Evidence map›Paper›PMID 21882252›Full record

ArticleMolecular carcinogenesis2012

Green tea catechin extract in intervention of chronic breast cell carcinogenesis induced by environmental carcinogens.

Kusum Rathore, Hwa-Chain Robert Wang

Abstract read
In one paragraph

Article in Molecular carcinogenesis, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Therapeutic properties of green tea against environmental insults.The Journal of nutritional biochemistry · 2017
    Review
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Protective mechanisms of green tea polyphenols in skin.Oxidative medicine and cellular longevity · 2012
    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

2 authors at 1 institution in 1 country.

Kusum RathoreDepartment of Biomedical and Diagnostic Sciences, College of Veterinary Medicine, The University of Tennessee, Knoxville, Tennessee 37996, USA.
Hwa-Chain Robert Wang
University of Tennessee at Knoxville · US

Funding

Role of COX-2 in UVB-induced beta-catenin signaling in keratinocytesR21AR057579 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PELLING, JILL C. · 2010 to 2011
$386k
Green tea catechins in precancerorus preventionR21CA129772 · NCI · UNIVERSITY OF TENNESSEE KNOXVILLE · PI WANG, HWA-CHAIN ROBERT · 2008 to 2009
$353k
Carcinogenesis cellular model for identifying preventive agentsR03CA125795 · NCI · UNIVERSITY OF TENNESSEE KNOXVILLE · PI WANG, HWA-CHAIN ROBERT · 2007 to 2008
$145k
NCI NIH HHS CA129772NCI NIH HHS R03 CA125795NCI NIH HHS R21 CA129772NIAMS NIH HHS AR057579
6 · The paper itself

Abstract

Sporadic breast cancers are mainly attributable to long-term exposure to environmental factors, via a multi-year, multi-step, and multi-path process of tumorigenesis involving cumulative genetic and epigenetic alterations in the chronic carcinogenesis of breast cells from a non-cancerous stage to precancerous and cancerous stages. Epidemiologic and experimental studies have suggested that green tea components may be used as preventive agents for breast cancer control. In our research, we have developed a cellular model that mimics breast cell carcinogenesis chronically induced by cumulative exposures to low doses of environmental carcinogens. In this study, we used our chronic carcinogenesis model as a target system to investigate the activity of green tea catechin extract (GTC) at non-cytotoxic levels in intervention of cellular carcinogenesis induced by cumulative exposures to pico-molar 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and benzo[a]pyrene (B[a]P). We identified that GTC, at a non-cytotoxic, physiologically achievable concentration of 2.5 µg/mL, was effective in suppressing NNK- and B[a]P-induced cellular carcinogenesis, as measured by reduction of the acquired cancer-associated properties of reduced dependence on growth factors, anchorage-independent growth, increased cell mobility, and acinar-conformational disruption. We also detected that intervention of carcinogen-induced elevation of reactive oxygen species (ROS), increase of cell proliferation, activation of the ERK pathway, DNA damage, and changes in gene expression may account for the mechanisms of GTC's preventive activity. Thus, GTC may be used in dietary and chemoprevention of breast cell carcinogenesis associated with long-term exposure to low doses of environmental carcinogens.

Indexed as

Benzo(a)pyreneBreastBreast NeoplasmsCarcinogens, EnvironmentalCatechinCell LineCell ProliferationCell Transformation, NeoplasticFemaleGene Expression RegulationHistonesHumansNitrosaminesPhosphorylationPlant ExtractsReactive Oxygen Species4-(N-methyl-N-nitrosamino)-1-(3-pyridyl)-1-butanoneBenzo(a)pyreneCarcinogens, EnvironmentalCatechinHistonesNitrosaminesPlant ExtractsReactive Oxygen SpeciesTea

Identifiers

PMID21882252
PMCPMC3229645
OpenAlexW2037315640

What OpenQuestion holds

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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.