Evidence map›Paper›PMID 16204320›Full record

ArticleBlood2006

Sox4 cooperates with Evi1 in AKXD-23 myeloid tumors via transactivation of proviral LTR.

Kathryn E Boyd, Ying-Yi Xiao, Kai Fan, Amanda Poholek, Neal G Copeland, Nancy A Jenkins, Archibald S Perkins

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

32 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Zebrafish: a convenient tool for myelopoiesis research.Cell regeneration (London, England) · 2023
    Review
  5. SOX4: The unappreciated oncogene.Seminars in cancer biology · 2020
    Review
  6. Article
  7. Article
  8. Article
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  10. Article
  11. Article
  12. Article
  13. Review
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  15. Article
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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

7 authors at 2 institutions in 1 country.

Kathryn E BoydMouse Cancer Genetics Program, National Cancer Institute, Frederick, MD, USA.
Ying-Yi Xiao
Kai Fan
Amanda Poholek
Neal G Copeland
Nancy A Jenkins
Archibald S Perkins
Yale University · USHouston Methodist · US

Funding

DEREGULATION OF MYELOPOIESIS BY ZINC FINGER PROTEIN EVI1R01CA081216 · NCI · YALE UNIVERSITY · PI PERKINS, ARCHIBALD S · 1999 to 2004
$962k
STUDY OF A PUTATIVE TUMOR SUPPRESSOR GENE IN LEUKEMIAF32CA088467 · NCI · YALE UNIVERSITY · PI BOYD, KATHRYN E · 2000 to 2002
$95k
NCI NIH HHS 1F32CA88467-01NCI NIH HHS R01 CA81216
6 · The paper itself

Abstract

Myeloid leukemias in AKXD23 mice contain proviral insertions at Evi1, resulting in transcriptional activation. Although Evi1 is clearly involved in leukemia, gene transfer studies in mice with Evi1 fail to cause leukemia, arguing that cooperating events are necessary. We reanalyzed AKXD-23 tumors for cooperating proviral insertion and found that each tumor had a proviral insertion in Sox4, which encodes an HMG-box transcription factor. RNA analysis revealed these insertions cause increased Sox4 expression. Overexpression of Sox4 in 32Dcl3 cells markedly inhibited cytokine-induced granulocyte maturation, as documented by morphologic and mRNA analysis. Sox4-expressing cells had higher levels of transcripts associated with proliferation, including Evi1. Conversely, in leukemic cells that express Sox4 and bear provirally activated Evi1, suppression of Sox4 with short hairpin RNAs resulted in down-regulation of both Sox4 and Evi1. By cotransfection studies, Sox4 is able to transactivate the AKV long terminal repeat, which likely explains how Sox4 transcriptionally up-regulates provirally activated Evi1; however, Sox4 does not appear to regulate the native Evi1 promoter. We propose that Sox4 proviral activation is selected for in the setting of prior proviral activation of Evi1, because it transactivates the relatively weak LTR of AKV leading to higher Evi1 expression and consequent block to differentiation.

Indexed as

ProvirusesTerminal Repeat SequencesTranscriptional ActivationAnimalsBiomarkers, TumorCell DifferentiationCell ProliferationCytokinesDNA-Binding ProteinsDown-RegulationGene Expression ProfilingGranulocytesHigh Mobility Group ProteinsLeukemia, MyeloidMDS1 and EVI1 Complex Locus ProteinMiceBiomarkers, TumorCytokinesDNA-Binding ProteinsHigh Mobility Group ProteinsMDS1 and EVI1 Complex Locus ProteinMecom protein, mouseRNA, MessengerRNA, Small InterferingSox4 protein, mouseSOXC Transcription FactorsTrans-ActivatorsTranscription Factors

Identifiers

PMID16204320
PMCPMC1895620
OpenAlexW2001421157

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.