Evidence map›Paper›PMID 41157115›Full record

ReviewMolecules (Basel, Switzerland)2025

Molecular Tools for Precision Targeting and Detection of G-Quadruplex Structures.

Daniele Esposito, Alessandra Locatelli, Rita Morigi

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. 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

3 authors.

Daniele EspositoDepartment of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.
Alessandra LocatelliDepartment of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.ORCID 0000-0003-2026-4698
Rita MorigiDepartment of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.ORCID 0000-0003-4739-8733

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the context of the study of G-quadruplex (G4), the main field of focus is usually referred to binding molecules able to interact with these non-canonical conformations and stabilizing them leading to diverse biological effects. Although the cellular events triggered by these ligands are useful for potential anticancer applications, the development of innovative molecular tools to gain new information about G4 has become more urgent. The concept of G4-interacting molecular tools refers to chemical entities that can bind and interact with G-rich sequences of the genome-like traditional ligands-but simultaneously provide external outputs that can be interpreted and studied to obtain insights on their dynamics, position in the cellular context and more. Starting from traditional chemical approaches, researchers have worked to produce sophisticated and complex synthetic strategies in order to introduce more accurate instruments for their aims. This review provides a comprehensive and up-to-date overview of this research area by detailing the major classes of molecular tools, describing the latest updates about three main classes: small-molecules fluorescence probes, G4-binding metal complexes, and products of conjugation strategies. Overall, advancements in molecular tools targeting G4s have made the study of G4 formation, dynamics, and functions much easier; thus, increasing the knowledge of G4 biology, and creating new opportunities for biomedical and therapeutic applications, ultimately highlighting the importance of the development of molecular tools in G4 research.

Indexed as

G-QuadruplexesCoordination ComplexesFluorescent DyesHumansLigandsCoordination ComplexesFluorescent DyesLigandsconjugatesfluorescent probesG-quadruplexmetal complexesmolecular tools

Identifiers

PMID41157115
PMCPMC12565907

What OpenQuestion holds

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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.