Evidence map›Paper›PMID 20676135›Full record

ArticleOncogene2010

Phosphorylated p68 RNA helicase activates Snail1 transcription by promoting HDAC1 dissociation from the Snail1 promoter.

C L Carter, C Lin, C-Y Liu, L Yang, Z-R Liu

Abstract read
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Role of DEAD/DEAH-box helicases in immunity, infection and cancers.Cell communication and signaling : CCS · 2025
    Review
  3. Article
  4. Review
  5. The Role of Histone Deacetylases in Acute Lung Injury-Friend or Foe.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. RNA Helicases as Shadow Modulators of Cell Cycle Progression.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. P68 RNA helicase as a molecular target for cancer therapy.Journal of experimental & clinical cancer research : CR · 2014
    Review
  16. Review
  17. Article
  18. Review
  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

5 authors at 1 institution in 1 country.

C L CarterDepartment of Biology, Georgia State University, Atlanta, GA 30303, USA.
C Lin
C-Y Liu
L Yang
Z-R Liu
Georgia State University · US

Funding

P68 and Ca-calmodulin interaction in cell migrationR01CA118113 · NCI · GEORGIA STATE UNIVERSITY · PI LIU, ZHI-REN · 2007 to 2018
$2.3M
Biochemical Characterization of p68 RNA HelicaseR01GM063874 · NIGMS · GEORGIA STATE UNIVERSITY · PI LIU, ZHI-REN · 2003 to 2007
$1.1M
NCI NIH HHS CA118113NCI NIH HHS R01 CA118113NIGMS NIH HHS GM063874NIGMS NIH HHS R01 GM063874
6 · The paper itself

Abstract

The nuclear p68 RNA helicase is a prototypical member of the DEAD-box family of RNA helicases. p68 RNA helicase has been implicated in cell proliferation and early organ development and maturation. However, the functional role of p68 RNA helicase in these biological processes at the molecular level is not well understood. We previously reported that tyrosine phosphorylation of p68 RNA helicase mediates the effects of platelet-derived growth factor (PDGF) in induction of epithelial mesenchymal transition by promoting β-catenin nuclear translocation. Here, we report that phosphorylation of p68 RNA helicase at Y593 upregulates transcription of the Snail1 gene. The phosphorylated p68 activates transcription of the Snail1 gene by promoting histone deacetylase (HDAC)1 dissociation from the Snail1 promoter. Our results showed that p68 interacted with the nuclear remodeling and deacetylation complex MBD3:Mi-2/NuRD. Thus, our data suggested that a DEAD-box RNA unwindase could potentially regulate gene expression by functioning as a protein 'displacer' to modulate protein-protein interactions at the chromatin-remodeling complex.

Indexed as

Promoter Regions, Geneticbeta CateninCell DifferentiationCell NucleusCell ProliferationDEAD-box RNA HelicasesHistone Deacetylase 1HumansPhosphorylationPlatelet-Derived Growth FactorRegulatory Sequences, Nucleic AcidRNASnail Family Transcription FactorsTranscription FactorsUp-Regulationbeta CateninDEAD-box RNA HelicasesHDAC1 protein, humanHistone Deacetylase 1Platelet-Derived Growth FactorRNASNAI1 protein, humanSnail Family Transcription FactorsTranscription Factors

Identifiers

PMID20676135
PMCPMC2948064
OpenAlexW1985589749

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.