Evidence map›Paper›PMID 21555001›Full record

ReviewJournal of proteomics2011

Proteomic identification of binding targets of isothiocyanates: A perspective on techniques.

Lixin Mi, Zhen Xiao, Timothy D Veenstra, Fung-Lung Chung

Abstract readReview
In one paragraph

Review in Journal of proteomics, 2011. 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
–field-weighted citation impact
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.

  1. Article
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  8. Review
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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

4 authors.

Lixin MiDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA. lm293@georgetown.edu
Zhen Xiao
Timothy D Veenstra
Fung-Lung Chung

Funding

Mechanisms of Chemoprevention by IsothiocyanatesR01CA100853 · NCI · GEORGETOWN UNIVERSITY · PI CHUNG, FUNG-LUNG · 2004 to 2014
$3.3M
NCI NIH HHS CA100853NCI NIH HHS R01 CA100853
6 · The paper itself

Abstract

Intake of cruciferous vegetable is inversely associated with the risk of several cancer types. Isothiocyanates (ITCs) are believed to be important constituents contributing to these cancer-preventive effects. Although several mechanisms, including induction of apoptosis, have been proposed for the anti-carcinogenesis activities of ITCs, detailed upstream triggering events are still not fully understood. Identification of ITC binding targets in cellular proteins is crucial for not only mechanistic studies but also future drug screening and design. In this review, we summarize recent progress in discovery of ITC protein targets from a technical perspective. The advantages and limitations of each method are discussed to facilitate future studies on target discovery of ITCs and perhaps other compounds.

Indexed as

Binding SitesAnticarcinogenic AgentsChromatography, AffinityElectrophoresis, Gel, Two-DimensionalIsothiocyanatesProtein BindingProtein ConformationProteomicsTandem Mass SpectrometryTubulinAnticarcinogenic AgentsIsothiocyanatesTubulin

Identifiers

PMID21555001
PMCPMC3107917

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.