Evidence map›Paper›PMID 24731097›Full record

ArticleEndocrinology2014

Essential roles of epithelial bone morphogenetic protein signaling during prostatic development.

Akiko Omori, Shinichi Miyagawa, Yukiko Ogino, Masayo Harada, Kenichiro Ishii, Yoshiki Sugimura, Hajime Ogino, Naomi Nakagata, Gen Yamada

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Prostate Organogenesis.Cold Spring Harbor perspectives in medicine · 2018
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Histone acetylation regulates prostate ductal morphogenesis through a bone morphogenetic protein-dependent mechanism.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    Article
  7. Review
  8. 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

9 authors at 7 institutions in 1 country.

Akiko OmoriDepartment of Developmental Genetics (A.O., G.Y.), Institute of Advanced Medicine, Wakayama Medical University, Wakayama, 641-8509, Japan; Okazaki Institute for Integrative Bioscience (S.M., Y.O.), National Institute for Basic Biology, National Institutes of Natural Science, Okazaki, 444-8787, Japan; Department of Clinical Anatomy (M.H.), Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, 113-8591, Japan; Department of Oncologic Pathology (K.I.), and Nephro-Urologic Surgery and Andrology (Y.S.), Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan; Department of Animal Bioscience (H.O.), Nagahama Institute of Bio-Science and Technology, Nagahama, Shiga, 526-0829, Japan; and Division of Reproductive Engineering (N.N.), Center for Animal Resources and Development (CARD), Kumamoto University, Kumamoto 860-0811, Japan.
Shinichi Miyagawa
Yukiko Ogino
Masayo Harada
Kenichiro Ishii
Yoshiki Sugimura
Hajime Ogino
Naomi Nakagata
Gen Yamada
Mie University · JPWakayama Medical University · JPKumamoto University · JPNagahama Institute of Bio-Science and Technology · JPNational Institute for Basic Biology · JPNational Institutes of Natural Sciences · JPTokyo Medical and Dental University · JP

Funding

EXTERNAL GENITALIA DEVELOPMENT AND HYPOSPADIASR01ES016597 · NIEHS · WASHINGTON UNIVERSITY · PI MA, LIANG · 2009 to 2013
$1.5M
NIEHS NIH HHS R01 ES016597NIEHS NIH HHS R01ES016597-01A1
6 · The paper itself

Abstract

Prostate is a male sex-accessory organ. The prostatic epithelia consist primarily of basal and luminal cells that differentiate from embryonic urogenital sinus epithelia. Prostate tumors are believed to originate in the basal and luminal cells. However, factors that promote normal epithelial differentiation have not been well elucidated, particularly for bone morphogenetic protein (Bmp) signaling. This study shows that Bmp signaling prominently increases during prostatic differentiation in the luminal epithelia, which is monitored by the expression of phosphorylated Smad1/5/8. To elucidate the mechanism of epithelial differentiation and the function of Bmp signaling during prostatic development, conditional male mutant mouse analysis for the epithelial-specific Bmp receptor 1a (Bmpr1a) was performed. We demonstrate that Bmp signaling is indispensable for luminal cell maturation, which regulates basal cell proliferation. Expression of the prostatic epithelial regulatory gene Nkx3.1 was significantly reduced in the Bmpr1a mutants. These results indicate that Bmp signaling is a key factor for prostatic epithelial differentiation, possibly by controlling the prostatic regulatory gene Nkx3.1.

Indexed as

AnimalsBone Morphogenetic Protein Receptors, Type ICell DifferentiationCell Line, TumorCell ProliferationEpitheliumFemaleFluorescent Antibody TechniqueGene Expression Regulation, DevelopmentalHomeodomain ProteinsHumansHyperplasiaMaleMiceMice, Inbred C57BLMice, Inbred ICRBmpr1a protein, mouseBone Morphogenetic Protein Receptors, Type IHomeodomain ProteinsNkx3-1 protein, mouseReceptors, AndrogenSmad ProteinsTranscription Factors

Identifiers

PMID24731097
PMCPMC4060178
OpenAlexW1986703363

What OpenQuestion holds

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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.