Evidence map›Paper›PMID 23774217›Full record

ArticleCancer research2013

RHPN2 drives mesenchymal transformation in malignant glioma by triggering RhoA activation.

Carla Danussi, Uri David Akavia, Francesco Niola, Andreja Jovic, Anna Lasorella, Dana Pe'er, Antonio Iavarone

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.7field-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

38 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. [RHPN2 is highly expressed in osteosarcoma cells to promote cell proliferation and migration and inhibit apoptosis].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  6. Pathway Analysis for Cancer Research and Precision Oncology Applications.Advances in experimental medicine and biology · 2022
    Article
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  19. Review
  20. Profiling the Mutational Landscape in Known Driver Genes and Novel Genes in African American Non-Small Cell Lung Cancer Patients.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    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

7 authors at 2 institutions in 1 country.

Carla DanussiInstitute for Cancer Genetics, Columbia University Medical Center, New York, NY 10032, USA.
Uri David Akavia
Francesco Niola
Andreja Jovic
Anna Lasorella
Dana Pe'er
Antonio Iavarone
Cancer Genetics (United States) · USColumbia University Irving Medical Center · US

Funding

Nation Center: Multi-Scale Study- Cellular Networks(RMI)U54CA121852 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2015
$37.4M
CATEGORY A: COMMUNITIES PUTTING PREVENTION TO WORKU58DP002414 · DP · WISCONSIN DEPARTMENT OF HEALTH SERVICES · PI UTTECH, SUSAN · 2010 to 2010
$7.8M
ID2 IN CELL CYCLE REGULATION AND CANCERR01CA085628 · NCI · YESHIVA UNIVERSITY · PI IAVARONE, ANTONIO · 2000 to 2010
$3.8M
The role of Id proteins in tumor development and angiogenesis in the brainR01CA101644 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LASORELLA, ANNA · 2003 to 2013
$3.5M
Computational analysis of Human High Grade GliomasR01NS061776 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IAVARONE, ANTONIO · 2009 to 2013
$2.4M
The role of the LZTR1 ubiquitin ligase in stem cells and cancerR01CA190891 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IAVARONE, ANTONIO · 2015 to 2019
$1.9M
Integrative Cancer Genomics: Drivers, Pathways and DrugsR01CA164729 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PE'ER, DANA · 2012 to 2016
$1.9M
Mechanisms and regulation of post-translational modifications of Id proteinsR01CA127643 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI IAVARONE, ANTONIO · 2008 to 2012
$1.7M
The Ureb-1 ubiquitin ligase in neural stem cells and cancerR01CA131126 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LASORELLA, ANNA · 2008 to 2012
$1.6M
NCCDPHP CDC HHS DP20D2414-1NCI NIH HHS 5U54CA121852-08NCI NIH HHS CA164729-01NCI NIH HHS R01 CA085628NCI NIH HHS R01CA085628NCI NIH HHS R01 CA101644NCI NIH HHS R01CA101644NCI NIH HHS R01 CA127643NCI NIH HHS R01CA127643NCI NIH HHS R01 CA131126NCI NIH HHS R01CA131126NCI NIH HHS R01 CA164729NCI NIH HHS R01 CA190891NCI NIH HHS U54 CA121852NINDS NIH HHS R01 NS061776NINDS NIH HHS R01NS061776
6 · The paper itself

Abstract

Mesenchymal transformation is a hallmark of aggressive glioblastoma (GBM). Here, we report the development of an unbiased method for computational integration of copy number variation, expression, and mutation data from large datasets. Using this method, we identified rhophilin 2 (RHPN2) as a central genetic determinant of the mesenchymal phenotype of human GBM. Notably, amplification of the human RHPN2 gene on chromosome 19 correlates with a dramatic decrease in the survival of patients with glioma. Ectopic expression of RHPN2 in neural stem cells and astrocytes triggered the expression of mesenchymal genes and promoted an invasive phenotype without impacting cell proliferation. Mechanistically, these effects were implemented through RHPN2-mediated activation of RhoA, a master regulator of cell migration and invasion. Our results define RHPN2 amplification as a central genetic determinant of a highly aggressive phenotype that directs the worst clinical outcomes in patients with GBM.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAstrocytesCell Growth ProcessesCell Line, TumorCell MovementCell Transformation, NeoplasticChromosomes, Human, Pair 19DNA Copy Number VariationsGene Expression Regulation, NeoplasticGlioblastomaHEK293 CellsHumansMesenchymal Stem CellsMiceMutationAdaptor Proteins, Signal TransducingrhoA GTP-Binding ProteinRHPN2 protein, human

Identifiers

PMID23774217
PMCPMC3805507
OpenAlexW2119908855

What OpenQuestion holds

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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.