Evidence map›Paper›PMID 27808166›Full record

ArticleScientific reports2016

LPA receptor activity is basal specific and coincident with early pregnancy and involution during mammary gland postnatal development.

Deanna Acosta, Susmita Bagchi, Pilib Ó Broin, Daniel Hollern, Silvia E Racedo, Bernice Morrow, Rani S Sellers, John M Greally, Aaron Golden, Eran Andrechek and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. In silico mapping of quantitative trait loci (QTL) regulating the milk ionome in mice identifies a milk iron locus on chromosome 1.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Article
  5. Article
  6. 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

12 authors at 3 institutions in 1 country.

Deanna AcostaDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Susmita BagchiDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Pilib Ó BroinDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Daniel HollernDepartment of Physiology, Michigan State University, East Lansing, MI, 48824, USA.
Silvia E RacedoDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Bernice MorrowDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Rani S SellersDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
John M GreallyDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Aaron GoldenDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Eran AndrechekDepartment of Physiology, Michigan State University, East Lansing, MI, 48824, USA.
Teresa WoodDepartment of Neurology and Neuroscience, Rutgers New Jersey Medical School, Newark, NJ, 07101, USA.
Cristina MontagnaDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Albert Einstein College of Medicine · USMichigan State University · USRutgers, The State University of New Jersey · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Training in Aging ResearchT32AG023475 · NIA · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI NIR J BARZILAI, DEREK Major HUFFMAN · 2004 to 2026
$8.6M
NCI NIH HHS P30 CA013330NIA NIH HHS T32 AG023475NIDDK NIH HHS P30 DK020541
6 · The paper itself

Abstract

During pregnancy, luminal and basal epithelial cells of the adult mammary gland proliferate and differentiate resulting in remodeling of the adult gland. While pathways that control this process have been characterized in the gland as a whole, the contribution of specific cell subtypes, in particular the basal compartment, remains largely unknown. Basal cells provide structural and contractile support, however they also orchestrate the communication between the stroma and the luminal compartment at all developmental stages. Using RNA-seq, we show that basal cells are extraordinarily transcriptionally dynamic throughout pregnancy when compared to luminal cells. We identified gene expression changes that define specific basal functions acquired during development that led to the identification of novel markers. Enrichment analysis of gene sets from 24 mouse models for breast cancer pinpoint to a potential new function for insulin-like growth factor 1 (Igf1r) in the basal epithelium during lactogenesis. We establish that β-catenin signaling is activated in basal cells during early pregnancy, and demonstrate that this activity is mediated by lysophosphatidic acid receptor 3 (Lpar3). These findings identify novel pathways active during functional maturation of the adult mammary gland.

Indexed as

Animalsbeta CateninCell LineageEpithelial CellsFemaleGene Expression ProfilingInsulin-Like Growth Factor ILactationMammary Glands, AnimalMiceOrganogenesisPregnancybeta Catenininsulin-like growth factor-1, mouseInsulin-Like Growth Factor I

Identifiers

PMID27808166
PMCPMC5093903
OpenAlexW2546534149

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.