Evidence map›Paper›PMID 28579119›Full record

ReviewMolecular and cellular endocrinology2017

Function of the vitamin D endocrine system in mammary gland and breast cancer.

JoEllen Welsh

Open access · greenAbstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Association of Vitamin D Intake,Medical sciences (Basel, Switzerland) · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Vitamin DScientific reports · 2024
    Article
  10. Article
  11. Micronutrient Status and Breast Cancer: A Narrative Review.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Carbohydrate content of human milk is affected by seasonal variations: a retrospective observational study.Journal of perinatology : official journal of the California Perinatal Association · 2022
    Observational
  18. Review
  19. Vitamin D regulation of energy metabolism in cancer.British journal of pharmacology · 2022
    Review
  20. The TSH/Thyroid Hormones Axis and Breast Cancer.Journal of clinical medicine · 2022
    Review
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

1 author at 1 institution in 1 country.

JoEllen WelshUniversity at Albany Cancer Research Center, 1 Discovery Drive, Rensselaer, NY 12144, United States. Electronic address: jwelsh@albany.edu.
University at Albany, State University of New York · US

Funding

VITAMIN D MEDICATED APOPTOSIS IN MAMMARY CELLSR01CA069700 · NCI · UNIVERSITY OF NOTRE DAME · PI WELSH, JOELLEN · 1995 to 2009
$2.8M
Vitamin D and HA Signaling in TNBCR01CA194500 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI WELSH, JOELLEN · 2015 to 2019
$2.2M
Bioassay for Breast Cancer PreventionRC1CA144963 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI WELSH, JOELLEN · 2009 to 2010
$996k
Vitamin D, Metabolic Flux and Breast CancerR21CA166434 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI WELSH, JOELLEN · 2013 to 2014
$354k
NCI NIH HHS R01 CA069700NCI NIH HHS R01 CA194500NCI NIH HHS R21 CA166434NCI NIH HHS RC1 CA144963
6 · The paper itself

Abstract

The nuclear receptor for 1α,25-dihydroxycholecalciferol (1,25D), the active form of vitamin D, has anti-tumor actions in many tissues. The vitamin D receptor (VDR) is expressed in normal mammary gland and in many human breast cancers suggesting it may represent an important tumor suppressor gene in this tissue. When activated by 1,25D, VDR modulates multiple cellular pathways including those related to energy metabolism, terminal differentiation and inflammation. There is compelling pre-clinical evidence that alterations in vitamin D status affect breast cancer development and progression, while clinical and epidemiological data are suggestive but not entirely consistent. The demonstration that breast cells express CYP27B1 (which converts the precursor vitamin D metabolite 25D to the active metabolite 1,25D) and CYP24A1 (which degrades both 25D and 1,25D) provides insight into the difficulties inherent in using dietary vitamin D, sun exposure and/or serum biomarkers of vitamin D status to predict disease outcomes. Emerging evidence suggests that the normally tight balance between CYP27B1 and CYP24A1 becomes deregulated during cancer development, leading to abrogation of the tumor suppressive effects triggered by VDR. Research aimed at understanding the mechanisms that govern uptake, storage, metabolism and actions of vitamin D steroids in normal and neoplastic breast tissue remain an urgent priority.

Indexed as

25-Hydroxyvitamin D3 1-alpha-HydroxylaseAnimalsBreast NeoplasmsDisease Models, AnimalDisease ProgressionFemaleHumansMammary Glands, HumanMiceReceptors, CalcitriolVitamin DVitamin D3 24-Hydroxylase25-Hydroxyvitamin D3 1-alpha-HydroxylaseCYP24A1 protein, humanCYP27B1 protein, humanReceptors, CalcitriolVDR protein, humanVitamin DVitamin D3 24-HydroxylaseBreast cancerCYP24A1CYP27B1Mammary glandMetabolismVDRVitamin D

Identifiers

PMID28579119
PMCPMC5538720
OpenAlexW2621053491

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.