Evidence map›Paper›PMID 14701873›Full record

ArticleGenes & development2003

Similar MLL-associated leukemias arising from self-renewing stem cells and short-lived myeloid progenitors.

Antonio Cozzio, Emmanuelle Passegué, Paul M Ayton, Holger Karsunky, Michael L Cleary, Irving L Weissman

Abstract read
In one paragraph

Article in Genes & development, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 291 papers.

0numbers the graph read from it
0cells of the map it votes in
291citing papers in PubMed
–field-weighted citation impact
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

291 citing papers in PubMed.

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  10. Targeting the N-cadherin/Frontiers in oncology · 2025
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231 more citing papers are in PubMed but not listed here.

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

6 authors.

Antonio CozzioDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Emmanuelle Passegué
Paul M Ayton
Holger Karsunky
Michael L Cleary
Irving L Weissman

Funding

MOLECULAR CHARACTERIZATION OF ACUTE MYELOID LEUKEMIAR01CA086017 · NCI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2000 to 2015
$5.5M
NCI NIH HHS CA 55209NCI NIH HHS CA 86017NCI NIH HHS R01 CA086017
6 · The paper itself

Abstract

We have used the hematopoietic system as a model to investigate whether acute myeloid leukemia arises exclusively from self-renewing stem cells or also from short-lived myeloid progenitors. When transduced with a leukemogenic MLL fusion gene, prospectively isolated stem cells and myeloid progenitor populations with granulocyte/macrophage differentiation potential are efficiently immortalized in vitro and result in the rapid onset of acute myeloid leukemia with similar latencies following transplantation in vivo. Regardless of initiating cell, leukemias displayed immunophenotypes and gene expression profiles characteristic of maturation arrest at an identical late stage of myelomonocytic differentiation, putatively a monopotent monocytic progenitor stage. Our findings unequivocally establish the ability of transient repopulating progenitors to initiate myeloid leukemias in response to an MLL oncogene, and support the existence of cancer stem cells that do not necessarily overlap with multipotent stem cells of the tissue of origin.

Indexed as

Acute DiseaseAnimalsCell DifferentiationCell LineageCell Transformation, NeoplasticGene Expression Regulation, DevelopmentalGenetic VectorsGene Transfer TechniquesGranulocytesHematopoietic Stem CellsHumansImmunophenotypingLeukemia, MyeloidMacrophagesMiceMice, Inbred C57BLMLL-ENL oncoprotein, humanMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, Fusion

Identifiers

PMID14701873
PMCPMC305255

What OpenQuestion holds

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Registered trials

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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.