Evidence map›Paper›PMID 18579579›Full record

ArticleHuman molecular genetics2008

ATP modulates PTEN subcellular localization in multiple cancer cell lines.

Glenn P Lobo, Kristin A Waite, Sarah M Planchon, Todd Romigh, Janet A Houghton, Charis Eng

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. PTEN in Hereditary and Sporadic Cancer.Cold Spring Harbor perspectives in medicine · 2020
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Balancing Proliferation and Connectivity in PTEN-associated Autism Spectrum Disorder.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2015
    Review
  10. Article
  11. Article
  12. Purinergic signalling and cancer.Purinergic signalling · 2013
    Review
  13. Cytoplasmic PTEN protein loss distinguishes intraductal carcinoma of the prostate from high-grade prostatic intraepithelial neoplasia.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2013
    Article
  14. Article
  15. Article
  16. Article
  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

6 authors at 2 institutions in 1 country.

Glenn P LoboGenomic Medicine Institute, Cleveland Clinic Foundation, 9500 Euclid Ave, NE-50, Cleveland, OH 44195, USA.
Kristin A Waite
Sarah M Planchon
Todd Romigh
Janet A Houghton
Charis Eng
Cerner (United States) · USCleveland Clinic · US

Funding

PTEN Nuclear-Cytoplasmic Localization in Breast CancerR01CA118980 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI ENG, CHARIS · 2007 to 2011
$1.8M
NCI NIH HHS 1R01CA118980-01A2
6 · The paper itself

Abstract

The tumour suppressor gene PTEN plays an important somatic role in both hereditary and sporadic breast carcinogenesis. While the role of PTEN's lipid phosphatase activity, as a negative regulator of the cytoplasmic phosphatidylinositol-3-kinase/Akt pathway is well known, it is now well established that PTEN exists and functions in the nucleus. Multiple mechanisms of regulating PTEN's subcellular localization have been reported. However none are ubiquitous across multiple cancer cell lines and tissue types. We show here that adenosine triphosphate (ATP) regulates PTEN subcellular localization in a variety of different cancer cell lines, including those derived from breast, colon and thyroid carcinomas. Cells deficient in ATP show an increased level of nuclear PTEN protein. This increase in PTEN is reversed when cells are supplemented with ATP, ADP or AMP. In contrast, the addition of the non-hydrolyzable analogue ATPgammaS, did not reverse nuclear PTEN protein levels in all the cell types tested. To our knowledge, this is the first report that describes a regulation of PTEN subcellular localization that is not specific to one cell line or tissue type, but appears to be common across a variety of cell lineages.

Indexed as

Adenosine TriphosphateBreast NeoplasmsCell Line, TumorCell NucleusColorectal NeoplasmsHumansProtein TransportPTEN PhosphohydrolaseThyroid NeoplasmsAdenosine TriphosphatePTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID18579579
PMCPMC2525500
OpenAlexW2122738886

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.