Evidence map›Paper›PMID 25236912›Full record

ReviewCancer letters2014

Epigenetic regulation by selected dietary phytochemicals in cancer chemoprevention.

Samriddhi Shukla, Syed M Meeran, Santosh K Katiyar

Open access · greenAbstract readReview
In one paragraph

Review in Cancer letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.4field-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

49 citing papers in PubMed, 130 citations in OpenAlex.

  1. Review
  2. Article
  3. Curcumin in High Doses Reverses the UV-B-InducedPharmaceuticals (Basel, Switzerland) · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Frontiers in pharmacology · 2021
    Article
  17. Review
  18. Review
  19. Ayurveda and Epigenetics.Medicina (Kaunas, Lithuania) · 2020
    Review
  20. 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

3 authors at 2 institutions in 2 countries.

Samriddhi ShuklaCancer Epigenetic Laboratory, Division of Endocrinology, CSIR-Central Drug Research Institute, Lucknow 226021, India.
Syed M MeeranCancer Epigenetic Laboratory, Division of Endocrinology, CSIR-Central Drug Research Institute, Lucknow 226021, India.
Santosh K KatiyarDepartment of Dermatology, University of Alabama, Birmingham, AL 35294, USA; Comprehensive Cancer Center, University of Alabama, Birmingham, AL 35294, USA; Birmingham Veterans Affairs Medical Center, Birmingham, AL 35233, USA. Electronic address: skatiyar@uab.edu.
Central Drug Research Institute · INUniversity of Alabama at Birmingham · US

Funding

Prevention of UV-carcinogenesis through DNA repair-dependent immunomodulationR01CA140197 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KATIYAR, SANTOSH KUMAR, XU, HUI · 2010 to 2014
$1.4M
Epigenetic modulation by green tea in prevention of photocarcinogenesisR21CA140832 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KATIYAR, SANTOSH KUMAR · 2010 to 2011
$346k
Prevention of photocarcinogenesis by dietary immunomodulationI01BX001410 · VA · BIRMINGHAM VA MEDICAL CENTER · PI KATIYAR, SANTOSH KUMAR · 2012 to 2015
–
BLRD VA I01 BX001410NCI NIH HHS CA140197NCI NIH HHS CA140832NCI NIH HHS R01 CA140197NCI NIH HHS R21 CA140832
6 · The paper itself

Abstract

The growing interest in cancer epigenetics is largely due to the reversible nature of epigenetic changes which tend to alter during the course of carcinogenesis. Major epigenetic changes including DNA methylation, chromatin modifications and miRNA regulation play important roles in tumorigenic process. There are several epigenetically active synthetic molecules such as DNA methyltransferase (DNMTs) and histone deacetylases (HDACs) inhibitors, which are either approved or, are under clinical trials for the treatment of various cancers. However, most of the synthetic inhibitors have shown adverse side effects, narrow in their specificity and also expensive. Hence, bioactive phytochemicals, which are widely available with lesser toxic effects, have been tested for their role in epigenetic modulatory activities in gene regulation for cancer prevention and therapy. Encouragingly, many bioactive phytochemicals potentially altered the expression of key tumor suppressor genes, tumor promoter genes and oncogenes through modulation of DNA methylation and chromatin modification in cancer. These bioactive phytochemicals either alone or in combination with other phytochemicals showed promising results against various cancers. Here, we summarize and discuss the role of some commonly investigated phytochemicals and their epigenetic targets that are of particular interest in cancer prevention and cancer therapy.

Indexed as

AcetylationAnimalsAnticarcinogenic AgentsAntineoplastic Agents, PhytogenicChromatin Assembly and DisassemblyDNA MethylationEpigenesis, GeneticGene Expression Regulation, NeoplasticHistonesHumansNeoplasmsPhytochemicalsAnticarcinogenic AgentsAntineoplastic Agents, PhytogenicHistonesPhytochemicalsCancerDNA methylationEpigeneticsHistone deacetylationPhytochemicals

Identifiers

PMID25236912
PMCPMC4197101
OpenAlexW2167637569

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.