Evidence map›Paper›PMID 34677434›Full record

ArticleMarine drugs2021

Dual Targeting of PTP1B and Aldose Reductase with Marine Drug Phosphoeleganin: A Promising Strategy for Treatment of Type 2 Diabetes.

Massimo Genovese, Concetta Imperatore, Marcello Casertano, Anna Aiello, Francesco Balestri, Lucia Piazza, Marialuisa Menna, Antonella Del Corso, Paolo Paoli

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Massimo GenoveseDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Viale Morgagni 50, 50134 Florence, Italy.ORCID 0000-0002-3732-3124
Concetta ImperatoreDepartment of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131 Napoli, Italy.ORCID 0000-0001-7377-0653
Marcello CasertanoDepartment of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131 Napoli, Italy.ORCID 0000-0001-5037-712X
Anna AielloDepartment of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131 Napoli, Italy.
Francesco BalestriBiochemistry Unit, Department of Biology, University of Pisa, Via S. Zeno, 51, 56123 Pisa, Italy.
Lucia PiazzaBiochemistry Unit, Department of Biology, University of Pisa, Via S. Zeno, 51, 56123 Pisa, Italy.
Marialuisa MennaDepartment of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131 Napoli, Italy.ORCID 0000-0002-4515-3014
Antonella Del CorsoBiochemistry Unit, Department of Biology, University of Pisa, Via S. Zeno, 51, 56123 Pisa, Italy.ORCID 0000-0003-3165-6128
Paolo PaoliDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, Viale Morgagni 50, 50134 Florence, Italy.ORCID 0000-0001-6448-7266
University of Naples Federico II · ITUniversity of Pisa · ITUniversity of Florence · IT

Funding

Regione Campania B61G18000470007Università degli Studi di Firenze Fondi di Ateneo 2020Università degli Studi di Napoli Federico II Department of Pharmacy-Bando Contributo alla ricerca anno 2021Università di Pisa Fondi di Ateneo 2020
6 · The paper itself

Abstract

An in-depth study on the inhibitory mechanism on protein tyrosine phosphatase 1B (PTP1B) and aldose reductase (AR) enzymes, including analysis of the insulin signalling pathway, of phosphoeleganin, a marine-derived phosphorylated polyketide, was achieved. Phosphoeleganin was demonstrated to inhibit both enzymes, acting respectively as a pure non-competitive inhibitor of PTP1B and a mixed-type inhibitor of AR. In addition, in silico docking analyses to evaluate the interaction mode of phosphoeleganin with both enzymes were performed. Interestingly, this study showed that phosphoeleganin is the first example of a dual inhibitor polyketide extracted from a marine invertebrate, and it could be used as a versatile scaffold structure for the synthesis of new designed multiple ligands.

Indexed as

UrochordataAldehyde ReductaseAnimalsAquatic OrganismsDiabetes Mellitus, Type 2Hep G2 CellsHumansHypoglycemic AgentsMediterranean SeaMolecular Docking SimulationPolyketidesProtein Tyrosine Phosphatase, Non-Receptor Type 1Signal TransductionAldehyde ReductaseHypoglycemic AgentsphosphoeleganinPolyketidesProtein Tyrosine Phosphatase, Non-Receptor Type 1aldose reductasemarine natural productsmetabolic diseasesmultitarget drugsprotein tyrosine phosphatase 1Btype 2 diabetes mellitus

Identifiers

PMID34677434
PMCPMC8540617
OpenAlexW3198950284

What OpenQuestion holds

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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.