Evidence map›Paper›PMID 23563176›Full record

ArticleOncogene2014

Tax-interacting protein 1 coordinates the spatiotemporal activation of Rho GTPases and regulates the infiltrative growth of human glioblastoma.

H Wang, M Han, W Whetsell, J Wang, J Rich, D Hallahan, Z Han

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Blocking the functional domain of TIP1 by antibodies sensitizes cancer to radiation therapy.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    Article
  6. Review
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  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. PLEKHG5 is a novel prognostic biomarker in glioma patients.International journal of clinical oncology · 2019
    Article
  15. PEGylated peptide to TIP1 is a novel targeting agent that binds specifically to various cancers in vivo.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Article
  16. Review
  17. Article
  18. Article
  19. Article
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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

7 authors at 3 institutions in 1 country.

H Wang1] Department of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, TN, USA [2] Department of Cancer Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.
M Han1] Department of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, TN, USA [2] Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Chinese Academy of Science, Kunming, China [3] Graduate School, Chinese Academy of Sciences, Beijing, China.
W WhetsellDepartment of Pathology, Vanderbilt University School of Medicine, Nashville, TN, USA.
J Wang1] Department of Neurological Surgery, Vanderbilt University School of Medicine, Nashville, TN, USA [2] Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN, USA.
J RichDepartment of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
D HallahanDepartment of Radiation Oncology, Washington University School of Medicine, St Louis, MO, USA.
Z Han1] Department of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, TN, USA [2] Department of Cancer Biology, Vanderbilt University School of Medicine, Nashville, TN, USA [3] Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN, USA.
Vanderbilt University · USCleveland Clinic Lerner College of Medicine · USWashington University in St. Louis · US

Funding

Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
Vanderbilt In Vivo Cellular and Molecular Imaging CenterP50CA128323 · NCI · VANDERBILT UNIVERSITY · PI SHYR, YU · 2008 to 2012
$6.8M
X-ray Targeted Therapeutic Genes within NanoparticlesR01CA125757 · NCI · WASHINGTON UNIVERSITY · PI HALLAHAN, DENNIS E · 2007 to 2011
$1.7M
Pharmacodynamic Assessment of RTK Inhibitors in CancerR01CA112385 · NCI · WASHINGTON UNIVERSITY · PI HALLAHAN, DENNIS E · 2005 to 2009
$1.3M
Roles of TIP-1 in Cancer RadiotherapyR01CA127482 · NCI · VANDERBILT UNIVERSITY · PI HAN, ZHAOZHONG · 2008 to 2011
$1.1M
NCATS NIH HHS UL1 TR000448NCI NIH HHS P50 CA128323NCI NIH HHS R01 CA112385NCI NIH HHS R01CA112385NCI NIH HHS R01 CA125757NCI NIH HHS R01 CA127482NCI NIH HHS R01CA127482
6 · The paper itself

Abstract

PDZ domains represent one group of the major structural units that mediate protein interactions in intercellular contact, signal transduction and assembly of biological machineries. Tax-interacting protein (TIP)-1 protein is composed of a single PDZ domain that distinguishes TIP-1 from other PDZ domain proteins that more often contain multiple protein domains and function as scaffolds for protein complex assembly. However, the biological functions of TIP-1, especially in cell transformation and tumor progression, are still controversial as observed in a variety of cell types. In this study, we have identified ARHGEF7, a guanine nucleotide exchange factor for Rho GTPases, as one novel TIP-1-interacting protein in human glioblastoma cells. We found that the presence of TIP-1 protein is essential to the intracellular redistribution of ARHGEF7 and rhotekin, one Rho effector and the spatiotemporally coordinated activation of Rho GTPases (RhoA, Cdc42 and Rac1) in migrating glioblastoma cells. TIP-1 knockdown resulted in both aberrant localization of ARHGEF7 and rhotekin, as well as abnormal activation of Rho GTPases that was accompanied with impaired motility of glioblastoma cells. Furthermore, TIP-1 knockdown suppressed tumor cell dispersal in orthotopic glioblastoma murine models. We also observed high levels of TIP-1 expression in human glioblastoma specimens, and the elevated TIP-1 levels are associated with advanced staging and poor prognosis in glioma patients. Although more studies are needed to further dissect the mechanism(s) by which TIP-1 modulates the intracellular redistribution and activation of Rho GTPases, this study suggests that TIP-1 holds potential as both a prognostic biomarker and a therapeutic target of malignant gliomas.

Indexed as

AnimalsApoptosis Regulatory Proteinsbeta CateninBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticEnzyme ActivationFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlioblastomaGTP-Binding ProteinsHumansIntracellular Signaling Peptides and ProteinsApoptosis Regulatory ProteinsARHGEF7 protein, humanbeta CateninGTP-Binding ProteinsIntracellular Signaling Peptides and Proteinsrho GTP-Binding ProteinsRho Guanine Nucleotide Exchange FactorsRTKN protein, humanTAX1BP3 protein, human

Identifiers

PMID23563176
PMCPMC3965267
OpenAlexW2067381358

What OpenQuestion holds

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Registered trials

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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.