Evidence map›Paper›PMID 21401048›Full record

ArticleJournal of agricultural and food chemistry2011

Resveratrol metabolites do not elicit early pro-apoptotic mechanisms in neuroblastoma cells.

Jason D Kenealey, Lalita Subramanian, Paul R Van Ginkel, Soesiawati Darjatmoko, Mary J Lindstrom, Veronika Somoza, Sunil K Ghosh, Zhenlei Song, Richard P Hsung, Glen S Kwon and 3 more

Abstract read
In one paragraph

Article in Journal of agricultural and food chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 44 citations in OpenAlex.

  1. Focus on the Use of Resveratrol in Bladder Cancer.International journal of molecular sciences · 2023
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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

13 authors at 2 institutions in 2 countries.

Jason D KenealeyDepartment of Biomolecular Chemistry, Medical Science Center, University of Wisconsin, Madison, Wisconsin 53705, United States.
Lalita Subramanian
Paul R Van Ginkel
Soesiawati Darjatmoko
Mary J Lindstrom
Veronika Somoza
Sunil K Ghosh
Zhenlei Song
Richard P Hsung
Glen S Kwon
Kevin W Eliceiri
Daniel M Albert
Arthur S Polans
University of Wisconsin–Madison · USUniversity of Vienna · AT

Funding

Angiogenic Factors Associated with Uveal MelanomaR01CA103653 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI POLANS, ARTHUR S · 2004 to 2007
$1.6M
NCI NIH HHS R01 CA103653NCI NIH HHS R01CA103653
6 · The paper itself

Abstract

Resveratrol, a nontoxic polyphenol, has been shown to inhibit tumor growth in a xenograft mouse model of neuroblasoma. However, resveratrol is rapidly metabolized, mainly to its glucuronidated and sulfated derivatives. This study demonstrates that resveratrol alone, and not the glucuronidated or sulfated metabolites, is taken up into tumor cells, induces a rise in [Ca(2+)](i), and ultimately leads to a decrease in tumor cell viability. A new water-soluble resveratrol formulation was delivered directly at the site of the tumor in a neuroblastoma mouse model. The amount of unmodified resveratrol associated with the tumor increased more than 1000-fold. The increase of unmodified resveratrol associated with the tumor resulted in tumor regression. The number of residual tumor cells that remained viable also decreased as the ratio of the metabolites relative to unmodified resveratrol declined.

Indexed as

AnimalsApoptosisCell Line, TumorCell SurvivalFemaleHumansMiceMice, NudeNeuroblastomaResveratrolStilbenesResveratrolStilbenes

Identifiers

PMID21401048
PMCPMC3099401
OpenAlexW2331080292

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.