Evidence map›Paper›PMID 22786680›Full record

ArticleScience translational medicine2012

Matrix metalloproteinase induction of Rac1b, a key effector of lung cancer progression.

Melody L Stallings-Mann, Jens Waldmann, Ying Zhang, Erin Miller, Mona L Gauthier, Daniel W Visscher, Gregory P Downey, Evette S Radisky, Alan P Fields, Derek C Radisky

Abstract read
In one paragraph

Article in Science translational medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

68 citing papers in PubMed, 112 citations in OpenAlex.

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  5. A TIAM1-TRIM28 complex mediates epigenetic silencing of protocadherins to promote migration of lung cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
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8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Melody L Stallings-MannDepartment of Cancer Biology, Mayo Clinic Cancer Center, Jacksonville, FL 32224, USA. stallingsmann.melody@mayo.edu
Jens Waldmann
Ying Zhang
Erin Miller
Mona L Gauthier
Daniel W Visscher
Gregory P Downey
Evette S Radisky
Alan P Fields
Derek C Radisky
Mayo Clinic in Florida · USUniversity of Colorado Denver · US

Funding

Three-Dimensional Organoid Cultures to Investigate 3q26 Driver Functions in Multiple Lung Cancer Cells of OriginR01CA081436 · NCI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI FIELDS, ALAN P. · 1999 to 2022
$9.9M
Focal Adhesion Modulation of IL-1 Signaling: Importance in Pulmonary FibrosisR01HL090669 · NHLBI · NATIONAL JEWISH HEALTH · PI DOWNEY, GREGORY PAUL · 2008 to 2011
$1.8M
Mechanisms of MMP-Induced Malignancy in Breast CellsR01CA122086 · NCI · MAYO CLINIC JACKSONVILLE · PI RADISKY, DEREK C · 2007 to 2011
$1.4M
In Vitro Synthesis of Fibrosis GenesisR21CA128660 · NCI · PRINCETON UNIVERSITY · PI NELSON, CELESTE M · 2007 to 2008
$339k
NCI NIH HHS CA081436NCI NIH HHS CA122086NCI NIH HHS CA128660NCI NIH HHS R01 CA081436NCI NIH HHS R01 CA122086NCI NIH HHS R21 CA128660NHLBI NIH HHS HL090669NHLBI NIH HHS R01 HL090669
6 · The paper itself

Abstract

Lung cancer is more deadly than colon, breast, and prostate cancers combined, and treatment improvements have failed to improve prognosis significantly. Here, we identify a critical mediator of lung cancer progression, Rac1b, a tumor-associated protein with cell-transforming properties that are linked to the matrix metalloproteinase (MMP)-induced epithelial-mesenchymal transition (EMT) in lung epithelial cells. We show that expression of mouse Rac1b in lung epithelial cells of transgenic mice stimulated EMT and spontaneous tumor development and that activation of EMT by MMP-induced expression of Rac1b gave rise to lung adenocarcinoma in the transgenic mice through bypassing oncogene-induced senescence. Rac1b is expressed abundantly in stages 1 and 2 of human lung adenocarcinomas and, hence, is an attractive molecular target for the development of new therapies that prevent progression to later-stage lung cancers.

Indexed as

Disease ProgressionAdenocarcinomaAdenocarcinoma of LungAdenomaAgingAnimalsCell Line, TumorCells, CulturedEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansLung NeoplasmsMatrix Metalloproteinase 3MesodermMiceMice, TransgenicMatrix Metalloproteinase 3Neuropeptidesrac1 GTP-Binding ProteinRAC1 protein, humanRac1 protein, mouserac GTP-Binding ProteinsVimentin

Identifiers

PMID22786680
PMCPMC3733503
OpenAlexW2032304802

What OpenQuestion holds

Textmetadata
LicenceTDM
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.