Evidence map›Paper›PMID 12885274›Full record

ReviewExpert opinion on therapeutic targets2003

Cellular FLICE-inhibitory protein: an attractive therapeutic target?

Olivier Micheau

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

53 citing papers in PubMed, 101 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Get Spliced: Uniting Alternative Splicing and Arthritis.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
  10. Early B cell factor 4 modulates FAS-mediated apoptosis and promotes cytotoxic function in human immune cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Mechanisms of Natural Extracts ofInternational journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
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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

1 author at 1 institution in 1 country.

Olivier MicheauINSERM 517, IFR100, Faculty of Medicine, 7 Boulevard Jeanne d'Arc, 21079 Dijon cedex, France. omicheau@u-bourgogne.fr
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular FLIP (c-FLIP), also known as FLICE-inhibitory protein, has been identified as an inhibitor of apoptosis triggered by engagement of death receptors (DRs) such as Fas or TRAIL (TNF-related apoptosis-inducing ligand). cFLIP is recruited to DR signalling complexes, where it prevents caspase activation. Animal models have indicated that c-FLIP plays an important role in T cell proliferation and heart development. Abnormal c-FLIP expression has been identified in various diseases such as multiple sclerosis (MS), Alzheimer's disease (AD), diabetes mellitus, rheumatoid arthritis (RA) and various cancers. This review focuses on recent insights into c-FLIP dysregulation associated with human diseases and addresses the possibilities of using c-FLIP as a therapeutic target.

Indexed as

Drug DesignAlternative SplicingAlzheimer DiseaseAnimalsApoptosisArthritis, RheumatoidAutoimmune DiseasesCardiovascular DiseasesCASP8 and FADD-Like Apoptosis Regulating ProteinDiabetes Mellitus, Type 1Gene Expression RegulationHumansIntracellular Signaling Peptides and ProteinsLymphoproliferative DisordersMiceMice, Inbred NODCASP8 and FADD-Like Apoptosis Regulating ProteinCFLAR protein, humanCflar protein, mouseIntracellular Signaling Peptides and ProteinsNeoplasm Proteins

Identifiers

PMID12885274
PMCPMC2984612
OpenAlexW2074584594

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.