Evidence map›Paper›PMID 28112153›Full record

ArticleNature communications2017

Dissecting cell-type-specific roles of androgen receptor in prostate homeostasis and regeneration through lineage tracing.

Qing Xie, Yueli Liu, Tao Cai, Corrigan Horton, Joshua Stefanson, Zhu A Wang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Review
  3. RUNX1T1 drives stem-like small-cell neuroendocrine prostate cancer identity.Frontiers in cell and developmental biology · 2026
    Article
  4. Review
  5. Cellular cartography reveals mouse prostate organization and determinants of castration resistance.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Prostate organogenesis.Development (Cambridge, England) · 2022
    Article
  20. Article
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 2 countries.

Qing XieDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
Yueli LiuDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
Tao CaiSequencing Center, National Institute of Biological Sciences, Beijing 102206, China.
Corrigan HortonDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
Joshua StefansonDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
Zhu A WangDepartment of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, California 95064, USA.
University of California, Santa Cruz · USNational Institute of Biological Sciences, Beijing · CN

Funding

Regulation of prostate epithelial basal cell plasticityR01GM116872 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI WANG, ZHU · 2015 to 2019
$1.8M
NIGMS NIH HHS R01 GM116872
6 · The paper itself

Abstract

Androgen signals through androgen receptor (AR) to influence prostate development and cancer. How stromal and epithelial AR regulate prostate homeostasis remains unclear. Using genetic lineage tracing, we systematically investigated the role of cell-autonomous AR in different prostate epithelial cell types. Here we show that AR is dispensable for basal cell maintenance, but is cell-autonomously required for the luminal differentiation of rare basal stem cells. In contrast, AR deletion in luminal cells alters cell morphology and induces transient over-proliferation, without affecting androgen-mediated luminal cell survival or regeneration. However, AR is selectively required for the maintenance of daughter cells produced by castration-resistant Nkx3.1-expressing luminal stem cells (CARNs). Notably, Pten loss can override AR-loss effects in both basal and luminal compartments to initiate tumours. Our data reveal distinct cell-type-specific roles of epithelial AR in orchestrating prostate homeostasis, and question the notion that epithelial AR serves as a tumour suppressor in early cancer initiation.

Indexed as

AnimalsGene Expression RegulationGenotypeMaleMiceMice, TransgenicOrchiectomyOrganoidsPrincipal Component AnalysisProstateReceptors, AndrogenSelective Estrogen Receptor ModulatorsTamoxifenTissue Culture TechniquesReceptors, AndrogenSelective Estrogen Receptor ModulatorsTamoxifen

Identifiers

PMID28112153
PMCPMC5264212
OpenAlexW2581724956

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.