Evidence map›Paper›PMID 11791178›Full record

ArticleOncogene2002

Autocrine heregulin generates growth factor independence and blocks apoptosis in colon cancer cells.

Srinivas Venkateswarlu, Dawn M Dawson, Patricia St Clair, Anjana Gupta, James K V Willson, Michael G Brattain

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 75 citations in OpenAlex.

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  15. Challenging issues in molecular-targeted therapy.Therapeutics and clinical risk management · 2009
    Article
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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

6 authors at 2 institutions in 1 country.

Srinivas VenkateswarluDepartment of Surgery, University of Texas Health Science Center at San Antonio, Texas, TX 78284, USA.
Dawn M Dawson
Patricia St Clair
Anjana Gupta
James K V Willson
Michael G Brattain
The University of Texas Health Science Center at San Antonio · USCase Western Reserve University · US

Funding

HETEROGENEITY OF HUMAN COLONIC CARCINOMAR01CA034432 · NCI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI BRATTAIN, MICHAEL G · 1985 to 2013
$3.8M
Cell Survival Determinants of Metastasis in IGF1R-Dependent CRCR01CA054807 · NCI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI BLACK, JENNIFER D. · 1991 to 2016
$3.7M
TGF BETA ROLE IN COLON CANCERR01CA068316 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WILLSON, JAMES K. · 1995 to 2002
$944k
ERBB2 KINASE SIGNALING IN COLON CARCINOGENESISK08CA084337 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI DAWSON, DAWN M · 2000 to 2005
$635k
NCI NIH HHS CA 34432NCI NIH HHS CA 54807NCI NIH HHS CA 68316NCI NIH HHS CA84337-01A1
6 · The paper itself

Abstract

The aim of this study was to determine whether constitutive ErbB2 activation controls growth and apoptosis in colon cancer cells. Growth arrested GEO cells showed constitutive activation of ErbB2 in the absence of exogenous growth factors or serum supplementation. Higher levels of heregulin and ErbB2 activation were observed in the growth-arrested state and cell cycle re-entry was independent of exogenous growth factors. Blockade of ErbB2 activation by heregulin neutralizing antibodies and by AG879 resulted in prevention of cell cycle re-entry. This indicated that autocrine heregulin activity was responsible for growth factor independence and for cell cycle re-entry. Activation of ErbB2 was the result of heregulin mediated interaction with ErbB3 and generated downstream activation of the ERK and the PI3K/AKT pathways. Heregulin neutralizing antibody treatment of growth arrested GEO cells also generated apoptosis as reflected by PARP cleavage and DNA fragmentation indicating a cell survival signal was also induced by the constitutively activated ErbB2. The activation of AKT but not the MAPK pathway was responsible for cell survival in these cells.

Indexed as

Autocrine CommunicationAdenocarcinomaApoptosisCell CycleChromonesColonic NeoplasmsCulture MediaCulture Media, Serum-FreeDimerizationDNA FragmentationEnzyme ActivationEnzyme InhibitorsFlavonoidsGene Expression Regulation, NeoplasticGenes, erbB-2Growth Substances2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneChromonesCulture MediaCulture Media, Serum-FreeEnzyme InhibitorsFlavonoidsGrowth SubstancesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein KinasesMorpholinesNeoplasm ProteinsNeuregulin-1Phosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsPoly(ADP-ribose) PolymerasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-aktReceptor, ErbB-3SirolimusTransforming Growth Factor alpha

Identifiers

PMID11791178
OpenAlexW2326300557

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.