Evidence map›Paper›PMID 21254334›Full record

ArticleGenesis (New York, N.Y. : 2000)2011

Forced involution of the functionally differentiated mammary gland by overexpression of the pro-apoptotic protein bax.

Edmund B Rucker, Amber N Hale, David C Durtschi, Kazuhito Sakamoto, Kay-Uwe Wagner

Abstract read
In one paragraph

Article in Genesis (New York, N.Y. : 2000), 2011. 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
2.0field-weighted citation impact, top 15% 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, 19 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Edmund B RuckerBiology Department, University of Kentucky, Lexington, Kentucky, USA. Edmund.rucker@uky.edu
Amber N Hale
David C Durtschi
Kazuhito Sakamoto
Kay-Uwe Wagner
University of Kentucky · USUniversity of Nebraska Medical Center · USUniversity of Tennessee at Knoxville · US

Funding

Growth-Regulatory Signaling Networks in Breast CancerR01CA117930 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WAGNER, KAY-UWE · 2006 to 2016
$2.5M
NCI NIH HHS CA117930NCI NIH HHS R01 CA117930
6 · The paper itself

Abstract

The mammary gland is a developmentally dynamic, hormone-responsive organ that undergoes proliferation and differentiation within the secretory epithelial compartment during pregnancy. The epithelia are maintained by pro-survival signals (e.g., Stat5, Akt1) during lactation, but undergo apoptosis during involution through inactivation of cell survival pathways and upregulation of pro-apoptotic proteins. To assess if the survival signals in the functionally differentiated mammary epithelial cells can override a pro-apoptotic signal, we generated transgenic mice that express Bax under the whey acidic protein (WAP) promoter. WAP-Bax females exhibited a lactation defect and were unable to nourish their offspring. Mammary glands demonstrated: (1) a reduction in epithelial content, (2) hallmark signs of mitochondria-mediated cell death, (3) an increase in apoptotic cells by TUNEL assay, and (4) precocious Stat3 activation. This suggests that upregulation of a single pro-apoptotic factor of the Bcl-2 family is sufficient to initiate apoptosis of functionally differentiated mammary epithelial cells in vivo.

Indexed as

ApoptosisAnimalsbcl-2-Associated X ProteinCell DifferentiationEpithelial CellsFemaleGenetic VectorsImmunohistochemistryLactationMammary Glands, AnimalMiceMice, TransgenicMilk ProteinsPromoter Regions, GeneticProto-Oncogene Proteins c-aktSTAT5 Transcription FactorAkt1 protein, mousebcl-2-Associated X ProteinMilk ProteinsProto-Oncogene Proteins c-aktSTAT5 Transcription Factorwhey acidic proteins

Identifiers

PMID21254334
PMCPMC3703757
OpenAlexW2103437629

What OpenQuestion holds

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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.