Evidence map›Paper›PMID 35878167›Full record

ArticleToxins2022

In Vitro Toxicity Evaluation of Cyanotoxins Cylindrospermopsin and Microcystin-LR on Human Kidney HEK293 Cells.

Leticia Diez-Quijada, María Puerto, Daniel Gutiérrez-Praena, Maria V Turkina, Alexandre Campos, Vitor Vasconcelos, Ana M Cameán, Ángeles Jos

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 26% 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, 12 citations in OpenAlex.

  1. Review
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  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

8 authors at 3 institutions in 3 countries.

Leticia Diez-QuijadaArea of Toxicology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.ORCID 0000-0002-3523-9287
María PuertoArea of Toxicology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
Daniel Gutiérrez-PraenaArea of Toxicology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.
Maria V TurkinaDepartment of Biomedical and Clinical Sciences, Faculty of Medicine and Health Sciences, Linköping University, 581 83 Linköping, Sweden.
Alexandre CamposCIIMAR/CIMAR-Interdisciplinary Centre of Marine and Environmental Research, University of Porto, 4450-208 Matosinhos, Portugal.ORCID 0000-0003-4621-885X
Vitor VasconcelosCIIMAR/CIMAR-Interdisciplinary Centre of Marine and Environmental Research, University of Porto, 4450-208 Matosinhos, Portugal.ORCID 0000-0003-3585-2417
Ana M CameánArea of Toxicology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.ORCID 0000-0003-1524-748X
Ángeles JosArea of Toxicology, Faculty of Pharmacy, Universidad de Sevilla, 41012 Seville, Spain.ORCID 0000-0001-7546-3294
Universidad de Sevilla · ESUniversidade do Porto · PTLinköping University · SE

Funding

Marie Curie grant agreement No 823860
6 · The paper itself

Abstract

Cyanotoxins are secondary metabolites produced by different types of cyanobacteria. Among them, Cylindrospermopsin (CYN) and Microcystins (MCs) stand out due to their wide geographical distribution and toxicity in various organs, including the kidney, which is involved in their distribution and elimination. However, the renal toxicity caused by CYN and MCs has hardly been studied. The aim of this work was to assess the cytotoxicity effects caused by CYN and MC-LR in the renal cell line HEK293, and for the first time, the influence of CYN on the gene expression of selected genes in these cells by quantitative real-time PCR (qRT-PCR). CYN caused an upregulation in the gene expression after exposure to the highest concentration (5 µg/mL) and the longest time of exposure (24 h). Moreover, shotgun proteomic analysis was used to assess the molecular responses of HEK293 cells after exposure to the individuals and combinations of CYN + MC-LR. The simultaneous exposure to both cyanotoxins caused a greater number of alterations in protein expression compared to single toxins, causing changes in the cellular, lipid and protein metabolism and in protein synthesis and transport. Further studies are needed to complete the toxicity molecular mechanisms of both CYN and MC-LR at the renal level.

Indexed as

Bacterial ToxinsMicrocystinsAlkaloidsCyanobacteria ToxinsHEK293 CellsHumansKidneyMarine ToxinsProteomicsAlkaloidsBacterial ToxinsCyanobacteria Toxinscyanoginosin LRcylindrospermopsinMarine ToxinsMicrocystinsCylindrospermopsinHEK293 cellsMicrocystin-LRqRT-PCRshotgun proteomics

Identifiers

PMID35878167
PMCPMC9316492
OpenAlexW4283361036

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.