Evidence map›Paper›PMID 17103319›Full record

ArticleJournal of bioenergetics and biomembranes2006

H-prune-nm23-H1 protein complex and correlation to pathways in cancer metastasis.

Livia Garzia, Cristin Roma, Nicoletta Tata, Daniela Pagnozzi, Piero Pucci, Massimo Zollo

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of bioenergetics and biomembranes, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Oncogenic Epstein-Barr virus recruits Nm23-H1 to regulate chromatin modifiers.Laboratory investigation; a journal of technical methods and pathology · 2018
    Review
  8. Article
  9. Review
  10. Regulation of the metastasis suppressor Nm23-H1 by tumor viruses.Naunyn-Schmiedeberg's archives of pharmacology · 2015
    Review
  11. Recruited metastasis suppressor NM23-H2 attenuates expression and activity of peroxisome proliferator-activated receptor δ (PPARδ) in human cholangiocarcinoma.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2015
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. The NM23 family in development.Molecular and cellular biochemistry · 2009
    Review
  17. Article
  18. Article
  19. Understanding h-prune biology in the fight against cancer.Clinical & experimental metastasis · 2007
    Review
  20. PRUNE and NM23-M1 expression in embryonic and adult mouse brain.Journal of bioenergetics and biomembranes · 2006
    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 1 institution in 1 country.

Livia GarziaCentro di Ingegneria Genetica e Biotecnologia Avanzate, CEINGE, Via Comunale Margherita 482, 80131, Naples, Italy.
Cristin Roma
Nicoletta Tata
Daniela Pagnozzi
Piero Pucci
Massimo Zollo
Tecnologie Avanzate (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a multi-step process, one of the latest events correspond to metastasis formation and dissemination, to date the major cause of deaths. The h-prune-nm23-H1 protein complex and its activation of PDE-cAMP activity have been shown to correlate with breast cancer progression and metastasis formation. Here, we describe the protein complex formation and its involvement in cell migration. By gene expression studies and protein-protein pull-down analyses coupled to mass spectrometry we have identified new genes and pathways along which the h-prune-nm23-H1 complex exerts its function. We review here h-prune binding to the glycogen synthase kinase (GSK-3beta) and identify a new h-prune protein partner, Gelsolin, an ATP severing protein acting in focal adhesions, in a MDA-435 breast cancer cellular model. The results presented here underline the importance of this protein complex leading to new translational studies involved into the inhibition of cell migration, thus enhancing the potential of using this knowledge to direct inhibition of metastases formation in humans.

Indexed as

Breast NeoplasmsCarrier ProteinsCell Line, TumorCell MovementGelsolinGene Expression Regulation, NeoplasticGlycogen Synthase Kinase 3HumansImmunoprecipitationMass SpectrometryMultiprotein ComplexesNeoplasm MetastasisNM23 Nucleoside Diphosphate KinasesNucleoside-Diphosphate KinasePhosphoric Monoester HydrolasesSignal TransductionCarrier ProteinsGelsolinGlycogen Synthase Kinase 3Multiprotein ComplexesNM23 Nucleoside Diphosphate KinasesNME1 protein, humanNucleoside-Diphosphate KinasePhosphoric Monoester HydrolasesPRUNE1 protein, human

Identifiers

PMID17103319
OpenAlexW1988350216

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.