Evidence map›Paper›PMID 25088245›Full record

ArticleReproductive toxicology (Elmsford, N.Y.)2015

Paradoxical zinc toxicity and oxidative stress in the mammary gland during marginal dietary zinc deficiency.

Zeynep Bostanci, Ronald P Mack, Sooyeon Lee, David I Soybel, Shannon L Kelleher

Abstract read
In one paragraph

Article in Reproductive toxicology (Elmsford, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Zinc and Oxidative Stress: Current Mechanisms.Antioxidants (Basel, Switzerland) · 2017
    Review
  8. Zinc transporters and dysregulated channels in cancers.Frontiers in bioscience (Landmark edition) · 2017
    Review
  9. Article
  10. Review
  11. Article
  12. 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 2 institutions in 1 country.

Zeynep BostanciDepartment of Nutritional Sciences, The Pennsylvania State University, United States; Department of Surgery, Penn State Hershey College of Medicine, United States.
Ronald P MackDepartment of Nutritional Sciences, The Pennsylvania State University, United States; Department of Kinesiology, The Pennsylvania State University, United States.
Sooyeon LeeDepartment of Nutritional Sciences, The Pennsylvania State University, United States; Interdisciplinary Graduate Program in Physiology, The Pennsylvania State University, United States.
David I SoybelDepartment of Nutritional Sciences, The Pennsylvania State University, United States; Department of Surgery, Penn State Hershey College of Medicine, United States; Department of Cell and Molecular Physiology, Penn State Hershey College of Medicine, United States.
Shannon L KelleherDepartment of Nutritional Sciences, The Pennsylvania State University, United States; Interdisciplinary Graduate Program in Physiology, The Pennsylvania State University, United States; Department of Surgery, Penn State Hershey College of Medicine, United States; Department of Cell and Molecular Physiology, Penn State Hershey College of Medicine, United States. Electronic address: slk39@psu.edu.
Penn State Milton S. Hershey Medical Center · USPennsylvania State University · US

Funding

Regulation of Cellular Zn Redistribution: A Role of ZnT2R01HD058614 · NICHD · PENNSYLVANIA STATE UNIVERSITY, THE · PI KELLEHER, SHANNON L · 2008 to 2012
$1.4M
NICHD NIH HHS R01 HD058614PHS HHS NIH 058614
6 · The paper itself

Abstract

Zinc (Zn) regulates numerous cellular functions. Zn deficiency is common in females; ∼80% of women and 40% of adolescent girls consume inadequate Zn. Zn deficiency enhances oxidative stress, inflammation and DNA damage. Oxidative stress and inflammation is associated with breast disease. We hypothesized that Zn deficiency increases oxidative stress in the mammary gland, altering the microenvironment and architecture. Zn accumulated in the mammary glands of Zn deficient mice and this was associated with macrophage infiltration, enhanced oxidative stress and over-expression of estrogen receptor α. Ductal and stromal hypercellularity was associated with aberrant collagen deposition and disorganized e-cadherin. Importantly, these microenvironmental alterations were associated with substantial impairments in ductal expansion and mammary gland development. This is the first study to show that marginal Zn deficiency creates a toxic microenvironment in the mammary gland impairing breast development. These changes are consistent with hallmarks of potential increased risk for breast disease and cancer.

Indexed as

DietOxidative StressAge FactorsAnimalsCation Transport ProteinsCell ProliferationCellular MicroenvironmentCollagenDeficiency DiseasesDisease Models, AnimalEstrogen Receptor alphaFemaleHumansHyperplasiaMacrophagesMammary Glands, AnimalCation Transport ProteinsCollagenEstrogen Receptor alphaZincBreast cancerCollagenDuctal hyperplasiaEstrogen receptorMammary glandOxidative stressZinc transporter

Identifiers

PMID25088245
PMCPMC4312747
OpenAlexW2048702154

What OpenQuestion holds

Textmetadata
LicenceTDM
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.