Evidence map›Paper›PMID 10851064›Full record

ReviewOncogene2000

Pharmaceutical intervention in the JAK/STAT signaling pathway.

H M Seidel, P Lamb, J Rosen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Pancreatic Cancer: Beyond Brca Mutations.Journal of personalized medicine · 2022
    Review
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  10. Review
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  13. Onco-nephrology: an appraisal of the cancer and chronic kidney disease links.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2015
    Review
  14. Article
  15. 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

3 authors at 1 institution in 1 country.

H M SeidelLigand Pharmaceuticals, 10275 Science Center Drive, San Diego, California, CA 92121, USA.
P Lamb
J Rosen
Ligand Pharmaceuticals (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many cytokines exert their effect via the JAK/STAT signal transduction pathway. Due to the medical relevance of many of these cytokines, they are being exploited, either directly, or through antagonists, as therapeutics for a variety of serious diseases. Currently, these therapeutics consist almost entirely of protein products, with all of their attendant drawbacks. Delineation of the signaling mechanisms for the cytokines, however, has allowed the design and implementation of a variety of cell-based and biochemical screens for small molecule mimics or antagonists of these cytokines. Several successful assays will be described along with the advantages of each type of assay. Use of assays of this type should make it possible to discover numerous small molecule cytokine modulators with significant utility in the clinic. Oncogene (2000).

Indexed as

Drug Evaluation, PreclinicalSignal TransductionAnimalsCell LineCytokinesDNA-Binding ProteinsEnzyme ActivationEnzyme InhibitorsGrowth SubstancesHumansJanus Kinase 1Molecular MimicryProtein BindingProtein-Tyrosine KinasesSTAT1 Transcription FactorTrans-ActivatorsCytokinesDNA-Binding ProteinsEnzyme InhibitorsGrowth SubstancesJAK1 protein, humanJanus Kinase 1Protein-Tyrosine KinasesSTAT1 protein, humanSTAT1 Transcription FactorTrans-Activators

Identifiers

PMID10851064
OpenAlexW2322090980

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.