Evidence map›Paper›PMID 18794800›Full record

ArticleOncogene2008

RAN GTPase is an effector of the invasive/metastatic phenotype induced by osteopontin.

V V Kurisetty, P G Johnston, N Johnston, P Erwin, P Crowe, D G Fernig, F C Campbell, I P Anderson, P S Rudland, M K El-Tanani

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 10% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Ran GTPase and Its Importance in Cellular Signaling and Malignant Phenotype.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Nanoparticulate RNA delivery systems in cancer.Cancer reports (Hoboken, N.J.) · 2020
    Review
  13. Article
  14. Ran GTPase: A Key Player in Tumor Progression and Metastasis.Frontiers in cell and developmental biology · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Identification and Expression Profiling of theInternational journal of molecular sciences · 2019
    Article
  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

10 authors at 3 institutions in 2 countries.

V V KurisettyCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, UK.
P G Johnston
N Johnston
P Erwin
P Crowe
D G Fernig
F C Campbell
I P Anderson
P S Rudland
M K El-Tanani
Queen's University Belfast · GBCancer and Polio Research Fund · GBCentre for Cancer Biology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteopontin (OPN) is a phosphorylated glycoprotein that binds to alpha v-containing integrins and is important in malignant transformation and cancer. Previously, we have utilized suppressive subtractive hybridization between mRNAs isolated from the Rama 37 (R37) rat mammary cell line and a subclone rendered invasive and metastatic by stable transfection with an expression vector for OPN to identify RAN GTPase (RAN) as the most overexpressed gene, in addition to that of OPN. Here we show that transfection of noninvasive R37 cells with an expression vector for RAN resulted in increased anchorage-independent growth, cell attachment and invasion through Matrigel in vitro, and metastasis in syngeneic rats. This induction of a malignant phenotype was induced independently of the expression of OPN, and was reversed by specifically reducing the expression of RAN using small-interfering RNAs. By using a combination of mutant protein and inhibitors, it was found that RAN signal transduction occurred through the c-Met receptor and PI3 kinase. This study therefore identifies RAN as a novel effector of OPN-mediated malignant transformation and some of its downstream signaling events in a mammary epithelial model of cancer invasion/metastasis.

Indexed as

AnimalsBlotting, NorthernBlotting, WesternCell Line, TumorCell ProliferationCell Transformation, NeoplasticFemaleFluorescent Antibody TechniqueGene ExpressionImmunohistochemistryMammary Neoplasms, ExperimentalNeoplasm InvasivenessOsteopontinPhenotypePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-metOsteopontinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-metran GTP-Binding ProteinRNA, Small Interfering

Identifiers

PMID18794800
OpenAlexW2033655686

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.