Evidence map›Paper›PMID 22830400›Full record

ReviewFuture oncology (London, England)2012

Large granular lymphocyte leukemia: from dysregulated pathways to therapeutic targets.

Francis Leblanc, Dan Zhang, Xin Liu, Thomas P Loughran

Open access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. The role of interferons type I, II and III in myositis: A review.Brain pathology (Zurich, Switzerland) · 2021
    Review
  12. Article
  13. Identification of aHaematologica · 2020
    Article
  14. Review
  15. Genomics of LGL leukemia and select other rare leukemia/lymphomas.Best practice & research. Clinical haematology · 2019
    Review
  16. Article
  17. Oncotarget · 2017
    Article
  18. Review
  19. Article
  20. Article
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 at 1 institution in 1 country.

Francis LeblancPenn State Hershey Cancer Institute, Experimental Therapeutics, Room 4427, 500 University Drive, PO Box 850, Hershey, PA 17033-0850, USA.
Dan Zhang
Xin Liu
Thomas P Loughran
Penn State Milton S. Hershey Medical Center · US

Funding

Survival Mechanisms in Leukemic NK CellsR01CA098472 · NCI · UNIVERSITY OF VIRGINIA · PI LOUGHRAN, THOMAS P. · 2003 to 2016
$4.0M
Targeted Therapeutics of LGL Leukemia utilizing Ceramide NanoliposomesR01CA133525 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI LOUGHRAN, THOMAS P. · 2008 to 2012
$1.6M
NCI NIH HHS R01 CA098472NCI NIH HHS R01 CA133525
6 · The paper itself

Abstract

Large granular lymphocyte (LGL) leukemia is a clonal lymphoproliferative disorder of cytotoxic lymphocytes characterized by an expansion of CD3(+) cytotoxic T lymphocytes or CD3(-) natural killer cells. Patients present with various cytopenias including neutropenia, anemia and thrombocytopenia. In addition, there is an association of T-cell large granular lymphocytic leukemia with rheumatoid arthritis. It is believed that LGL leukemia begins as an antigen-driven immune response with subsequent constitutive activation of cytotoxic T lymphocytes or natural killer cells through PDGF and IL-15 contributing to their survival. Consequently, this leads to a dysregulation of apoptosis and dysfunction of the activation-induced cell death pathway. Treatment of LGL leukemia is based on a low-dose immunosuppressive regimen using methotrexate or cyclophosphamide. However, no standard of therapy has been established, as large prospective trials have not been conducted. In addition, some patients are refractory to treatment. The lack of a curative therapy for LGL leukemia means that new treatment options are needed. Insight into the various dysregulated signaling pathways in LGL leukemia may provide novel therapeutic treatment modalities.

Indexed as

ApoptosisCyclophosphamideFas Ligand ProteinHumansImmunosuppressive AgentsInterleukin-15Killer Cells, NaturalLeukemia, Large Granular LymphocyticMethotrexateNF-kappa BProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-rafras ProteinsSignal TransductionSphingolipidsT-Lymphocytes, CytotoxicCyclophosphamideFas Ligand ProteinImmunosuppressive AgentsInterleukin-15MethotrexateNF-kappa BProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-rafras ProteinsSphingolipids

Identifiers

PMID22830400
PMCPMC3464048
OpenAlexW2001249568

What OpenQuestion holds

Textmetadata
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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.