Evidence map›Paper›PMID 32535722›Full record

ArticleCellular and molecular neurobiology2021

Landscape of Germline Genetic Variants in AGT, MGMT, and TP53 in Mexican Adult Patients with Astrocytoma.

José Alberto Carlos-Escalante, Liliana Gómez-Flores-Ramos, Xiaopeng Bian, Alexander Perdomo-Pantoja, Kelvin César de Andrade, Sonia Iliana Mejía-Pérez, Bernardo Cacho-Díaz, Rodrigo González-Barrios, Nancy Reynoso-Noverón, Ernesto Soto-Reyes and 16 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

26 authors at 8 institutions in 3 countries.

José Alberto Carlos-Escalante *PECEM (MD/PhD), Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-8445-9198
Liliana Gómez-Flores-Ramos *Cátedras CONACYT- Instituto Nacional de Salud Pública, 62100, Cuernavaca, Morelos, Mexico.ORCID https://orcid.org/0000-0002-4617-639X
Xiaopeng BianComputational Genomics and Bioinformatics Group, Center for Biomedical Informatics and Information Technology, National Cancer Institute, NIH, Rockville, MD, 20850, USA.ORCID https://orcid.org/0000-0003-1167-0053
Alexander Perdomo-PantojaDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.ORCID https://orcid.org/0000-0002-4981-8132
Kelvin César de AndradeClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Rockville, MD, 20850, USA.ORCID https://orcid.org/0000-0003-4651-996X
Sonia Iliana Mejía-PérezDepartamento de Enseñanza, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suárez", 13269, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-5929-6761
Bernardo Cacho-DíazUnidad de Neurociencia, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-9289-5312
Rodrigo González-BarriosDirección de Investigación, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-8982-6586
Nancy Reynoso-NoverónDirección de Investigación, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-7784-2287
Ernesto Soto-ReyesDepartamento de Ciencias Naturales, Universidad Autónoma Metropolitana-Cuajimalpa, 05370, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-4219-6406
Thalía Estefanía Sánchez-CorreaDepartamento de Neurocirugía, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez", 14269, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-9133-6746
Lissania Guerra-CalderasDepartamento de Ciencias Naturales, Universidad Autónoma Metropolitana-Cuajimalpa, 05370, Mexico City, Mexico.ORCID https://orcid.org/0000-0003-3443-4803
Chunhua YanComputational Genomics and Bioinformatics Group, Center for Biomedical Informatics and Information Technology, National Cancer Institute, NIH, Rockville, MD, 20850, USA.ORCID https://orcid.org/0000-0001-5474-7431
Qingrong ChenComputational Genomics and Bioinformatics Group, Center for Biomedical Informatics and Information Technology, National Cancer Institute, NIH, Rockville, MD, 20850, USA.ORCID https://orcid.org/0000-0003-1325-6147
Clementina Castro-HernándezUnidad de Epidemiología E Investigación Biomédica en Cáncer, Instituto de Investigaciones Biomédicas, UNAM-INCAN, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-5641-3627
Silvia Vidal-MillánClínica de Cáncer Hereditario, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-7312-9428
Lucía Taja-ChayebDirección de Investigación, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-9592-8527
Olga GutiérrezDirección de Investigación, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-5493-6774
Rosa María Álvarez-GómezClínica de Cáncer Hereditario, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-5458-7201
Juan Luis Gómez-AmadorDepartamento de Neurocirugía, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez", 14269, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-2115-5728
Patricia Ostrosky-WegmanInstituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, 04510, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-8564-3472
Alejandro Mohar-BetancourtUnidad de Epidemiología E Investigación Biomédica en Cáncer, Instituto de Investigaciones Biomédicas, UNAM-INCAN, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-4730-4787
Luis Alonso Herrera-MontalvoUnidad de Epidemiología E Investigación Biomédica en Cáncer, Instituto de Investigaciones Biomédicas, UNAM-INCAN, 14080, Mexico City, Mexico.ORCID https://orcid.org/0000-0003-3998-9306
Teresa CoronaLaboratorio Clínico de Enfermedades Neurodegenerativas, Instituto Nacional de Neurología y Neurocirugía, Manuel Velasco Suárez", 14269, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-9324-229X
Daoud MeerzamanComputational Genomics and Bioinformatics Group, Center for Biomedical Informatics and Information Technology, National Cancer Institute, NIH, Rockville, MD, 20850, USA.ORCID https://orcid.org/0000-0002-0129-5256
Talia Wegman-OstroskyDirección de Investigación, Instituto Nacional de Cancerología, 14080, Mexico City, Mexico. taliaw@gmail.com.ORCID http://orcid.org/0000-0002-3207-6697
Instituto Nacional de Cancerología · MXNational Cancer Institute · USInstituto Nacional de Neurología y Neurocirugía · MXUniversidad Autónoma Metropolitana · MXUniversidad Nacional Autónoma de México · MXInstituto Nacional de Salud Pública · MXJohns Hopkins University · USNational Institute of Genomic Medicine · MX

Funding

Consejo Nacional de Ciencia y Tecnología 969754Consejo Nacional de Ciencia y Tecnología Salud-2013-01-202720
6 · The paper itself

Abstract

Astrocytoma is the most common type of primary brain tumor. The risk factors for astrocytoma are poorly understood; however, germline genetic variants account for 25% of the risk of developing gliomas. In this study, we assessed the risk of astrocytoma associated with variants in AGT, known by its role in angiogenesis, TP53, a well-known tumor suppressor and the DNA repair gene MGMT in a Mexican population. A case-control study was performed in 49 adult Mexican patients with grade II-IV astrocytoma. Sequencing of exons and untranslated regions of AGT, MGMT, and TP53 from was carried in an Ion Torrent platform. Individuals with Mexican Ancestry from the 1000 Genomes Project were used as controls. Variants found in our cohort were then assessed in a The Cancer Genome Atlas astrocytoma pan-ethnic validation cohort. Variants rs1926723 located in AGT (OR 2.74, 1.40-5.36 95% CI), rs7896488 in MGMT (OR 3.43, 1.17-10.10 95% CI), and rs4968187 in TP53 (OR 2.48, 1.26-4.88 95% CI) were significantly associated with the risk of astrocytoma after multiple-testing correction. This is the first study where the AGT rs1926723 variant, TP53 rs4968187, and MGMT rs7896488 were found to be associated with the risk of developing an astrocytoma.

Indexed as

AdultAngiotensinogenAstrocytomaBrain NeoplasmsCase-Control StudiesCohort StudiesDNA Modification MethylasesDNA Repair EnzymesFemaleGene Expression Regulation, NeoplasticGenetic VariationHumansMaleMexicoMiddle AgedTumor Suppressor Protein p53AGT protein, humanAngiotensinogenDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanTP53 protein, humanTumor Suppressor Protein p53Tumor Suppressor ProteinsAstrocytomaGermline genetic variantMexican populationRisk

Identifiers

PMID32535722
PMCPMC11448676
OpenAlexW3034991885

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.