Evidence map›Paper›PMID 11094087›Full record

ArticleMolecular and cellular biology2000

Induced expression of Rnd3 is associated with transformation of polarized epithelial cells by the Raf-MEK-extracellular signal-regulated kinase pathway.

S H Hansen, M M Zegers, M Woodrow, P Rodriguez-Viciana, P Chardin, K E Mostov, M McMahon

Abstract read
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Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

43 citing papers in PubMed, 102 citations in OpenAlex.

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  18. Fractalkine-induced endothelial cell migration requires MAP kinase signaling.Pathobiology : journal of immunopathology, molecular and cellular biology · 2010
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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 2 countries.

S H HansenCancer Research Institute and Department of Cellular and Molecular Pharmacology, University of California San Francisco Cancer Center, San Francisco, California 94143, USA. hansen@bbri.org
M M Zegers
M Woodrow
P Rodriguez-Viciana
P Chardin
K E Mostov
M McMahon
Cancer Research Institute · USUniversity of California, San Francisco · USCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Madin-Darby canine kidney (MDCK) epithelial cells transformed by oncogenic Ras and Raf exhibit cell multilayering and alterations in the actin cytoskeleton. The changes in the actin cytoskeleton comprise a loss of actin stress fibers and enhanced cortical actin. Using MDCK cells expressing a conditionally active form of Raf, we have explored the molecular mechanisms that underlie these observations. Raf activation elicited a robust increase in Rac1 activity consistent with the observed increase in cortical actin. Loss of actin stress fibers is indicative of attenuated Rho function, but no change in Rho-GTP levels was detected following Raf activation. However, the loss of actin stress fibers in Raf-transformed cells was preceded by the induced expression of Rnd3, an endogenous inhibitor of Rho protein function. Expression of Rnd3 alone at levels equivalent to those observed following Raf transformation led to a substantial loss of actin stress fibers. Moreover, cells expressing activated RhoA failed to multilayer in response to Raf. Pharmacological inhibition of MEK activation prevented all of the biological and biochemical changes described above. Consequently, the data are consistent with a role for induced Rnd3 expression downstream of the Raf-MEK-extracellular signal-regulated kinase pathway in epithelial oncogenesis.

Indexed as

Cell Transformation, NeoplasticGene Expression RegulationSignal TransductionActinsAnimalsBlotting, WesternCadherinsCell FractionationCell LineCell PolarityCytoskeletonDogsEcdysoneEpithelial CellsEstrogen AntagonistsIntercellular JunctionsActinsafimoxifeneCadherinsEcdysoneEstrogen Antagonistsponesterone AProtein Serine-Threonine KinasesProto-Oncogene Proteins c-rafRecombinant Fusion Proteinsrho GTP-Binding ProteinsTamoxifen

Identifiers

PMID11094087
PMCPMC102193
OpenAlexW2114117271

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.