Evidence map›Paper›PMID 22627767›Full record

ArticleBlood2012

Sox4 cooperates with CREB in myeloid transformation.

Salemiz Sandoval, Christina Kraus, Er-Chieh Cho, Michelle Cho, Juraj Bies, Elena Manara, Benedetta Accordi, Elliot M Landaw, Linda Wolff, Martina Pigazzi and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2012. 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
3.3field-weighted citation impact, top 7% 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, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Zebrafish: a convenient tool for myelopoiesis research.Cell regeneration (London, England) · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. SOX4: The unappreciated oncogene.Seminars in cancer biology · 2020
    Review
  11. An integrated global regulatory network of hematopoietic precursor cell self-renewal and differentiation.Integrative biology : quantitative biosciences from nano to macro · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

11 authors at 7 institutions in 2 countries.

Salemiz SandovalDepartment of Pediatrics and Pathology & Laboratory Medicine, Gwynne Hazen, Cherry Memorial Laboratories, Mattel Children's Hospital, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Christina Kraus
Er-Chieh Cho
Michelle Cho
Juraj Bies
Elena Manara
Benedetta Accordi
Elliot M Landaw
Linda Wolff
Martina Pigazzi
Kathleen M Sakamoto
University of Padua · ITMattel Children's Hospital · USUniversity of California, Los Angeles · USLucile Packard Children's Hospital · USNational Cancer Institute · USNational Institutes of Health · USStanford University · US

Funding

The Role of CREB in Normal Myelopoiesis and LeukemogenesisR01HL075826 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAKAMOTO, KATHLEEN M · 2004 to 2013
$3.2M
Molecular and Cellular Characterization of Myeloproliferative DiseaseR01HL083077 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAKAMOTO, KATHLEEN M · 2005 to 2010
$1.5M
NHLBI NIH HHS R01 HL075826NHLBI NIH HHS R01 HL083077NHLBI NIH HHS R01 HL75826NHLBI NIH HHS R01 HL83077
6 · The paper itself

Abstract

The cAMP response element-binding protein (CREB) is a nuclear transcription factor that is critical for normal and neoplastic hematopoiesis. Previous studies have demonstrated that CREB is a proto-oncogene whose overexpression promotes cellular proliferation in hematopoietic cells. Transgenic mice that overexpress CREB in myeloid cells develop a myeloproliferative disease with splenomegaly and aberrant myelopoiesis. However, CREB overexpressing mice do not spontaneously develop acute myeloid leukemia. In this study, we used retroviral insertional mutagenesis to identify genes that accelerate leukemia in CREB transgenic mice. Our mutagenesis screen identified several integration sites, including oncogenes Gfi1, Myb, and Ras. The Sox4 transcription factor was identified by our screen as a gene that cooperates with CREB in myeloid leukemogenesis. We show that the transduction of CREB transgenic mouse bone marrow cells with a Sox4 retrovirus increases survival and self-renewal of cells in vitro. Furthermore, leukemic blasts from the majority of acute myeloid leukemia patients have higher CREB, phosphorylated CREB, and Sox 4 protein expression. Sox4 transduction of mouse bone marrow cells results in increased expression of CREB target genes. We also demonstrate that CREB is a direct target of Sox4 by chromatin immunoprecipitation assays. These results indicate that Sox4 and CREB cooperate and contribute to increased proliferation of hematopoietic progenitor cells.

Indexed as

AnimalsBone Marrow CellsCell ProliferationCell Transformation, NeoplasticCyclic AMP Response Element-Binding ProteinFemaleHL-60 CellsHumansK562 CellsLeukemia, Myeloid, AcuteMiceMice, Inbred C57BLMice, TransgenicMyeloid CellsPhosphorylationPregnancyCREB1 protein, humanCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinMAS1 protein, humanProto-Oncogene MasSOX4 protein, humanSox4 protein, mouseSOXC Transcription Factors

Identifiers

PMID22627767
PMCPMC3390953
OpenAlexW2046482386

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.