Evidence map›Paper›PMID 27768030›Full record

ArticleJournal of visualized experiments : JoVE2016

Mimicking the Function of Signaling Proteins: Toward Artificial Signal Transduction Therapy.

Ronny Peri-Naor, Leila Motiei, David Margulies

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

3 authors at 1 institution in 1 country.

Ronny Peri-NaorDepartment of Organic Chemistry, Weizmann Institute of Science.
Leila MotieiDepartment of Organic Chemistry, Weizmann Institute of Science.
David MarguliesDepartment of Organic Chemistry, Weizmann Institute of Science; david.margulies@weizmann.ac.il.
Weizmann Institute of Science · IL

Funding

European Research Council 338265
6 · The paper itself

Abstract

Signal transduction pathways, which control the response of cells to various environmental signals, are mediated by the function of signaling proteins that interact with each other and activate one other with high specificity. Synthetic agents that mimic the function of these proteins might therefore be used to generate unnatural signal transduction steps and consequently, alter the cell's function. We present guidelines for designing 'chemical transducers' that can induce artificial communication between native proteins. In addition, we present detailed protocols for synthesizing and testing a specific 'transducer', which can induce communication between two unrelated proteins: platelet-derived growth-factor (PDGF) and glutathione-S-transferase (GST). The way by which this unnatural PDGF-GST communication could be used to control the cleavage of an anticancer prodrug is also presented, indicating the potential for using such systems in 'artificial signal transduction therapy'. This work is intended to facilitate developing additional 'transducers' of this class, which may be used to mediate intracellular protein-protein communication and consequently, to induce artificial cell signaling pathways.

Indexed as

Chemistry Techniques, SyntheticProdrugsAntineoplastic AgentsAptamers, NucleotideAzo CompoundsCell Physiological PhenomenaGlutathione TransferaseNitric OxidePiperazinesPlatelet-Derived Growth FactorSignal TransductionAntineoplastic AgentsAptamers, NucleotideAzo CompoundsGlutathione TransferaseNitric OxideO(2)-(2,4-dinitrophenyl) 1-((4-ethoxycarbonyl)piperazin-1-yl)diazen-1-ium-1,2-diolatePiperazinesPlatelet-Derived Growth FactorProdrugs

Identifiers

PMID27768030
PMCPMC5092080
OpenAlexW2527581597

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.