Evidence map›Paper›PMID 33525510›Full record

ArticleInternational journal of molecular sciences2021

Known Drugs Identified by Structure-Based Virtual Screening Are Able to Bind Sigma-1 Receptor and Increase Growth of Huntington Disease Patient-Derived Cells.

Theo Battista, Gianmarco Pascarella, David Sasah Staid, Gianni Colotti, Jessica Rosati, Annarita Fiorillo, Alessia Casamassa, Angelo Luigi Vescovi, Barbara Giabbai, Marta Stefania Semrau and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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

15 authors at 6 institutions in 1 country.

Theo BattistaInstitute of Molecular Biology and Pathology, National Research Council of Italy, 00185 Rome, Italy.ORCID 0000-0001-8401-890X
Gianmarco PascarellaInstitute of Molecular Biology and Pathology, National Research Council of Italy, 00185 Rome, Italy.
David Sasah StaidInstitute of Molecular Biology and Pathology, National Research Council of Italy, 00185 Rome, Italy.ORCID 0000-0003-0652-0974
Gianni ColottiInstitute of Molecular Biology and Pathology, National Research Council of Italy, 00185 Rome, Italy.ORCID 0000-0002-9913-0635
Jessica RosatiCellular Reprogramming Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-4483-386X
Annarita FiorilloDepartment of Biochemical Sciences "A. Rossi Fanelli", "Sapienza" University, 00185 Rome, Italy.ORCID 0000-0002-8966-8554
Alessia CasamassaCellular Reprogramming Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
Angelo Luigi VescoviCellular Reprogramming Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
Barbara GiabbaiProtein Facility, Structural Biology Lab, Elettra Sincrotrone Trieste, 34149 Basovizza, Italy.
Marta Stefania SemrauProtein Facility, Structural Biology Lab, Elettra Sincrotrone Trieste, 34149 Basovizza, Italy.ORCID 0000-0002-0642-3034
Sergio FanelliHuntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0001-5832-8381
Paola StoriciProtein Facility, Structural Biology Lab, Elettra Sincrotrone Trieste, 34149 Basovizza, Italy.ORCID 0000-0002-2590-3332
Ferdinando SquitieriHuntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-7397-1727
Veronica MoreaInstitute of Molecular Biology and Pathology, National Research Council of Italy, 00185 Rome, Italy.
Andrea IlariInstitute of Molecular Biology and Pathology, National Research Council of Italy, 00185 Rome, Italy.ORCID 0000-0002-7754-399X
Institute of Molecular Biology and Pathology · ITCasa Sollievo della Sofferenza · ITElettra-Sincrotrone Trieste S.C.p.A. · ITSapienza University of Rome · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Trento · IT

Funding

Ministero della Salute RF-2016-02364123Ministero della Salute Ricerca Corrente 2019-2020Ministero dell'Istruzione, dell'Università e della Ricerca 2017483NH8_005
6 · The paper itself

Abstract

Huntington disease (HD) is a devastating and presently untreatable neurodegenerative disease characterized by progressively disabling motor and mental manifestations. The sigma-1 receptor (σ1R) is a protein expressed in the central nervous system, whose 3D structure has been recently determined by X-ray crystallography and whose agonists have been shown to have neuroprotective activity in neurodegenerative diseases. To identify therapeutic agents against HD, we have implemented a drug repositioning strategy consisting of: (i) Prediction of the ability of the FDA-approved drugs publicly available through the ZINC database to interact with σ1R by virtual screening, followed by computational docking and visual examination of the 20 highest scoring drugs; and (ii) Assessment of the ability of the six drugs selected by computational analyses to directly bind purified σ1R in vitro by Surface Plasmon Resonance and improve the growth of fibroblasts obtained from HD patients, which is significantly impaired with respect to control cells. All six of the selected drugs proved able to directly bind purified σ1R in vitro and improve the growth of HD cells from both or one HD patient. These results support the validity of the drug repositioning procedure implemented herein for the identification of new therapeutic tools against HD.

Indexed as

AdultCell ProliferationCells, CulturedComputer SimulationDatabases, PharmaceuticalDrug Evaluation, PreclinicalDrug RepositioningFibroblastsHumansHuntington DiseaseMaleMiddle AgedModels, MolecularMolecular Docking SimulationPharmaceutical PreparationsProtein ConformationPharmaceutical PreparationsReceptors, sigmaSigma-1 Receptorcellular modelscomputational dockingdrug repositioningHuntington disease (HD)sigma-1 receptor (σ1R)structure analysissurface plasmon resonance (SPR)virtual screening

Identifiers

PMID33525510
PMCPMC7865886
OpenAlexW3125741175

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.