Evidence map›Paper›PMID 30982770›Full record

ArticleCell stem cell2019

Spatially Restricted Stromal Wnt Signaling Restrains Prostate Epithelial Progenitor Growth through Direct and Indirect Mechanisms.

Xing Wei, Li Zhang, Zhicheng Zhou, Oh-Joon Kwon, Yiqun Zhang, Hoang Nguyen, Ruth Dumpit, Lawrence True, Peter Nelson, Baijun Dong and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2019. 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
10.2field-weighted citation impact, top 1% 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, 68 citations in OpenAlex.

  1. Review
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  9. Enhanced prostatic Esr1The Journal of pathology · 2024
    Article
  10. Article
  11. Telocytes of the male reproductive system: dynamic tissue organizers.Frontiers in cell and developmental biology · 2024
    Review
  12. Article
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  15. 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

17 authors at 7 institutions in 5 countries.

Xing WeiDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Graduate Program in Integrative Molecular and Biomedical Sciences, Baylor College of Medicine, Houston, TX 77030, USA; Department of Urology, University of Washington, Seattle, WA 98109, USA.
Li ZhangDepartment of Urology, University of Washington, Seattle, WA 98109, USA.
Zhicheng ZhouDepartment of Urology, University of Washington, Seattle, WA 98109, USA.
Oh-Joon KwonDepartment of Urology, University of Washington, Seattle, WA 98109, USA.
Yiqun ZhangDan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Hoang NguyenDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center of Stem Cell and Regenerative Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Ruth DumpitHuman Biology Division, Fred Hutch Cancer Research Center, Seattle, WA 98109, USA.
Lawrence TrueDepartment of Pathology, University of Washington, Seattle, WA 98109, USA.
Peter NelsonHuman Biology Division, Fred Hutch Cancer Research Center, Seattle, WA 98109, USA.
Baijun DongDepartment of Urology, RenJi Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Wei XueDepartment of Urology, RenJi Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Walter BirchmeierMax Delbrück Center for Molecular Medicine (MDC), Robert-Rössle-Str. 10, 13092 Berlin, Germany.
Makoto M TaketoDivision of Experimental Therapeutics, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Feng XuInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
Chad J CreightonDan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA; Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Michael M IttmannDan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX 77030, USA; Michael E. DeBakey Department of Veterans Affairs Medical Center, Houston, TX 77030, USA.
Li XinDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Department of Urology, University of Washington, Seattle, WA 98109, USA; Institute of Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA. Electronic address: xin18@uw.edu.
Baylor College of Medicine · USUniversity of Washington · USFred Hutch Cancer Center · USShanghai Jiao Tong University · CNInstitute of Molecular and Cell Biology · SGKyoto University · JPMax Delbrück Center · DE

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Virology CoreP30AI036211 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI BUTEL, JANET S · 1994 to 2015
$21.7M
Molecular Mechanisms of Initiation of Benign Prostatic HyperplasiaR01DK107436 · NIDDK · UNIVERSITY OF WASHINGTON · PI XIN, LI · 2016 to 2024
$4.4M
The Prostate Epithelial Cell Lineage HierarchyR01DK092202 · NIDDK · UNIVERSITY OF WASHINGTON · PI XIN, LI · 2011 to 2019
$3.2M
The Notch Signaling in Prostate Homeostasis and CarcinogenesisR01CA190378 · NCI · UNIVERSITY OF WASHINGTON · PI XIN, LI · 2015 to 2019
$1.9M
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
Reprogramming of Prostate Stromal Cells by Prostate InflammationR21CA196570 · NCI · BAYLOR COLLEGE OF MEDICINE · PI XIN, LI · 2016 to 2017
$408k
NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA190378NCI NIH HHS R21 CA196570NCRR NIH HHS S10 RR024574NIAID NIH HHS P30 AI036211NIDDK NIH HHS R01 DK092202NIDDK NIH HHS R01 DK107436
6 · The paper itself

Abstract

Cell-autonomous Wnt signaling has well-characterized functions in controlling stem cell activity, including in the prostate. While niche cells secrete Wnt ligands, the effects of Wnt signaling in niche cells per se are less understood. Here, we show that stromal cells in the proximal prostatic duct near the urethra, a mouse prostate stem cell niche, not only produce multiple Wnt ligands but also exhibit strong Wnt/β-catenin activity. The non-canonical Wnt ligand Wnt5a, secreted by proximal stromal cells, directly inhibits proliefration of prostate epithelial stem or progenitor cells whereas stromal cell-autonomous canonical Wnt/β-catenin signaling indirectly suppresses prostate stem or progenitor activity via the transforming growth factor β (TGFβ) pathway. Collectively, these pathways restrain the proliferative potential of epithelial cells in the proximal prostatic ducts. Human prostate likewise exhibits spatially restricted distribution of stromal Wnt/β-catenin activity, suggesting a conserved mechanism for tissue patterning. Thus, this study shows how distinct stromal signaling mechanisms within the prostate cooperate to regulate tissue homeostasis.

Indexed as

Animalsbeta CateninCell ProliferationCells, CulturedEpithelial CellsHumansMaleMiceMice, Inbred C57BLMice, SCIDProstateReceptor Cross-TalkStem Cell NicheStem CellsStromal CellsTransforming Growth Factor betabeta CateninTransforming Growth Factor betaWnt-5a Proteinprostate stem cellsstem cell nichestromal-epithelial interactionTGFβWnt

Identifiers

PMID30982770
PMCPMC6548441
OpenAlexW2938525919

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.