Evidence map›Paper›PMID 29059167›Full record

ArticleOncogene2018

Loss of RhoA promotes skin tumor formation and invasion by upregulation of RhoB.

A García-Mariscal, H Li, E Pedersen, K Peyrollier, K M Ryan, A Stanley, F Quondamatteo, C Brakebusch

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
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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

8 authors at 3 institutions in 3 countries.

A García-MariscalBiotech Research and Innovation Centre, BRIC, University of Copenhagen, Copenhagen, Denmark.
H LiBiotech Research and Innovation Centre, BRIC, University of Copenhagen, Copenhagen, Denmark.
E PedersenBiotech Research and Innovation Centre, BRIC, University of Copenhagen, Copenhagen, Denmark.
K PeyrollierBiotech Research and Innovation Centre, BRIC, University of Copenhagen, Copenhagen, Denmark.
K M RyanBeatson Institute, Glasgow, UK.
A StanleySkin and Extracellular Matrix Research Group, Anatomy, NUI, Galway, Ireland.
F QuondamatteoSkin and Extracellular Matrix Research Group, Anatomy, NUI, Galway, Ireland.
C BrakebuschBiotech Research and Innovation Centre, BRIC, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKOllscoil na Gaillimhe – University of Galway · IECancer Research UK Scotland Institute · GB

Funding

Cancer Research UK 15816Cancer Research UK 22903
6 · The paper itself

Abstract

Cellular movement is controlled by small GTPases, such as RhoA. Although migration is crucial for cancer cell invasion, the specific role of RhoA in tumor formation is unclear. Inducing skin tumors in mice with a keratinocyte-restricted loss of RhoA, we observed increased tumor frequency, growth and invasion. In vitro invasion assays revealed that in the absence of RhoA cell invasiveness is increased in a Rho-associated protein kinase (ROCK) activation and cell contraction-dependent manner. Surprisingly, loss of RhoA causes increased Rho signaling via overcompensation by RhoB because of reduced lysosomal degradation of RhoB in Gamma-aminobutyric acid receptor-associated protein (GABARAP)+ autophagosomes and endosomes. In the absence of RhoA, RhoB relocalized to the plasma membrane and functionally replaced RhoA with respect to invasion, clonogenic growth and survival. Our data demonstrate for the first time that RhoA is a tumor suppressor in 7,12-dimethylbenz[a]anthracene/12-O-tetradecanoylphorbol 13-acetate skin carcinogenesis and identify Rho signaling dependent on RhoA and RhoB as a potent driver of tumor progression.

Indexed as

AnimalsAnthracenesApoptosisBiomarkers, TumorCell MovementCell ProliferationCells, CulturedHumansKeratinocytesLysosomesMiceMice, Inbred C57BLNeoplasm InvasivenessPiperidinesPrognosisrhoA GTP-Binding Protein3-(2,6-bis(4-fluorophenyl)-3-methylpiperidin-4-ylideneamino)-2-thioxoimidazolidin-4-one on 7,12-dimethylbenz(a)anthraceneAnthracenesBiomarkers, TumorPiperidinesrhoA GTP-Binding Proteinrho-Associated KinasesrhoB GTP-Binding ProteinrhoC GTP-Binding Protein

Identifiers

PMID29059167
OpenAlexW2765134073

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.