Evidence map›Paper›PMID 11134071›Full record

ArticleThe Journal of cell biology2000

Dual stimulation of Ras/mitogen-activated protein kinase and RhoA by cell adhesion to fibronectin supports growth factor-stimulated cell cycle progression.

E H Danen, P Sonneveld, A Sonnenberg, K M Yamada

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 116 citations in OpenAlex.

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  8. Theranostics · 2017
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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

4 authors at 2 institutions in 2 countries.

E H DanenDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands. edanen@nki.nl
P Sonneveld
A Sonnenberg
K M Yamada
The Netherlands Cancer Institute · NLNational Institute of Dental and Craniofacial Research · US

Funding

Craniofacial Developmental DynamicsZIADE000525 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH · 2009 to 2025
$14.5M
Cell-Matrix Interactions and MigrationZIADE000524 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH · 2009 to 2025
$10.2M
SALIVARY GLAND SECRETORY MECHANISMS DURING NORMAL AND ALTERED FUNCTIONAL STATESZ01DE000336 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI BAUM, BRUCE J · 1985 to 2008
$7.0M
Salivary Gland Secretion Mechanisms During Normal And Altered Functional StatesZIADE000336 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI BAUM, BRUCE J · 2009 to 2011
$5.9M
REGULATION OF CELL ADHESION, MIGRATION, AND MORPHOGENESISZ01DE000525 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH MANAO · 1991 to 2008
$1.5M
INTEGRIN RECEPTOR FUNCTION AND SIGNALINGZ01DE000524 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH MANAO · 1991 to 2008
$1.5M
6 · The paper itself

Abstract

In cellular transformation, activated forms of the small GTPases Ras and RhoA can cooperate to drive cells through the G1 phase of the cell cycle. Here, we show that a similar but substrate-regulated mechanism is involved in the anchorage-dependent proliferation of untransformed NIH-3T3 cells. Among several extracellular matrix components tested, only fibronectin supported growth factor-induced, E2F-dependent S phase entry. Although all substrates supported the mitogen-activated protein kinase (MAPK) response to growth factors, RhoA activity was specifically enhanced on fibronectin. Moreover, induction of cyclin D1 and suppression of p21(Cip/Waf) occurred specifically, in a Rho-dependent fashion, in cells attached to fibronectin. This ability of fibronectin to stimulate both Ras/MAPK- and RhoA-dependent signaling can explain its potent cooperation with growth factors in the stimulation of cell cycle progression.

Indexed as

Carrier ProteinsCell Cycle ProteinsDNA-Binding Proteins3T3 CellsActinsAnimalsCell AdhesionCell CycleCulture Media, Serum-FreeCyclin D1Cyclin-Dependent Kinase Inhibitor p21CyclinsCytoskeletonE2F Transcription FactorsEnzyme ActivationFibronectinsActinsArid4a protein, mouseCarrier ProteinsCdkn1a protein, mouseCell Cycle ProteinsCulture Media, Serum-FreeCyclin D1Cyclin-Dependent Kinase Inhibitor p21CyclinsDNA-Binding ProteinsE2F Transcription FactorsFibronectinsGrowth SubstancesMitogen-Activated Protein Kinasesras GTPase-Activating ProteinsRetinoblastoma-Binding Protein 1Retinoblastoma ProteinrhoA GTP-Binding ProteinRNA, MessengerTranscription Factor DP1Transcription Factors

Identifiers

PMID11134071
PMCPMC2150684
OpenAlexW2133415297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.