Evidence map›Paper›PMID 32144725›Full record

ArticleJournal of molecular neuroscience : MN2020

New Aspects of VEGF, GABA, and Glutamate Signaling in the Neocortex of Human Temporal Lobe Pharmacoresistant Epilepsy Revealed by RT-qPCR Arrays.

Rubén D Castro-Torres, Mónica E Ureña-Guerrero, Lilia M Morales-Chacón, Lourdes Lorigados-Pedre, Bárbara Estupiñan-Díaz, Luisa Rocha, Sandra Orozco-Suárez, Martha C Rivera-Cervantes, Mario Alonso-Vanegas, Carlos Beas-Zárate

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. 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
0.8field-weighted citation impact, top 34% 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, 16 citations in OpenAlex.

  1. GABACellular and molecular neurobiology · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. The neurovasculature as a target in temporal lobe epilepsy.Brain pathology (Zurich, Switzerland) · 2023
    Review
  8. Article
  9. Microvascular changes associated with epilepsy: A narrative review.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Review
  10. 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

10 authors at 5 institutions in 2 countries.

Rubén D Castro-TorresDepartamento de Biología Celular y Molecular, Centro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara, Zapopan, Jalisco, México.ORCID http://orcid.org/0000-0003-3334-3096
Mónica E Ureña-GuerreroDepartamento de Biología Celular y Molecular, Centro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara, Zapopan, Jalisco, México. murena@cucba.udg.mx.
Lilia M Morales-ChacónPrograma de Cirugía de Epilepsia, Centro Internacional de Restauración Neurológica (CIREN), Havana, Cuba.
Lourdes Lorigados-PedrePrograma de Cirugía de Epilepsia, Centro Internacional de Restauración Neurológica (CIREN), Havana, Cuba.
Bárbara Estupiñan-DíazPrograma de Cirugía de Epilepsia, Centro Internacional de Restauración Neurológica (CIREN), Havana, Cuba.
Luisa RochaDepartamento de Farmacobiología, Centro de Investigación y Estudios Avanzados (CINVESTAV) Sede Sur, México City, México.
Sandra Orozco-SuárezUnidad de Investigación Médica en Enfermedades Neurológicas, Hospital de Especialidades, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social (IMSS), México City, México.
Martha C Rivera-CervantesDepartamento de Biología Celular y Molecular, Centro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara, Zapopan, Jalisco, México.
Mario Alonso-VanegasServicio de Neurocirugía, Instituto Nacional de Neurología y Neurocirugía MVS, México City, México.
Carlos Beas-ZárateDepartamento de Biología Celular y Molecular, Centro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara, Zapopan, Jalisco, México. carlos.beas@academicos.udg.mx.
Universidad de Guadalajara · MXInternational Center of Neurologic Restoration · CUCentro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional · MXInstituto Nacional de Neurología y Neurocirugía · MXMexican Social Security Institute · MX

Funding

Consejo Nacional de Ciencia y Tecnología 177594
6 · The paper itself

Abstract

In the epilepsy spectrum, temporal lobe epilepsy (TLE) is the most common and devastating focal and symptomatic epilepsy form in adults, where more than 30% of patients develop pharmacoresistance. It is not fully understood how the gene expression contributes to establishing an epileptic phenotype. Cerebrovascular remodeling directed by VEGF (vascular endothelial growth factor) signaling might modulate the synaptic neurotransmission in the epileptic brain. To address this question, the gene expression was profiled in biopsies of the temporal cortex from diagnosed patients with pharmacoresistant TLE that underwent surgical resection to seizure control. One hundred sixty-eight genes related to VEGF signaling and GABA and glutamate neurotransmissions were evaluated. Genes related to downstream signaling -phosphoinositide 3-kinase (PI3K), mitogen-activated protein kinases (MAPK), and Janus-activated kinase/signal transducer and activator of transcription (JAK/STAT) pathways- and neurotransmitters metabolism were evaluated too. Thirty-nine genes were upregulated. The genes encoding for G protein q polypeptide, serine racemase, gephyrin, and glutamate/cystine antiporter system xCT appeared as novel upregulated genes in the pharmacoresistant TLE. ClueGO, a Cytoscape plugin, was used to build a gene network associated using Gene Ontology (GO) terminology. Enrichment analysis by ClueGO retrieves that positive regulation of endothelial cell proliferation, nerve development, and neuronal apoptosis were over-represented categories. In conclusion, VEGF signaling is confirmed as a relevant mediator in the pharmacoresistant TLE. In addition, the enrichment analysis applied to differentially expressed genes suggests new pharmacological targets to be assessed in the treatment of pharmacoresistant TLE. Results make up an approximation to better understand the epileptic brain and complement the available data.

Indexed as

TranscriptomeAdolescentAdultDrug Resistant EpilepsyEpilepsy, Temporal LobeFemaleGlutamic AcidHumansMaleMAP Kinase Signaling SystemMembrane ProteinsMiddle AgedNeocortexPhosphatidylinositol 3-KinasesRacemases and EpimerasesReceptors, GABAgephyrinGlutamic AcidMembrane ProteinsPhosphatidylinositol 3-KinasesRacemases and EpimerasesReceptors, GABASerine RacemaseVascular Endothelial Growth Factor AGABAGlutamatePharmacoresistanceRT-qPCR arrayTemporal lobe epilepsyVEGF

Identifiers

PMID32144725
OpenAlexW3010144447

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.