Evidence map›Paper›PMID 31001564›Full record

ReviewJournal of immunology research2019

Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells.

Rodolfo Soria-Castro, Alejandro Schcolnik-Cabrera, Gloria Rodríguez-López, Marcia Campillo-Navarro, Nahum Puebla-Osorio, Sergio Estrada-Parra, Iris Estrada-García, Rommel Chacón-Salinas, Alma D Chávez-Blanco

Open access · goldAbstract readReview
In one paragraph

Review in Journal of immunology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 68 citations in OpenAlex.

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  18. Integrative computational approach identifies drug targets in CD4NPJ systems biology and applications · 2021
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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 4 institutions in 2 countries.

Rodolfo Soria-CastroDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (ENCB-IPN), Mexico City, Mexico.ORCID 0000-0003-1884-8950
Alejandro Schcolnik-CabreraSubdirección de Investigación Básica, Instituto Nacional de Cancerología (INCan), México City, Mexico.ORCID 0000-0001-7734-3253
Gloria Rodríguez-LópezDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (ENCB-IPN), Mexico City, Mexico.ORCID 0000-0001-5342-3806
Marcia Campillo-NavarroLaboratorio de Inmunología Integrativa, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas, Mexico City, Mexico.
Nahum Puebla-OsorioDepartment of Lymphoma and Myeloma, The University of Texas, MD Anderson, Cancer Center, Houston, TX, USA.
Sergio Estrada-ParraDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (ENCB-IPN), Mexico City, Mexico.
Iris Estrada-GarcíaDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (ENCB-IPN), Mexico City, Mexico.ORCID 0000-0002-5312-1979
Rommel Chacón-SalinasDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (ENCB-IPN), Mexico City, Mexico.ORCID 0000-0002-4500-0253
Alma D Chávez-BlancoSubdirección de Investigación Básica, Instituto Nacional de Cancerología (INCan), México City, Mexico.ORCID 0000-0002-4201-5935
Instituto Politécnico Nacional · MXInstituto Nacional de Cancerología · MXInstituto Nacional de Enfermedades Respiratorias · MXThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Valproic acid (VPA) is widely recognized for its use in the control of epilepsy and other neurological disorders in the past 50 years. Recent evidence has shown the potential of VPA in the control of certain cancers, owed in part to its role in modulating epigenetic changes through the inhibition of histone deacetylases, affecting the expression of genes involved in the cell cycle, differentiation, and apoptosis. The direct impact of VPA in cells of the immune system has only been explored recently. In this review, we discuss the effects of VPA in the suppression of some activation mechanisms in several immune cells that lead to an anti-inflammatory response. As expected, immune cells are not exempt from the effect of VPA, as it also affects the expression of genes of the cell cycle and apoptosis through epigenetic modifications. In addition to inhibiting histone deacetylases, VPA promotes RNA interference, activates histone methyltransferases, or represses the activation of transcription factors. However, during the infectious process, the effectiveness of VPA is subject to the biological nature of the pathogen and the associated immune response; this is because VPA can promote the control or the progression of the infection. Due to its various effects, VPA is a promising alternative for the control of autoimmune diseases and hypersensitivity and needs to be further explored.

Indexed as

Adaptive ImmunityDrug RepositioningImmunity, InnateAnimalsApoptosisCell CycleCell DifferentiationCell Line, TumorCell ProliferationEpigenesis, GeneticHistone Deacetylase InhibitorsHistone DeacetylasesHumansMiceNeoplasmsRNA InterferenceHistone Deacetylase InhibitorsHistone DeacetylasesValproic Acid

Identifiers

PMID31001564
PMCPMC6437734
OpenAlexW2920958972

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.