Evidence map›Paper›PMID 21739465›Full record

ArticleThe Prostate2012

Altered prostate epithelial development in mice lacking the androgen receptor in stromal fibroblasts.

Shengqiang Yu, Chiuan-Ren Yeh, Yuanjie Niu, Hong-Chiang Chang, Yu-Chieh Tsai, Harold L Moses, Chih-Rong Shyr, Chawnshang Chang, Shuyuan Yeh

Open access · greenAbstract read
In one paragraph

Article in The Prostate, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
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  14. Prostate organogenesis.Development (Cambridge, England) · 2022
    Article
  15. Article
  16. Role of prostate stem cells and treatment strategies in benign prostate hyperplasia.American journal of clinical and experimental urology · 2022
    Review
  17. 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

9 authors at 5 institutions in 3 countries.

Shengqiang YuGeorge Whipple Lab for Cancer Research, Departments of Pathology and Urology, The Wilmot Cancer Center, University of Rochester Medical Center, Rochester, New York 14642, USA.
Chiuan-Ren Yeh
Yuanjie Niu
Hong-Chiang Chang
Yu-Chieh Tsai
Harold L Moses
Chih-Rong Shyr
Chawnshang Chang
Shuyuan Yeh
University of Rochester Medical Center · USChina Medical University · TWChina Medical University Hospital · TWTianjin Medical University · CNVanderbilt University · US

Funding

Loss of Androgen Receptor Promotes Metastatic Prostate CancerR01CA122840 · NCI · UNIVERSITY OF ROCHESTER · PI CHANG, CHAWNSHANG, YEH, SHUYUAN · 2007 to 2011
$1.5M
MAP Kinase Signal on AR and AR coregulatorsR01DK060912 · NIDDK · UNIVERSITY OF ROCHESTER · PI YEH, SHUYUAN · 2001 to 2004
$1.1M
NCI NIH HHS CA122840NCI NIH HHS R01 CA122840NIDDK NIH HHS DK60912NIDDK NIH HHS R01 DK060912
6 · The paper itself

Abstract

backgroundAndrogens and the androgen receptor (AR) play important roles in the development of male urogenital organs. We previously found that mice with total AR knockout (ARKO) and epithelial ARKO failed to develop normal prostate with loss of differentiation. We have recently knocked out AR gene in smooth muscle cells and found the reduced luminal infolding and IGF-1 production in the mouse prostate. However, AR roles of stromal fibroblasts in prostate development remain unclear.

methodsTo further probe the stromal fibroblast AR roles in prostate development, we generated tissue-selective knockout mice with the AR gene deleted in stromal fibroblasts (FSP-ARKO). We also used primary culture stromal cells to confirm the in vivo data and investigate mechanisms related to prostate development.

resultsThe results showed cellular alterations in the FSP-ARKO mouse prostate with decreased epithelial proliferation, increased apoptosis, and decreased collagen composition. Further mechanistic studies demonstrated that FSP-ARKO mice have defects in the expression of prostate stromal growth factors. To further confirm these in vivo findings, we prepared primary cultured mouse prostate stromal cells and found knocking down the stromal AR could result in growth retardation of prostate stromal cells and co-cultured prostate epithelial cells, as well as decrease of some stromal growth factors.

conclusionsOur FSP-ARKO mice not only provide the first in vivo evidence in Cre-loxP knockout system for the requirement of stromal fibroblast AR to maintain the normal development of the prostate, but may also suggest the selective knockdown of stromal AR might become a potential therapeutic approach to battle prostate hyperplasia and cancer.

Indexed as

Cell ProliferationAnimalsApoptosisCell CommunicationCell DifferentiationCells, CulturedCoculture TechniquesCollagenEpithelial CellsFibroblastsIntercellular Signaling Peptides and ProteinsMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicCollagenIntercellular Signaling Peptides and ProteinsReceptors, AndrogenTestosterone

Identifiers

PMID21739465
PMCPMC4402036
OpenAlexW2149464366

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.