Evidence map›Paper›PMID 23206285›Full record

ReviewNutrition reviews2012

Using components of the vitamin D pathway to prevent and treat colon cancer.

Renee E Stubbins, Aisha Hakeem, Nomelí P Núñez

Abstract readReview
In one paragraph

Review in Nutrition reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. EMT transcription factors: implication in osteosarcoma.Medical oncology (Northwood, London, England) · 2013
    Review
  12. Article
  13. 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

3 authors at 1 institution in 1 country.

Renee E StubbinsDepartment of Nutritional Sciences, University of Texas at Austin, Austin, Texas 78712, USA.
Aisha Hakeem
Nomelí P Núñez
The University of Texas at Austin · US

Funding

Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHEN, JIANJUN · 1996 to 2011
$16.4M
ENVIRONMENTAL TESTICULAR TOXICITY &GERM CELL APOPTOSISR01ES009145 · NIEHS · UNIVERSITY OF TEXAS AUSTIN · PI RICHBURG, JOHN H · 1997 to 2004
$1.5M
Beyond Adiposity: Insulin and Inflammation in Postmenopausal Breast CancerK22CA127519 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI NUNEZ, NOMELI PANIAGUA · 2007 to 2009
$575k
NCI NIH HHS 1K22CA127519-01A1NCI NIH HHS K22 CA127519NIEHS NIH HHS ES007784NIEHS NIH HHS ES09145NIEHS NIH HHS P30 ES007784NIEHS NIH HHS R01 ES009145
6 · The paper itself

Abstract

The objective of this review was to analyze the components of vitamin D and their potential usefulness in preventing and treating colorectal cancer. The active form of vitamin D, 1α,25(OH(2) )D(3) , targets the wnt/β-catenin pathway by upregulating key tumor suppressor genes such as E-cadherin, which promotes an epithelial phenotype, but this is only possible when the vitamin D receptor (VDR) is present. Colorectal cell lines have shown that VDR expression levels decrease in the later stages of colon cancer. In colorectal cancers with low VDR expression, treatments to increase VDR expression could target alterations at the genomic and epigenomic levels by modulating transcription factors such as SNAIL1 and by utilizing histone deacetyltransferase inhibitors, respectively. Finally, epidemiological studies suggest that the current US Recommended Dietary Allowance should be increased to 2,000 IU in order to raise serum 25(OH)D(3) levels above 30 ng/mL. This increase in vitamin D status can be obtained most efficiently from sun exposure or vitamin D supplementation. In summary, vitamin D and its metabolites could be utilized in strategies to treat and prevent colon cancer.

Indexed as

beta CateninCalcitriolCell Line, TumorColonic NeoplasmsDietDietary SupplementsHumansReceptors, CalcitriolTranscription FactorsWnt Proteinsbeta CateninCalcitriolReceptors, CalcitriolTranscription FactorsWnt Proteins

Identifiers

PMID23206285
PMCPMC3514827
OpenAlexW2056736968

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.