Evidence map›Paper›PMID 24705981›Full record

ReviewThe oncologist2014

STAT3 inhibitors: finding a home in lymphoma and leukemia.

Javier Munoz, Navjot Dhillon, Filip Janku, Stephanie S Watowich, David S Hong

Open access · bronzeAbstract readReview
In one paragraph

Review in The oncologist, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. B cell-Derived IL35 Drives STAT3-Dependent CD8Cancer immunology research · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. The role of the JAK/STAT signal pathway in rheumatoid arthritis.Therapeutic advances in musculoskeletal disease · 2018
    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

5 authors at 3 institutions in 1 country.

Javier MunozHematology-Oncology, Banner, MD Anderson Cancer Center, Gilbert, Arizona, USA; Hematology-Oncology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA; Departments of Investigational Cancer Therapeutics (Phase I Clinical Trials Program) and Immunology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Navjot Dhillon
Filip Janku
Stephanie S Watowich
David S Hong
The University of Texas MD Anderson Cancer Center · USBanner MD Anderson Cancer CenterLouisiana State University Health Sciences Center New Orleans · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The Janus kinase (JAK) and signal transducer and activator of transcription (STAT) pathway is an active mediator of cytokine signaling in the pathogenesis of solid and hematologic malignancies. The seven-member STAT family is composed of latent cytoplasmic transcription factors that are activated by phosphorylation intertwined in a network with activation that ultimately leads to cell proliferation. An activated kinase enzyme phosphorylates one STAT factor or more, which shuttle to the nucleus to regulate gene expression, promoting cell survival. Somatic STAT3 mutations have been recently reported in large granular lymphocytic leukemia, aplastic anemia, and myelodysplastic syndrome. Furthermore, the relationship between BCL6 and STAT3 in diffuse large B-cell lymphomas, particularly on the activated B-cell subtype, needs to be further explored. The search for therapeutic STAT3 inhibitors that abrogate the JAK/STAT pathway is currently under way. Targeting the STAT pathway, which seems to be critical in tumorigenesis, is promising for multiple malignancies including lymphoma and leukemia. In this paper, we review mechanisms of action, failures, and successes of STAT3 inhibitors.

Indexed as

Cell ProliferationCell SurvivalDNA-Binding ProteinsGene Expression Regulation, NeoplasticHumansInterleukin-6Interleukin-6 InhibitorsJanus KinasesLeukemiaLymphomaPhosphorylationProto-Oncogene Proteins c-bcl-6STAT3 Transcription FactorBCL6 protein, humanDNA-Binding ProteinsIL6 protein, humanInterleukin-6Interleukin-6 InhibitorsJanus KinasesProto-Oncogene Proteins c-bcl-6STAT3 protein, humanSTAT3 Transcription FactorIL6JAKLeukemiaLymphomaPhase ISTAT

Identifiers

PMID24705981
PMCPMC4012967
OpenAlexW2111237323

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.