Evidence map›Paper›PMID 20554899›Full record

ArticleThe Journal of nutrition2010

Candidate dietary phytochemicals modulate expression of phase II enzymes GSTP1 and NQO1 in human lung cells.

Xiang-Lin Tan, Miao Shi, Hui Tang, Weiguo Han, Simon D Spivack

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 56 citations in OpenAlex.

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  18. High-throughput library screening identifies two novel NQO1 inducers in human lung cells.American journal of respiratory cell and molecular biology · 2012
    Article
  19. Article
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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

5 authors at 3 institutions in 1 country.

Xiang-Lin TanDivision of Pulmonary Medicine, Albert Einstein College of Medicine, Bronx, NY, USA. tan.xianglin@mayo.edu
Miao Shi
Hui Tang
Weiguo Han
Simon D Spivack
New York State Department of Health · USAlbert Einstein College of Medicine · USMayo Clinic in Florida · US

Funding

Mayo Cancer Genetic Epidemiology Training ProgramR25CA092049 · NCI · MAYO CLINIC ROCHESTER · PI PETERSEN, GLORIA M., VACHON, CELINE M · 2001 to 2018
$5.3M
Quantitative Gene Expression in Human Lung EpitheliumR01CA106186 · NCI · WADSWORTH CENTER · PI SPIVACK, SIMON D · 2003 to 2007
$1.8M
Carcinogen Metabolism Enzyme Expression in Buccal CellsR21CA094714 · NCI · WADSWORTH CENTER · PI SPIVACK, SIMON DANIEL · 2001 to 2003
$572k
NCI NIH HHS R01 CA 10618NCI NIH HHS R01 CA106186NCI NIH HHS R21 CA 94714NCI NIH HHS R25 CA092049
6 · The paper itself

Abstract

Many phytochemicals possess cancer-preventive properties, some putatively through phase II metabolism-mediated mutagen/oxidant quenching. We applied human lung cells in vitro to investigate the effects of several candidate phytopreventive agents, including green tea extracts (GTE), broccoli sprout extracts (BSE), epigallocatechin gallate (EGCG), sulforaphane (SFN), phenethyl isothiocyanate (PEITC), and benzyl isothiocyanate (BITC), on inducing phase II enzymes glutathione S-transferase P1 (GSTP1) and NAD(P)H:quinone oxidoreductase 1 (NQO1) at mRNA and protein levels. Primary normal human bronchial epithelial cells (NHBE), immortalized human bronchial epithelial cells (HBEC), and lung adenocarcinoma cells (A549) were exposed to diet-achievable levels of GTE and BSE (0.5, 1.0, 2.0 mg/L), or individual index components EGCG, SFN, PEITC, BITC (0.5, 1.0, 2.0 micromol/L) for 24 h, 48 h, and 6 d, respectively. mRNA assays employed RNA-specific quantitative RT-PCR and protein assays employed Western blotting. We found that in NHBE cells, while GSTP1 mRNA levels were slightly but significantly increased after exposure to GTE or BSE, NQO1 mRNA increased to 2- to 4-fold that of control when exposed to GTE, BSE, or SFN. Effects on NQO1 mRNA expression in HBEC cells were similar. NQO1 protein expression increased up to 11.8-fold in SFN-treated NHBE cells. Both GSTP1 and NQO1 protein expression in A549 cells were constitutively high but not induced under any condition. Our results suggest that NQO1 is more responsive to the studied chemopreventive agents than GSTP1 in human lung cells and there is discordance between single agent and complex mixture effects. We conclude that modulation of lung cell phase II metabolism by chemopreventive agents requires cell- and agent-specific discovery and testing.

Indexed as

Anticarcinogenic AgentsBrassicaBronchiCamellia sinensisCatechinCell DivisionCell LineCell Line, TumorEpithelial CellsGene ExpressionGlutathione S-Transferase piHumansIsothiocyanatesLungLung NeoplasmsNAD(P)H Dehydrogenase (Quinone)Anticarcinogenic Agentsbenzyl isothiocyanateCatechinepigallocatechin gallateGlutathione S-Transferase piGSTP1 protein, humanIsothiocyanatesNAD(P)H Dehydrogenase (Quinone)NQO1 protein, humanphenethyl isothiocyanatePlant ExtractsRNA, MessengersulforaphaneSulfoxidesThiocyanates

Identifiers

PMID20554899
PMCPMC2903300
OpenAlexW2171905533

What OpenQuestion holds

Textmetadata
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.