Evidence map›Paper›PMID 24613413›Full record

ArticleCancer cell2014

Clonal evolution enhances leukemia-propagating cell frequency in T cell acute lymphoblastic leukemia through Akt/mTORC1 pathway activation.

Jessica S Blackburn, Sali Liu, Jayme L Wilder, Kimberly P Dobrinski, Riadh Lobbardi, Finola E Moore, Sarah A Martinez, Eleanor Y Chen, Charles Lee, David M Langenau

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

68 citing papers in PubMed, 116 citations in OpenAlex.

  1. Review
  2. A novel regulatory circuit of ATG4B and SESN3 promotes T cell leukemogenesis.Journal of experimental & clinical cancer research : CR · 2025
    Article
  3. Article
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  7. Direct male development in chromosomally ZZ zebrafish.Frontiers in cell and developmental biology · 2024
    Article
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  10. Review
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  15. Zebrafish models of acute leukemias: Current models and future directions.Wiley interdisciplinary reviews. Developmental biology · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

8 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 6 institutions in 2 countries.

Jessica S BlackburnDepartment of Pathology, Regenerative Medicine and Center for Cancer Research, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Boston, MA 02138, USA.
Sali LiuNorthwestern University, Chicago, IL 60208, USA.
Jayme L WilderHarvard Stem Cell Institute, Boston, MA 02138, USA.
Kimberly P DobrinskiCenter for Integrative Medicine, University of South Florida, Tampa, FL 33620, USA.
Riadh LobbardiDepartment of Pathology, Regenerative Medicine and Center for Cancer Research, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Boston, MA 02138, USA.
Finola E MooreDepartment of Pathology, Regenerative Medicine and Center for Cancer Research, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Boston, MA 02138, USA.
Sarah A MartinezDepartment of Pathology, Regenerative Medicine and Center for Cancer Research, Massachusetts General Hospital, Boston, MA 02114, USA.
Eleanor Y ChenDepartment of Pathology, Regenerative Medicine and Center for Cancer Research, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Boston, MA 02138, USA; Department of Pathology, University of Washington Medical Center, Seattle, WA 98195, USA.
Charles LeeThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06030, USA; Department of Graduate Studies, Seoul National University School of Medicine, Seoul 110-744, South Korea.
David M LangenauDepartment of Pathology, Regenerative Medicine and Center for Cancer Research, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Stem Cell Institute, Boston, MA 02138, USA. Electronic address: dlangenau@mgh.harvard.edu.
Massachusetts General Hospital · USHarvard Stem Cell Institute · USCenter for Cancer Research · USJackson Laboratory · USNorthwestern University · USUniversity of South Florida · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Jeffrey Hsu-Min Chuang · 1985 to 2026
$61.9M
MOLECULAR IMMUNOLOGY AND TUMOR BIOLOGYT32CA009216 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI David Michael Langenau · 1985 to 2026
$10.6M
The role of the protein tyrosine phosphatase PRL3 in leukemia developmentK99CA181500 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BLACKBURN, JESSICA S. · 2014 to 2015
$346k
The Role of Phf6 in HematopoiesisF32DK098875 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, FINOLA ELIZABETH · 2013 to 2015
$165k
NCI NIH HHS K99 CA181500NCI NIH HHS P30 CA034196NCI NIH HHS T32 CA009216NIDDK NIH HHS F32 DK098875
6 · The paper itself

Abstract

Clonal evolution and intratumoral heterogeneity drive cancer progression through unknown molecular mechanisms. To address this issue, functional differences between single T cell acute lymphoblastic leukemia (T-ALL) clones were assessed using a zebrafish transgenic model. Functional variation was observed within individual clones, with a minority of clones enhancing growth rate and leukemia-propagating potential with time. Akt pathway activation was acquired in a subset of these evolved clones, which increased the number of leukemia-propagating cells through activating mTORC1, elevated growth rate likely by stabilizing the Myc protein, and rendered cells resistant to dexamethasone, which was reversed by combined treatment with an Akt inhibitor. Thus, T-ALL clones spontaneously and continuously evolve to drive leukemia progression even in the absence of therapy-induced selection.

Indexed as

AnimalsAnimals, Genetically ModifiedAntineoplastic Agents, HormonalApoptosisCell Line, TumorCell ProliferationCell Transformation, NeoplasticClonal EvolutionDexamethasoneDisease ProgressionDrug Resistance, NeoplasmEnzyme ActivationGenetic VariationHeterocyclic Compounds, 3-RingHumansMechanistic Target of Rapamycin Complex 1Antineoplastic Agents, HormonalDexamethasoneHeterocyclic Compounds, 3-RingMechanistic Target of Rapamycin Complex 1MK 2206Multiprotein ComplexesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mycTOR Serine-Threonine Kinases

Identifiers

PMID24613413
PMCPMC3992437
OpenAlexW2144051719

What OpenQuestion holds

Textmetadata
LicenceTDM
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.