Evidence map›Paper›PMID 11840265›Full record

ArticleLeukemia2002

TRAIL (Apo2L) suppresses growth of primary human leukemia and myelodysplasia progenitors.

M Plasilova, J Zivny, J Jelinek, R Neuwirtova, J Cermak, E Necas, L Andera, T Stopka

Open access · bronzeAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Leukemia, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Regulation of Tumor Necrosis Factor-related Apoptosis-inducing Ligand Expression in Primary Acute Leukemic Cells by Chemotherapeutics.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2013
    Article
  10. Proteasomal regulation of caspase-8 in cancer cell apoptosis.Apoptosis : an international journal on programmed cell death · 2013
    Article
  11. Article
  12. Establishment of reproducible xenotransplantation model of T cell acute lymphoblastic leukemia in NOD/SCID mice.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2012
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The promise of TRAIL--potential and risks of a novel anticancer therapy.Journal of molecular medicine (Berlin, Germany) · 2007
    Review
  18. Article
  19. Review
  20. 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

8 authors at 4 institutions in 1 country.

M PlasilovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
J Zivny
J Jelinek
R Neuwirtova
J Cermak
E Necas
L Andera
T Stopka
Institute of Haematology and Blood Transfusion · CZCharles University · CZCzech Academy of Sciences, Institute of Molecular Genetics · CZGeneral University Hospital in Prague · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL, APO2L) has been shown to induce apoptosis in a number of tumor cell lines as well as in some primary tumors whereas cells from most normal tissues are highly resistant to TRAIL-induced apoptosis. We have studied the susceptibility of primary malignant and normal bone marrow hematopoietic progenitors to TRAIL-induced apoptosis. Extracellular domain of human TRAIL with N-terminal His(6) tag (His-TRAIL, amino acids 95-281) was produced in E. coli and its apoptosis-inducing ability was compared with the leucine-zipper containing TRAIL, LZ-TRAIL. Both variants of TRAIL had the same apoptosis-inducing ability. Clonogenic progenitor assays showed that His-TRAIL significantly reduced the number of myeloid colonies (CFU-GM) and clusters from patients with acute myeloid leukemia (AML), chronic myeloid leukemia (CML), and myelodysplastic syndromes (MDS). His-TRAIL had no negative effect on the number of CFU-GM colonies and clusters derived from bone marrow cells of AML patients in complete remission, and lymphoma patients without bone marrow involvement, as well as those derived from normal cord blood cells. Moreover, we found that normal human stem cells treated with high doses of His-TRAIL maintain a repopulating potential when transplanted into NOD/SCID mice. To conclude, our data document that TRAIL does not affect normal human hematopoiesis but suppresses the growth of early primary leukemia and myelodysplasia progenitors.

Indexed as

Acute DiseaseAnimalsAntineoplastic AgentsApoptosisCell DifferentiationCells, CulturedColony-Forming Units AssayDrug Screening Assays, AntitumorGraft SurvivalGrowth InhibitorsHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHL-60 CellsHumansJurkat CellsK562 CellsAntineoplastic AgentsGrowth InhibitorsHis-TRAIL protein, recombinantLZ-TRAIL protein, recombinantMembrane GlycoproteinsPeptide FragmentsRecombinant Fusion ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID11840265
OpenAlexW2312277831

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.