Evidence map›Paper›PMID 27552186›Full record

ArticleNutrition and cancer2016

1α,25-Dihydroxyvitamin D Inhibits the Metastatic Capability of MCF10CA1a and MDA-MB-231 Cells in an In Vitro Model of Breast to Bone Metastasis.

Tomasz Wilmanski, Alle Barnard, Mukti R Parikh, Julia Kirshner, Kimberly Buhman, John Burgess, Dorothy Teegarden

Abstract read
In one paragraph

Article in Nutrition and cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  11. Vitamin D as a Potential Preventive Agent For Young Women's Breast Cancer.Cancer prevention research (Philadelphia, Pa.) · 2021
    Review
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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

7 authors.

Tomasz Wilmanskia Department of Nutrition Science, Interdepartmental Nutrition Program , Purdue University , West Lafayette , Indiana , USA.
Alle Barnarda Department of Nutrition Science, Interdepartmental Nutrition Program , Purdue University , West Lafayette , Indiana , USA.
Mukti R Parikhb Interdisciplinary Life Science-PULSe , Purdue University , West Lafayette , Indiana , USA.
Julia Kirshnerc Department of Biological Sciences , Purdue University , West Lafayette , Indiana , USA.
Kimberly Buhmana Department of Nutrition Science, Interdepartmental Nutrition Program , Purdue University , West Lafayette , Indiana , USA.
John Burgessa Department of Nutrition Science, Interdepartmental Nutrition Program , Purdue University , West Lafayette , Indiana , USA.
Dorothy Teegardena Department of Nutrition Science, Interdepartmental Nutrition Program , Purdue University , West Lafayette , Indiana , USA.

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Interdisciplinary Cancer Prevention Research Internship ProgramR25CA128770 · NCI · PURDUE UNIVERSITY · PI TEEGARDEN, DOROTHY · 2008 to 2012
$1.5M
NCATS NIH HHS UL1 TR001108NCI NIH HHS P30 CA023168NCI NIH HHS R25 CA128770
6 · The paper itself

Abstract

Breast cancer metastasis to the bone continues to be a major health problem, with approximately 80% of advanced breast cancer patients expected to develop bone metastasis. Although the problem of bone metastasis persists, current treatment options for metastatic cancer patients are limited. In this study, we investigated the preventive role of the active vitamin D metabolite, 1α,25-dihydroxyvitamin D (1,25(OH)2D), against the metastatic potential of breast cancer cells using a novel three-dimensional model (rMET) recapitulating multiple steps of the bone metastatic process. Treatment of MCF10CA1a and MDA-MB-231 cells inhibited metastasis in the rMET model by 70% (±5.7%) and 21% (±6%), respectively. In addition, 1,25(OH)2D treatment decreased invasiveness (20 ± 11% of vehicle) and decreased the capability of MCF10CA1a cells to survive in the reconstructed bone environment after successful invasion through the basement membrane (69 ± 5% of vehicle). An essential step in metastasis is epithelial-mesenchymal transition (EMT). Treatment of MCF10CA1a cells with 1,25(OH)2D increased gene (2.04 ± 0.28-fold increase) and protein (1.87 ± 0.20-fold increase) expression of E-cadherin. Additionally, 1,25(OH)2D treatment decreased N-cadherin gene expression (42 ± 8% decrease), a marker for EMT. Collectively, the present study suggests that 1,25(OH)2D inhibits breast cancer cell metastatic capability as well as inhibits EMT, an essential step in the metastatic process.

Indexed as

Epithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticAnticarcinogenic AgentsAntigens, CDBiomarkers, TumorBone NeoplasmsBreastBreast NeoplasmsCadherinsCell LineCell Line, TumorCell ProliferationCell SurvivalFemaleHumansKinetics1,25-dihydroxyvitamin DAnticarcinogenic AgentsAntigens, CDBiomarkers, TumorCadherinsCDH1 protein, humanCDH2 protein, humanNeoplasm ProteinsVitamin D

Identifiers

PMID27552186
PMCPMC5047026

What OpenQuestion holds

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Registered trials

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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.