Evidence map›Paper›PMID 18586690›Full record

ArticleCarcinogenesis2008

Differential effects of resveratrol on androgen-responsive LNCaP human prostate cancer cells in vitro and in vivo.

Thomas T Y Wang, Tamaro S Hudson, Tien-Chung Wang, Connie M Remsberg, Neal M Davies, Yoko Takahashi, Young S Kim, Harold Seifried, Bryan T Vinyard, Susan N Perkins and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
6.1field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 117 citations in OpenAlex.

  1. Dietary polyphenols in prevention and treatment of prostate cancer.International journal of molecular sciences · 2015
    Pooled it
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  17. Leelamine suppresses cMyc expression in prostate cancer cellsJournal of cancer metastasis and treatment · 2021
    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

11 authors at 8 institutions in 2 countries.

Thomas T Y WangDiet, Genomics and Immunology Laboratory, Beltsville Human Nutrition Research Center, United States Department of Agriculture, 10300 Baltimore Avenue, Beltsville, MD 20705, USA. tom.wang@ars.usda.gov
Tamaro S Hudson
Tien-Chung Wang
Connie M Remsberg
Neal M Davies
Yoko Takahashi
Young S Kim
Harold Seifried
Bryan T Vinyard
Susan N Perkins
Stephen D Hursting
National Institutes of Health · USUnited States Department of Agriculture · USWashington State University · USFood Research Institute · JPNational Cancer Institute · USThe University of Texas at Austin · USThe University of Texas MD Anderson Cancer Center · USUniversity of Maryland, College Park · US

Funding

Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI STROM, SARA S. · 1996 to 2011
$16.4M
NIEHS NIH HHS P30 ES007784NIEHS NIH HHS P30ES007784
6 · The paper itself

Abstract

Resveratrol is a phytochemical that has been under consideration for use as a prostate cancer chemopreventive agent. However, the efficacy, as well as the mechanisms of action of resveratrol on prostate cancer prevention, remains largely unknown. This study seeks to address these questions and examine the cancer preventive effects of resveratrol using complementary human LNCaP prostate cancer cell culture and xenograft models. In cultured LNCaP cells, we found that resveratrol inhibited cell growth. The growth inhibitory effects of resveratrol appeared to be through modulation of both androgen- and estrogen-mediated events. Global gene expression analysis using microarrays identified androgen-responsive genes as a group of genes universally affected by resveratrol in LNCaP cells in vitro. The effect of resveratrol on expression of these genes appeared to be through inhibition of both androgen- and estrogen-mediated transcription. In a xenograft model, resveratrol delayed LNCaP tumor growth and inhibited expression of a marker for steroid hormone responses. However, exposure to resveratrol also led to increased angiogenesis and inhibition of apoptosis in the xenograft. In summary, resveratrol may act through modulation of steroid hormone-dependent pathways to inhibit prostate cancer cell growth in both culture and xenografts, but exposure in vivo may be of concern.

Indexed as

AndrogensAnimalsAnticarcinogenic AgentsApoptosisCell ProliferationEstradiolGene Expression ProfilingHumansMaleMetriboloneMiceMice, Inbred BALB CNeoplasm TransplantationOligonucleotide Array Sequence AnalysisProstatic NeoplasmsReceptor, IGF Type 1AndrogensAnticarcinogenic AgentsEstradiolMetriboloneReceptor, IGF Type 1ResveratrolStilbenes

Identifiers

PMID18586690
PMCPMC2722852
OpenAlexW2104450951

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.