Evidence map›Paper›PMID 23457599›Full record

ArticlePloS one2013

Gpr177 deficiency impairs mammary development and prohibits Wnt-induced tumorigenesis.

Eri Ohfuchi Maruyama, H-M Ivy Yu, Ming Jiang, Jiang Fu, Wei Hsu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. The requirement of SUMO2/3 for SENP2 mediated extraembryonic and embryonic development.Developmental dynamics : an official publication of the American Association of Anatomists · 2020
    Article
  4. Article
  5. Rap1b Is an Effector of Axin2 Regulating Crosstalk of Signaling Pathways During Skeletal Development.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  6. Ectodermal Wnt controls nasal pit morphogenesis through modulation of the BMP/FGF/JNK signaling axis.Developmental dynamics : an official publication of the American Association of Anatomists · 2016
    Article
  7. Article
  8. Article
  9. Wls promotes the proliferation of breast cancer cells via Wnt signaling.Medical oncology (Northwood, London, England) · 2015
    Article
  10. Article
  11. 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

5 authors at 1 institution in 1 country.

Eri Ohfuchi MaruyamaDepartment of Biomedical Genetics, University of Rochester Medical Center, Rochester, New York, United States of America.
H-M Ivy Yu
Ming Jiang
Jiang Fu
Wei Hsu
University of Rochester Medical Center · US

Funding

GENETIC REGULATORY NETWORK IN CRANIOFACIAL DEVELOPMENTR01DE015654 · NIDCR · UNIVERSITY OF ROCHESTER · PI Wei Hsu · 2006 to 2026
$8.2M
Genetic Regulatory Network in Mammary TumorigenesisR01CA106308 · NCI · UNIVERSITY OF ROCHESTER · PI HSU, WEI · 2004 to 2014
$3.1M
NCI NIH HHS CA106308NCI NIH HHS R01 CA106308NIDCR NIH HHS R01 DE015654
6 · The paper itself

Abstract

Aberrant regulation of the Wnt pathway, essential for various developmental processes, is tightly linked to human breast cancers. By hijacking this evolutionary conserved signaling pathway, cancer cells acquire sustaining proliferation ability, leading to modification of physiologic properties necessary for tumor initiation and progression. An enormous wealth of knowledge on the importance of Wnt signaling in breast development and cancer has been obtained, but the cell types responsible for production of this proliferative signal operating within normal and malignant tissues remains poorly understood. Here we report that Wnt production mediated by Gpr177 is essential for mammary morphogenesis. The loss of Gpr177 interferes with mammary stem cells, leading to deficiencies in cell proliferation and differentiation. Genetic analysis further demonstrates an indispensable role of Gpr177 in Wnt-induced tumorigenesis. The Gpr177-deficiency mice are resistant to malignant transformation. This study not only demonstrates the necessity of Wnt in mammary organogenesis but also provides a proof-of-principle for targeting of Gpr177 as a potential new treatment for human diseases with aberrant Wnt stimulation.

Indexed as

AnimalsCell DifferentiationCell LineCell ProliferationFemaleHyperplasiaIntracellular Signaling Peptides and ProteinsMammary Glands, AnimalMammary Neoplasms, ExperimentalMiceMorphogenesisReceptors, G-Protein-CoupledSignal TransductionStem CellsWnt ProteinsGpr177 protein, mouseIntracellular Signaling Peptides and ProteinsReceptors, G-Protein-CoupledWnt Proteins

Identifiers

PMID23457599
PMCPMC3574013
OpenAlexW2017530259

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.