Evidence map›Paper›PMID 26426536›Full record

ArticlePloS one2015

Ornithine Decarboxylase Activity Is Required for Prostatic Budding in the Developing Mouse Prostate.

Melissa Gamat, Rita L Malinowski, Linnea J Parkhurst, Laura M Steinke, Paul C Marker

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Polyamine metabolism in prostate cancer.Current opinion in oncology · 2025
    Review
  2. Review
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

5 authors at 1 institution in 1 country.

Melissa GamatSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, United States of America.
Rita L MalinowskiSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, United States of America.
Linnea J ParkhurstSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, United States of America.
Laura M SteinkeSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, United States of America.
Paul C MarkerSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI, United States of America.
University of Wisconsin–Madison · US

Funding

Role of Beta-Catenin in Urinary DysfunctionU54DK104310 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI MACOSKA, JILL A., MARKER, PAUL C · 2014 to 2023
$12.8M
Steroid hormones and SFRP1 in the age-related incidence of BPH and BOOR01DK091193 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI MARKER, PAUL C · 2011 to 2015
$1.6M
Novel prostate cancer oncogenes identified by transposon mutagenesisR01CA140217 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI MARKER, PAUL C · 2010 to 2014
$1.4M
NCI NIH HHS CA140217NCI NIH HHS R01 CA140217NIDDK NIH HHS DK091193NIDDK NIH HHS R01 DK091193NIDDK NIH HHS U54 DK104310
6 · The paper itself

Abstract

The prostate is a male accessory sex gland that produces secretions in seminal fluid to facilitate fertilization. Prostate secretory function is dependent on androgens, although the mechanism by which androgens exert their effects is still unclear. Polyamines are small cationic molecules that play pivotal roles in DNA transcription, translation and gene regulation. The rate-limiting enzyme in polyamine biosynthesis is ornithine decarboxylase, which is encoded by the gene Odc1. Ornithine decarboxylase mRNA decreases in the prostate upon castration and increases upon administration of androgens. Furthermore, testosterone administered to castrated male mice restores prostate secretory activity, whereas administering testosterone and the ornithine decarboxylase inhibitor D,L-α-difluromethylornithine (DFMO) to castrated males does not restore prostate secretory activity, suggesting that polyamines are required for androgens to exert their effects. To date, no one has examined polyamines in prostate development, which is also androgen dependent. In this study, we showed that ornithine decarboxylase protein was expressed in the epithelium of the ventral, dorsolateral and anterior lobes of the adult mouse prostate. Ornithine decarboxylase protein was also expressed in the urogenital sinus (UGS) epithelium of the male and female embryo prior to prostate development, and expression continued in prostatic epithelial buds as they emerged from the UGS. Inhibiting ornithine decarboxylase using DFMO in UGS organ culture blocked the induction of prostatic buds by androgens, and significantly decreased expression of key prostate transcription factor, Nkx3.1, by androgens. DFMO also significantly decreased the expression of developmental regulatory gene Notch1. Other genes implicated in prostatic development including Sox9, Wif1 and Srd5a2 were unaffected by DFMO. Together these results indicate that Odc1 and polyamines are required for androgens to exert their effect in mediating prostatic bud induction, and are required for the expression of a subset of prostatic developmental regulatory genes including Notch1 and Nkx3.1.

Indexed as

Gene Expression Regulation, DevelopmentalAndrogensAnimalsBlotting, WesternCells, CulturedEmbryo, MammalianFemaleFluorescent Antibody TechniqueImmunoenzyme TechniquesIn Situ HybridizationMaleMiceMice, Inbred C57BLOrganogenesisOrnithineOrnithine DecarboxylaseAndrogensOrnithineOrnithine DecarboxylaseRNA, Messenger

Identifiers

PMID26426536
PMCPMC4591331
OpenAlexW2297095656

What OpenQuestion holds

Textmetadata
LicenceCC0
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.