Evidence map›Paper›PMID 41175216›Full record

ReviewAnalytical and bioanalytical chemistry2026

Advancing precision medicine with bioelectroanalytical technologies leveraging unconventional nucleic acid forms.

Rebeca M Torrente-Rodríguez, Maria Gamella, Víctor Ruiz-Valdepeñas Montiel, José M Pingarrón, Susana Campuzano

Abstract readReview
PubMed Publisher
In one paragraph

Review in Analytical and bioanalytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Rebeca M Torrente-RodríguezDepartamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, Pza. de Las Ciencias 2, 28040, Madrid, Spain. rebecamt@ucm.es.
Maria GamellaDepartamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, Pza. de Las Ciencias 2, 28040, Madrid, Spain.
Víctor Ruiz-Valdepeñas MontielDepartamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, Pza. de Las Ciencias 2, 28040, Madrid, Spain.
José M PingarrónDepartamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, Pza. de Las Ciencias 2, 28040, Madrid, Spain.
Susana CampuzanoDepartamento de Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, Pza. de Las Ciencias 2, 28040, Madrid, Spain. susanacr@quim.ucm.es.

Funding

Action funded by the Community of Madrid through the Multiannual Agreement for the regulation of the cooperation framework within the Regional System of Scientific Research and Technological Innovation, signed between the Community of Madrid and the UCM, within the framework of the 6th PRICIT (Regional Plan for Scientific Research and Technological Innovation for the 2022-2025 period) from Comunidad de Madrid and Universidad Complutense de Madrid PR17/24-31891Action funded by the Community of Madrid through the Multiannual Agreement for the regulation of the cooperation framework within the Regional System of Scientific Research and Technological Innovation, signed between the Community of Madrid and the UCM, within the framework of the 6th PRICIT (Regional Plan for Scientific Research and Technological Innovation for the 2022-2025 period) from Comunidad de Madrid and Universidad Complutense de Madrid PR17/24-31912Ministerio de Ciencia e Innovación PID2022-136351OB-I00
6 · The paper itself

Abstract

The non-canonicity at the DNA and RNA levels that characterizes the intriguing world of nucleic acids is redefining our understanding of gene regulation, cellular responses, and the mechanisms that orchestrate the emergence, onset, and evolution of diseases. These atypical, mysterious, and Watson-Crick deviating DNA and RNA structural configurations include circular RNAs (circRNAs), transfer RNA-derived fragments (tRFs), G-quadruplexes (G4s), and related biotargets, such as telomerase, and are increasingly recognized as pivotal biomarkers and functional targets in precision and personalized medicine, particularly for the moment, in the neurodegenerative and oncological landscapes. Their structural uniqueness and disease-specific expression patterns and profiles position them as ideal candidates for the early diagnosis and tailored therapies. In turn, electrochemical biosensing, despite guaranteeing high sensitivity, low cost, and suitability for point-of-care applications, represents a powerful yet underutilized tool for detecting these complex promising molecular entities. Strikingly, and to the best of our knowledge, there is currently no dedicated vision addressing this important issue. Therefore, with the aim of contributing to bridge this void, this review compiles the latest efforts recently made for unlocking the diagnostic and therapeutic potentials of these enigmatic and naturally occurring biostructures and their most relevant related biotargets through the employment of bioelectroanalytical technologies.

Indexed as

Biosensing TechniquesElectrochemical TechniquesNucleic AcidsPrecision MedicineAnimalsDNAG-QuadruplexesHumansDNANucleic AcidsBioelectroanalytical technologiesBiosensingNon-canonical nucleic acidsPrecision medicine

Identifiers

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.