Evidence map›Paper›PMID 22150312›Full record

ReviewCritical reviews in oncogenesis2011

The role of stem cell factor SALL4 in leukemogenesis.

Chong Gao, Nikki R Kong, Li Chai

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in oncogenesis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. SALL4 Oncogenic Function in Cancers: Mechanisms and Therapeutic Relevance.International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. SALL4 Gene Expression in Acute Myeloid Leukemia.Asian Pacific journal of cancer prevention : APJCP · 2019
    Article
  6. Review
  7. Targeting cancer addiction for SALL4 by shifting its transcriptome with a pharmacologic peptide.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  8. Article
  9. Review
  10. Article
  11. Anticancer Properties of Chrysin on Colon Cancer Cells,Iranian journal of biotechnology · 2016
    Article
  12. Epigenetic Regulation of Hematopoietic Stem Cells.International journal of stem cells · 2016
    Review
  13. Do short, frequent DNA sequence motifs mould the epigenome?Nature reviews. Molecular cell biology · 2016
    Review
  14. Article
  15. Inhibition of SALL4 suppresses carcinogenesis of colorectal cancer via regulating Gli1 expression.International journal of clinical and experimental pathology · 2015
    Article
  16. SALL4: engine of cell stemness.Current gene therapy · 2014
    Review
  17. Article
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Chong GaoDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Nikki R Kong
Li Chai
Brigham and Women's Hospital · US

Funding

Transcription regulation in hematopoiesisP01HL095489 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI PARK, SHINYOUNG · 2010 to 2020
$20.1M
Hematopoietic stem cell commitmentP01DK080665 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TENEN, DANIEL G · 2008 to 2012
$7.3M
SELF-RENEWAL IN LEUKEMIC STEM CELLSR01HL092437 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CHAI, LI · 2008 to 2012
$2.4M
NHLBI NIH HHS P01 HL095489NHLBI NIH HHS P01HL095489NHLBI NIH HHS R01 HL092437NHLBI NIH HHS R01HL092437NHLBI NIH HHS R01HL092437-A1S1NIDDK NIH HHS P01 DK080665NIDDK NIH HHS P01DK080665
6 · The paper itself

Abstract

SALL4, a member of the SALL gene family, is one of the most important transcriptional regulators of stem cells. It is of particular interest to stem cell biologists because it is linked to the self-renewal of both embryonic stem cells (ESCs) and hematopoietic stem cells (HSCs), and it is involved in human leukemia. In ESCs, the Sall4/Oct4/Nanog core transcriptional network governs the self-renewal and pluripotent properties of human and murine ESCs. In normal HSCs and leukemic stem cells (LSCs), SALL4 is linked to three known pathways that are involved in self-renewal: Wnt/β-catenin, Bmi-1, and Pten. Despite the important shared role of SALL4 in self-renewal of HSCs and LSCs, our recent studies obtained through correlating global downstream target genes and unique functional studies in normal versus leukemic cells have demonstrated that SALL4 has differential effects on both pro- and anti-apoptotic pathways in normal and leukemic cells. Targeting SALL4, particularly when combined with the use of ABT-737, a BCL2 antagonist, could lead to leukemic cell-specific apoptosis. This review summarizes our current knowledge on the SALL gene family development, particularly on the role of SALL4 in stem cells, as well as tumorigenesis, especially leukemogenesis.

Indexed as

Cell Transformation, NeoplasticAnimalsGene Expression Regulation, DevelopmentalHumansLeukemiaMiceTranscription FactorsSALL4 protein, humanTranscription Factors

Identifiers

PMID22150312
PMCPMC3238789
OpenAlexW1975773685

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.