Evidence map›Paper›PMID 24183236›Full record

ArticleLeukemia research2014

G0S2 inhibits the proliferation of K562 cells by interacting with nucleolin in the cytosol.

Takeshi Yamada, Chun Shik Park, Ye Shen, Karen R Rabin, H Daniel Lacorazza

Open access · greenAbstract read
In one paragraph

Article in Leukemia research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Lipolytic inhibitor G0S2 modulates glioma stem-like cell radiation response.Journal of experimental & clinical cancer research : CR · 2019
    Article
  11. Article
  12. Article
  13. Oncotarget · 2018
    Article
  14. Adipose Triglyceride Lipase Regulation: An Overview.Current protein & peptide science · 2018
    Review
  15. G0S2: A small giant controller of lipolysis and adipose-liver fatty acid flux.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2017
    Review
  16. Article
  17. Article
  18. G0/G1 Switch Gene 2 Regulates Cardiac Lipolysis.The Journal of biological chemistry · 2015
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Takeshi YamadaDepartment of Pathology & Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA.
Chun Shik ParkDepartment of Pathology & Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA.
Ye ShenDepartment of Pathology & Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA.
Karen R RabinDepartment of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA.
H Daniel LacorazzaDepartment of Pathology & Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA. Electronic address: hdl@bcm.edu.
Texas Children's Hospital · USBaylor College of Medicine · US

Funding

Transcriptional Regulation of Development and Maintenance of Memory T LymphocytesR01AI077536 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI LACORAZZA, DANIEL · 2008 to 2011
$1.7M
NIAID NIH HHS R01 AI077536NIAID NIH HHS R01-AI077536NIAID NIH HHS R01-AI077536-02S1
6 · The paper itself

Abstract

G0/G1 switch gene 2 (G0S2) is a basic protein with ill-defined function that inhibits the proliferation of hematopoietic stem cells. Herein, we show that treatment of K562 cells with 5-azacytidine (5-Aza) resulted in a 24-fold increase in G0S2 expression and a reduction in cell growth. Conversely, gene demethylation in the presence of G0S2-specific shRNA restored proliferation, further supporting an inhibitory role for G0S2 in cell proliferation. Elevated levels of G0S2 inhibited the division of K562 cells by sequestering the nucleolar phosphoprotein nucleolin in the cytosol. G0S2 inhibited the proliferation of leukemia cells in vivo in xenograft models. Collectively, our data identify a new mechanism that controls proliferation in K562 cells, suggesting a possible tumor suppressor function in leukemia cells.

Indexed as

Cell ProliferationAnimalsCell Cycle ProteinsCells, CulturedCytosolGenes, Tumor SuppressorHL-60 CellsHumansK562 CellsMiceMice, NudeNucleolinPhosphoproteinsProtein BindingRNA-Binding ProteinsRNA, Small InterferingCell Cycle ProteinsG0S2 protein, humanNucleolinPhosphoproteinsRNA-Binding ProteinsRNA, Small InterferingG0S2K562NucleolinProliferation

Identifiers

PMID24183236
PMCPMC3946941
OpenAlexW2146586666

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.