Evidence map›Paper›PMID 28096336›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

β-Catenin haploinsufficiency promotes mammary tumorigenesis in an ErbB2-positive basal breast cancer model.

Tung Bui, Babette Schade, Robert D Cardiff, Olulanu H Aina, Virginie Sanguin-Gendreau, William J Muller

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Tung BuiGoodman Cancer Center, McGill University, Montreal, QC H3A 1A3, Canada.
Babette SchadeGoodman Cancer Center, McGill University, Montreal, QC H3A 1A3, Canada.
Robert D CardiffCenter for Comparative Medicine, University of California, Davis, CA 95616.
Olulanu H AinaCenter for Comparative Medicine, University of California, Davis, CA 95616.
Virginie Sanguin-GendreauGoodman Cancer Center, McGill University, Montreal, QC H3A 1A3, Canada.
William J MullerGoodman Cancer Center, McGill University, Montreal, QC H3A 1A3, Canada; william.muller@mcgill.ca.
McGill University · CAUniversity of California, Davis · US

Funding

The Center for Translational Genomic PhenotypingU01CA141582 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARDIFF, ROBERT D, CHERRY, SIMON R · 2009 to 2013
$3.5M
NCI NIH HHS U01 CA141582
6 · The paper itself

Abstract

Aberrant activation of β-catenin through its activity as a transcription factor has been observed in a large proportion of human malignancies. Despite the improved understanding of the β-catenin signaling pathway over the past three decades, attempts to develop therapies targeting β-catenin remain challenging, and none of these targeted therapies have advanced to the clinic. In this study, we show that part of the challenge in antagonizing β-catenin is caused by its dual functionality as a cell adhesion molecule and a signaling molecule. In a mouse model of basal ErbB2 receptor tyrosine kinase 2 (ErbB2)-positive breast cancer (ErbB2

Indexed as

Animalsbeta CateninEpithelial-Mesenchymal TransitionErb-b2 Receptor Tyrosine KinasesFemalegamma CateninHaploinsufficiencyLung NeoplasmsMammary Neoplasms, ExperimentalMice, TransgenicRNA, Small InterferingSignal TransductionTumor Cells, Culturedbeta CateninCTNNB1 protein, mouseErbb2 protein, mouseErb-b2 Receptor Tyrosine Kinasesgamma CateninJup protein, mouseRNA, Small Interferingbeta-cateninbreast cancercell junctionErbB2transgenic model

Identifiers

PMID28096336
PMCPMC5293039
OpenAlexW2574116680

What OpenQuestion holds

Textmetadata
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.