Evidence map›Paper›PMID 19478945›Full record

ArticlePloS one2009

Molecular signatures of prostate stem cells reveal novel signaling pathways and provide insights into prostate cancer.

Roy Blum, Rashmi Gupta, Patricia E Burger, Christopher S Ontiveros, Sarah N Salm, Xiaozhong Xiong, Alexander Kamb, Holger Wesche, Lisa Marshall, Gene Cutler and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 69 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

14 authors at 5 institutions in 2 countries.

Roy BlumDepartment of Cell Biology, New York University School of Medicine, New York, New York, United States of America.
Rashmi Gupta
Patricia E Burger
Christopher S Ontiveros
Sarah N Salm
Xiaozhong Xiong
Alexander Kamb
Holger Wesche
Lisa Marshall
Gene Cutler
Xiangyun Wang
Jiri Zavadil
David Moscatelli
E Lynette Wilson
Amgen (United States) · USNew York University · USUniversity of Cape Town · ZABorough of Manhattan Community College · USNYU Langone Health · US

Funding

The Biology of Prostate Stem Cells - Resubmission - 1R01CA132641 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WILSON, ELAINE LYNETTE · 2007 to 2017
$4.0M
Angiopoietins in Prostate Biology and DiseaseR01CA090593 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MOSCATELLI, DAVID A · 2002 to 2005
$1.2M
The role of Wnt signaling in prostate homeostasisF32DK071468 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ONTIVEROS, CHRISTOPHER S · 2005 to 2007
$114k
NCI NIH HHS CA132641NCI NIH HHS CA 90593NCI NIH HHS R01 CA090593NCI NIH HHS R01 CA132641NIDDK NIH HHS 5F32DK071468NIDDK NIH HHS F32 DK071468
6 · The paper itself

Abstract

backgroundThe global gene expression profiles of adult and fetal murine prostate stem cells were determined to define common and unique regulators whose misexpression might play a role in the development of prostate cancer. METHODOLOGY/PRINCIPAL

findingsA distinctive core of transcriptional regulators common to both fetal and adult primitive prostate cells was identified as well as molecules that are exclusive to each population. Elements common to fetal and adult prostate stem cells include expression profiles of Wnt, Shh and other pathways identified in stem cells of other organs, signatures of the aryl-hydrocarbon receptor, and up-regulation of components of the aldehyde dehydrogenase/retinoic acid receptor axis. There is also a significant lipid metabolism signature, marked by overexpression of lipid metabolizing enzymes and the presence of the binding motif for Srebp1. The fetal stem cell population, characterized by more rapid proliferation and self-renewal, expresses regulators of the cell cycle, such as E2f, Nfy, Tead2 and Ap2, at elevated levels, while adult stem cells show a signature in which TGF-beta has a prominent role. Finally, comparison of the signatures of primitive prostate cells with previously described profiles of human prostate tumors identified stem cell molecules and pathways with deregulated expression in prostate tumors including chromatin modifiers and the oncogene, Erg. CONCLUSIONS/SIGNIFICANCE: Our data indicate that adult prostate stem or progenitor cells may acquire characteristics of self-renewing primitive fetal prostate cells during oncogenesis and suggest that aberrant activation of components of prostate stem cell pathways may contribute to the development of prostate tumors.

Indexed as

Signal TransductionAdultAnimalsCell ProliferationFetusGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiceMice, Inbred C57BLModels, BiologicalMultigene FamilyPromoter Regions, GeneticProstateProstatic NeoplasmsReceptors, Aryl HydrocarbonRNA, MessengerTranscription FactorsTransforming Growth Factor beta

Identifiers

PMID19478945
PMCPMC2684642
OpenAlexW1967456673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.