Evidence map›Paper›PMID 24909172›Full record

ArticleOncogene2015

Mammary glands exhibit molecular laterality and undergo left-right asymmetric ductal epithelial growth in MMTV-cNeu mice.

J P Robichaux, R M Hallett, J W Fuseler, J A Hassell, A F Ramsdell

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. From cytoskeletal dynamics to organ asymmetry: a nonlinear, regulative pathway underlies left-right patterning.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  11. Left-right analysis of mammary gland development in retinoid X receptor-α+/- mice.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Article
  12. Article
  13. Article
  14. In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci.Mammalian genome : official journal of the International Mammalian Genome Society · 2015
    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 3 institutions in 2 countries.

J P RobichauxDepartment of Regenerative Medicine and Cell Biology and Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
R M HallettDepartment of Biochemistry and Biomedical Sciences, Centre for Functional Genomics, McMaster University, Hamilton, ON, Canada.
J W FuselerDepartment of Cell Biology and Anatomy, School of Medicine, University of South Carolina, Columbia, SC, USA.
J A HassellDepartment of Biochemistry and Biomedical Sciences, Centre for Functional Genomics, McMaster University, Hamilton, ON, Canada.
A F Ramsdell1] Department of Regenerative Medicine and Cell Biology and Hollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA [2] Department of Cell Biology and Anatomy, School of Medicine, University of South Carolina, Columbia, SC, USA [3] Program In Women's and Gender Studies, College of Arts and Sciences, University of South Carolina, Columbia, SC, USA.
McMaster University · CAUniversity of South Carolina · USMedical University of South Carolina · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
Development of Xenopus as a Model to Study Congenital Heart DiseaseK02HL086737 · NHLBI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI RAMSDELL, ANN F · 2007 to 2011
$520k
Mammary Gland Laterality in Normal and Neoplastic DevelopmentR21HD068993 · NICHD · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI RAMSDELL, ANN F, SPYROPOULOS, DEMETRI D · 2011 to 2012
$411k
NCI NIH HHS P30 CA138313NCI NIH HHS P30CA138313NHLBI NIH HHS K02 HL086737NHLBI NIH HHS K02HL086737NICHD NIH HHS R21 HD068993NICHD NIH HHS R21HD068993
6 · The paper itself

Abstract

Significant left-right (L-R) differences in tumor incidence and disease outcome occur for cancers of paired organs, including the breasts; however, the basis for this laterality is unknown. Here, we show that despite their morphologic symmetry, left versus right mammary glands in wild-type mice have baseline differences in gene expression that are L-R independently regulated during pubertal development, including genes that regulate luminal progenitor cell renewal, luminal cell differentiation, mammary tumorigenesis, tamoxifen sensitivity and chemotherapeutic resistance. In MMTV-cNeu(Tg/Tg) mice, which model HER2/Neu-amplified breast cancer, baseline L-R differences in mammary gene expression are amplified, sustained or inverted in a gene-specific manner and the mammary ductal epithelium undergoes L-R asymmetric growth and patterning. Comparative genomic analysis of mouse L-R mammary gene expression profiles with gene expression profiles of human breast tumors revealed significant linkage between right-sided gene expression and decreased breast cancer patient survival. Collectively, these findings are the first to demonstrate that mammary glands are lateralized organs, and, moreover, that mammary glands have L-R differential susceptibility to HER2/Neu oncogene-mediated effects on ductal epithelial growth and differentiation. We propose that intrinsic molecular laterality may have a role in L-R asymmetric breast tumor incidence and, furthermore, that interplay between the L-R molecular landscape and oncogene activity may contribute to the differential disease progression and patient outcome that are associated with tumor situs.

Indexed as

AnimalsBreast NeoplasmsCell Transformation, NeoplasticFemaleGene ExpressionHumansMammary Glands, AnimalMammary Glands, HumanMammary Neoplasms, ExperimentalMiceSignal Transduction

Identifiers

PMID24909172
PMCPMC4261057
OpenAlexW2159912899

What OpenQuestion holds

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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.