Evidence map›Paper›PMID 41303683›Full record

ArticleInternational journal of molecular sciences2025

Dysregulated lncRNAs in Cisplatin-Induced Nephrotoxicity and Their Association with Apoptosis and Autophagy: An Exploratory In Vitro Study.

Yuliannis Lugones, Pía Loren, Carola E Matus, Nelia M Rodriguez, Pamela Leal-Rojas, Rody San Martín, Kathleen Saavedra, Nicolás Saavedra, Patricia Moriel, Luis A Salazar

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Yuliannis LugonesDoctoral Program in Sciences Major in Applied Cellular and Molecular Biology, Universidad de La Frontera, Temuco 4811230, Chile.
Pía LorenCenter of Molecular Biology and Pharmacogenetics, Department of Basic Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.ORCID 0000-0001-9814-8107
Carola E MatusCenter of Molecular Biology and Pharmacogenetics, Department of Basic Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.
Nelia M RodriguezDepartamento de Ciencias Biológicas, Instituto de Ciencias Biomédicas, Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Temuco 4810101, Chile.
Pamela Leal-RojasCenter of Excellence in Translational Medicine (CEMT) & Scientific and Technological Bioresource Nucleus (BIOREN), Universidad de La Frontera, Temuco 4810296, Chile.
Rody San MartínMolecular Pathology Laboratory, Institute of Biochemistry and Microbiology, Science Faculty, Universidad Austral de Chile, Valdivia 5110566, Chile.
Kathleen SaavedraCenter of Molecular Biology and Pharmacogenetics, Department of Basic Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.ORCID 0000-0001-5729-8854
Nicolás SaavedraCenter of Molecular Biology and Pharmacogenetics, Department of Basic Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.ORCID 0000-0002-3334-5107
Patricia MorielSchool of Medical Sciences, University of Campinas, Campinas 13083887, SP, Brazil.ORCID 0000-0002-4927-7022
Luis A SalazarCenter of Molecular Biology and Pharmacogenetics, Department of Basic Sciences, Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.ORCID 0000-0002-5112-6944

Funding

Agencia Nacional de Investigación y Desarrollo ANID-FAPESP 19/13250-1
6 · The paper itself

Abstract

Cisplatin is a widely used chemotherapeutic agent, but its clinical application is limited by nephrotoxicity. Conventional renal markers lack sensitivity for early cisplatin nephrotoxicity while long non-coding RNAs (lncRNAs) display cisplatin-responsive changes with exploratory value. The present study aimed to explore the differential expression of eight lncRNAs on in vitro model of cisplatin-induced nephrotoxicity. Human kidney cell lines HEK-293 and HK-2 were exposed to increasing concentrations of cisplatin for 24 h. Cell viability was determined by colorimetric assays to ascertain the concentrations resulting in 25% (IC

Indexed as

Antineoplastic AgentsApoptosisAutophagyCisplatinRNA, Long NoncodingCell LineCell SurvivalGene Expression RegulationHEK293 CellsHumansKidneyAntineoplastic AgentsCisplatinRNA, Long NoncodingapoptosisautophagycisplatinlncRNAnephrotoxicity

Identifiers

PMID41303683
PMCPMC12653642

What Socratic 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 Socratic graph.