Evidence map›Paper›PMID 36821013›Full record

ArticleMedical oncology (Northwood, London, England)2023

Erythrose inhibits the progression to invasiveness and reverts drug resistance of cancer stem cells of glioblastoma.

Juan Carlos Gallardo-Pérez, María Cristina Trejo-Solís, Diana Xochiquetzal Robledo-Cadena, Rebeca López-Marure, Lourdes Teresa Agredano-Moreno, Luis Felipe Jimenez-García, Laura Gabriela Sánchez-Lozada

Abstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

7 authors at 3 institutions in 1 country.

Juan Carlos Gallardo-PérezDepartamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología, "Ignacio Chávez", Juan Badiano No. 1. Col Sección XVI, Tlalpan, Mexico City, Mexico. jcgallardo@ciencias.unam.mx.ORCID http://orcid.org/0000-0002-1688-3878
María Cristina Trejo-SolísLaboratorio Experimental de Enfermedades Neurodegenerativas, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.ORCID http://orcid.org/0000-0003-0233-7347
Diana Xochiquetzal Robledo-CadenaDepartamento de Bioquímica, Instituto Nacional de Cardiología, Mexico City, Mexico.ORCID http://orcid.org/0000-0002-7287-938X
Rebeca López-MarureDepartamento de Fisiología, Instituto Nacional de Cardiología, Mexico City, Mexico.ORCID http://orcid.org/0000-0003-1090-5084
Lourdes Teresa Agredano-MorenoDepartamento de Biología Celular, Facultad de Ciencias, UNAM, Mexico City, Mexico.ORCID http://orcid.org/0000-0001-7312-4141
Luis Felipe Jimenez-GarcíaDepartamento de Biología Celular, Facultad de Ciencias, UNAM, Mexico City, Mexico.ORCID http://orcid.org/0000-0003-2368-2975
Laura Gabriela Sánchez-LozadaDepartamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología, "Ignacio Chávez", Juan Badiano No. 1. Col Sección XVI, Tlalpan, Mexico City, Mexico.ORCID http://orcid.org/0000-0003-0348-9617
Instituto Nacional de Cardiología · MXUniversidad Nacional Autónoma de México · MXInstituto Nacional de Neurología y Neurocirugía · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most frequent brain cancer and more lethal than other cancers. Characteristics of this cancer are its high drug resistance, high recurrence rate and invasiveness. Invasiveness in GBM is related to overexpression of matrix metalloproteinases (MMPs) which are mediated by wnt/β-catenin and induced by the activation of signaling pathways extracellularly activated by the cytokine neuroleukin (NLK) in cancer stem cells (CSC). Therefore, in this work we evaluated the effect of the tetrose saccharide, erythrose (Ery), a NLK inhibitor of invasiveness and drug sensitization in glioblastoma stem cells (GSC). GSC were obtained from parental U373 cell line by a CSC phenotype enrichment protocol based on microenvironmental stress conditions such as hypoxia, hipoglycemia, drug exposition and serum starvation. Enriched fraction of GSC overexpressed the typical markers of brain CSC: low CD133+ and high CD44; in addition, epithelial to mesenchyme transition (EMT) markers and MMPs were increased several times in GSC vs. U373 correlating with higher invasiveness, elongated and tubular mitochondrion and temozolomide (TMZ) resistance. IC

Indexed as

Brain NeoplasmsGlioblastomaCell Line, TumorDrug Resistance, NeoplasmHumansNeoplastic Stem CellsProtein Serine-Threonine KinasesTemozolomideTetroseserythroseNLK protein, humanProtein Serine-Threonine KinasesTemozolomideTetrosesCancer stem cellsGlioblastomaInvasivenessPhytochemical

Identifiers

PMID36821013
OpenAlexW4321596520

What OpenQuestion holds

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Registered trials

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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.