Evidence map›Paper›PMID 28690829›Full record

ArticleF1000Research2017

A simple mathematical approach to the analysis of polypharmacology and polyspecificity data.

Gerry Maggiora, Vijay Gokhale

Abstract read
In one paragraph

Article in F1000Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

2 authors.

Gerry MaggioraBIO5 Institute, University of Arizona, 1657 East Helen Street, Tucson, AZ, 85719, USA.ORCID 0000-0002-1839-2650
Vijay GokhaleBIO5 Institute, University of Arizona, 1657 East Helen Street, Tucson, AZ, 85719, USA.ORCID 0000-0003-2807-4741

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There many possible types of drug-target interactions, because there are a surprising number of ways in which drugs and their targets can associate with one another.  These relationships are expressed as polypharmacology and polyspecificity.  Polypharmacology is the capability of a given drug to exhibit activity with respect to multiple drug targets, which are not necessarily in the same activity class. Adverse drug reactions ('side effects') are its principal manifestation, but polypharmacology is also playing a role in the repositioning of existing drugs for new therapeutic indications.  Polyspecificity, on the other hand, is the capability of a given target to exhibit activity with respect to multiple, structurally dissimilar drugs.  That these concepts are closely related to one another is, surprisingly, not well known.  It will be shown in this work that they are, in fact, mathematically related to one another and are in essence 'two sides of the same coin'.  Hence, information on polypharmacology provides equivalent information on polyspecificity, and

Indexed as

bipartite networksdrugsdrug targetsedge-coloredlatent informationnetworkspolypharmacologypolyspecificity

Identifiers

PMID28690829
PMCPMC5482344

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.