Evidence map›Paper›PMID 19143022›Full record

ArticleThe Prostate2009

EGFR ligand switch in late stage prostate cancer contributes to changes in cell signaling and bone remodeling.

Alyse M DeHaan, Natalie M Wolters, Evan T Keller, Kathleen M Woods Ignatoski

Open access · greenAbstract read
In one paragraph

Article in The Prostate, 2009. 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
2.5field-weighted citation impact, top 10% 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, 45 citations in OpenAlex.

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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 1 institution in 1 country.

Alyse M DeHaanDepartment of Urology, University of Michigan Health System, Ann Arbor, Michigan 48109-0654, USA.
Natalie M Wolters
Evan T Keller
Kathleen M Woods Ignatoski
Michigan Medicine · US

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KELLER, EVAN T · 2004 to 2024
$29.6M
Prostate Cancer Metastasis Suppressor: Role of RKIPR01CA098513 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KELLER, EVAN T · 2004 to 2008
$1.2M
NCI NIH HHS P01 CA093900NCI NIH HHS R01 CA098513
6 · The paper itself

Abstract

backgroundBone metastasis occurs frequently in advanced prostate cancer (PCa) patients; however, it is not known why this happens. The epidermal growth factor receptor (EGFR) ligand EGF is available to early stage PCa; whereas, TGF-alpha is available when PCa metastasizes. Since the microenvironment of metastases has been shown to play a role in the survival of the tumor, we examined whether the ligands had effects on cell survival and proliferation in early and late PCa.

methodsWe used LNCaP cells as a model of early stage, non-metastatic PCa and the isogenic C4-2B cells as a model of late stage, metastatic PCa.

resultsWe found that the proliferation factor MAPK and the survival factor AKT were differentially activated in the presence of different ligands. TGF-alpha induced growth of C4-2B cells and not of the parental LNCaP cells; however, LNCaP cells expressing a constitutively active AKT did proliferate with TGF-alpha. Therefore, AKT appeared to be the TGF-alpha-responsive factor for survival of the late stage PCa cells. LNCaP cells exposed to EGF produced more osteoprotegerin (OPG), an inhibitor of bone remodeling, than C4-2B cells with TGF-alpha, which had increased expression of RANKL, an activator of bone remodeling. In concordance, TGF-alpha-treated C4-2B conditioned medium was able to differentiate an osteoclast precursor line to a greater extent than EGF-treated C4-2B or TGF-alpha-treated LNCaP conditioned media.

conclusionThe switch in EGFR ligand availability as PCa progresses affects cell survival and contributes to bone remodeling.

Indexed as

AdenocarcinomaBone NeoplasmsBone RemodelingCell Line, TumorDisease ProgressionEpidermal Growth FactorErbB ReceptorsHumansLigandsMaleMitogen-Activated Protein Kinase KinasesModels, BiologicalNeoplasm StagingProstatic NeoplasmsProto-Oncogene Proteins c-aktRANK LigandEGFR protein, humanEpidermal Growth FactorErbB ReceptorsLigandsMitogen-Activated Protein Kinase KinasesProto-Oncogene Proteins c-aktRANK LigandTNFSF11 protein, humanTransforming Growth Factor alpha

Identifiers

PMID19143022
PMCPMC2766509
OpenAlexW2128742818

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.