Evidence map›Paper›PMID 17473062›Full record

Trial reportBlood2007

Pivotal contributions of megakaryocytes to the biology of idiopathic myelofibrosis.

Stefan O Ciurea, Delwin Merchant, Nadim Mahmud, Takefumi Ishii, Yan Zhao, Wenyang Hu, Edward Bruno, Giovanni Barosi, Mingjiang Xu, Ronald Hoffman

Registry-linked trialOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04103645 (A 2-tiered, Phase 2, Rule-based, Intra-patient Dose Escalation Study to Investigate Safety and Feasibility of Vactosertib), which is not on this map. Cited by 122 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 6% 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.

NCT04103645 phase2terminatednot on this mapstarted 2019, after this paper: background citation

A 2-tiered, Phase 2, Rule-based, Intra-patient Dose Escalation Study to Investigate Safety and Feasibility of Vactosertib (TEW-7197) in the Treatment of Anemic Patients With Philadelphia Chromosome-negative MPNs (Ph-neg MPNs)

TypeinterventionalSponsorWeill Medical College of Cornell UniversityRan2019 to 2024Enrolled2ConditionsMyeloproliferative NeoplasmArmsVactosertib
3 · Its place in the literature

Who cites it

122 citing papers in PubMed, 1 synthesis or guideline pooled it, 210 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  9. Review
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  12. Review
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  19. Article
  20. Hematopoietic stem cells and extramedullary hematopoiesis in the lungs.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2023
    Review

62 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Stefan O CiureaHematology/Oncology Section, Department of Medicine, College of Medicine, University of Illinois at Chicago, IL, USA.
Delwin Merchant
Nadim Mahmud
Takefumi Ishii
Yan Zhao
Wenyang Hu
Edward Bruno
Giovanni Barosi
Mingjiang Xu
Ronald Hoffman
Illinois College · USUniversity of Illinois Chicago · USIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

Tissue BankP01CA108671 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ronald Hoffman · 2006 to 2026
$82.0M
NCI NIH HHS 1P01 CA 108671NCI NIH HHS P01 CA108671
6 · The paper itself

Abstract

In order to investigate the biologic processes underlying and resulting from the megakaryocytic hyperplasia that characterizes idiopathic myelofibrosis (IMF), peripheral blood CD34+ cells isolated from patients with IMF, polycythemia vera (PV), and G-CSF-mobilized healthy volunteers were cultured in the presence of stem cell factor and thrombopoietin. IMF CD34+ cells generated 24-fold greater numbers of megakaryocytes (MKs) than normal CD34+ cells. IMF MKs were also shown to have a delayed pattern of apoptosis and to overexpress the antiapoptotic protein bcl-xL. MK hyperplasia in IMF is, therefore, likely a consequence of both the increased ability of IMF progenitor cells to generate MKs and a decreased rate of MK apoptosis. Media conditioned (CM) by CD61+ cells generated in vitro from CD34+ cells were then assayed for the levels of growth factors and proteases. Higher levels of transforming growth factor-beta (TGF-beta) and active matrix metalloproteinase-9 (MMP9) were observed in media conditioned with IMF CD61+ cells than normal or PV CD61+ cells. Both normal and IMF CD61+ cells produced similar levels of VEGF. MK-derived TGF-B and MMP-9, therefore, likely contribute to the development of many pathological epiphenomena associated with IMF.

Indexed as

AdultAgedAntigens, CD34Apoptosisbcl-X ProteinCells, CulturedCulture Media, ConditionedFemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHumansHyperplasiaIntegrin beta3MaleMatrix Metalloproteinase 9Antigens, CD34BCL2L1 protein, humanbcl-X ProteinCulture Media, ConditionedGranulocyte Colony-Stimulating FactorIntegrin beta3ITGB3 protein, humanMatrix Metalloproteinase 9ThrombopoietinTransforming Growth Factor betaVascular Endothelial Growth Factor A

Identifiers

PMID17473062
PMCPMC1924766
OpenAlexW2052033797

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.