Hong Zhou, Wallace Y Langdon, Jian Zhang

Abstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Possible Trace of HTLV-1 Virus in Modulation of Cbl-b, ITCH, and PP2A Suppressor Genes.International journal of molecular and cellular medicine · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Facts and Hopes in Using Omics to Advance Combined Immunotherapy Strategies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Targeting Cbl-b in cancer immunotherapy.Journal for immunotherapy of cancer · 2023
    Review
  16. Article
  17. Article
  18. Tumor rejection inJournal for immunotherapy of cancer · 2021
    Article
  19. Review
  20. Cell Cycle Entry Control in Naïve and Memory CD8Frontiers in cell and developmental biology · 2021
    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

4 authors.

Qingjun LiuLaboratory of Immunohematology; Beijing Institute of Transfusion Medicine; Beijing, PR China; Department of Microbial Infection and Immunity; The Ohio State University; Columbus, OH USA.
Hong ZhouLaboratory of Immunohematology; Beijing Institute of Transfusion Medicine; Beijing, PR China.
Wallace Y LangdonSchool of Pathology and Laboratory Medicine; University of Western Australia; Crawley, Western Australia, Australia.
Jian ZhangDepartment of Microbial Infection and Immunity; The Ohio State University; Columbus, OH USA.

Funding

NEDD4 IN T HELPER CELL DEVELOPMENT AND AUTOIMMUNITYR01AI090901 · NIAID · UNIVERSITY OF IOWA · PI WALDSCHMIDT, THOMAS J · 2010 to 2020
$4.0M
NIAID NIH HHS R01 AI090901NIAID NIH HHS R01AI090901
6 · The paper itself

Abstract

Casitas B-lineage lymphoma proto-oncogene-b (Cbl-b), a RING finger E3 ubiquitin-protein ligase, has been demonstrated to play a crucial role in establishing the threshold for T-cell activation and controlling peripheral T-cell tolerance via multiple mechanisms. Accumulating evidence suggests that Cbl-b also regulates innate immune responses and plays an important role in host defense to pathogens. Understanding the signaling pathways regulated by Cbl-b in innate and adaptive immune cells is therefore essential for efficient manipulation of Cbl-b in emerging immunotherapies for human disorders such as autoimmune diseases, allergic inflammation, infections, and cancer. In this article, we review the latest developments in the molecular structural basis of Cbl-b function, the regulation of Cbl-b expression, the signaling mechanisms of Cbl-b in immune cells, as well as the biological function of Cbl-b in physiological and pathological immune responses in animal models and human diseases.

Indexed as

Adaptive ImmunityAdaptor Proteins, Signal TransducingAnimalsAutoimmune DiseasesHumansImmunity, InnateImmunotherapyInflammationNeoplasmsOrgan SpecificityProtein ConformationProto-Oncogene MasProto-Oncogene Proteins c-cblSignal TransductionUbiquitin-Protein LigasesAdaptor Proteins, Signal TransducingCBLB protein, humanMAS1 protein, humanProto-Oncogene MasProto-Oncogene Proteins c-cblUbiquitin-Protein Ligasesbiological functionCbl-bimmune disease and therapymolecular structionsignaling mechanism

Identifiers

PMID24875217
PMCPMC4111751

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.