Evidence map›Paper›PMID 38905127›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2024

Development of a multi-targeted chemotherapeutic approach based on G-quadruplex stabilisation and carbonic anhydrase inhibition.

Alessio Nocentini, Anna Di Porzio, Alessandro Bonardi, Carla Bazzicalupi, Andrea Petreni, Tarita Biver, Silvia Bua, Simona Marzano, Jussara Amato, Bruno Pagano and 6 more

Abstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Drug Design of Carbonic Anhydrase Inhibitors.Sub-cellular biochemistry · 2026
    Review
  2. Review
  3. Article
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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

16 authors.

Alessio NocentiniNEUROFARBA Department, Pharmaceutical and Nutraceutical Section and Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Florence, Sesto Fiorentino, Florence, Italy.
Anna Di PorzioDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Alessandro BonardiNEUROFARBA Department, Pharmaceutical and Nutraceutical Section and Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Florence, Sesto Fiorentino, Florence, Italy.ORCID 0000-0002-5520-740X
Carla BazzicalupiDepartment of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino, Florence, Italy.
Andrea PetreniNEUROFARBA Department, Pharmaceutical and Nutraceutical Section and Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Florence, Sesto Fiorentino, Florence, Italy.
Tarita BiverDepartment of Chemistry and Industrial Chemistry, University of Pisa, Pisa, Italy.
Silvia BuaResearch Institute of the University of Bucharest (ICUB), Bucharest, Romania.
Simona MarzanoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Jussara AmatoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Bruno PaganoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.ORCID 0000-0002-7716-9010
Nunzia IaccarinoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.ORCID 0000-0001-7544-5512
Stefano De TitoMolecular Cell Biology of Autophagy, The Francis Crick Institute, London, UK.
Stefano AmenteDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Naples, Italy.
Claudiu T SupuranNEUROFARBA Department, Pharmaceutical and Nutraceutical Section and Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Florence, Sesto Fiorentino, Florence, Italy.ORCID 0000-0003-4262-0323
Antonio RandazzoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Paola GratteriNEUROFARBA Department, Pharmaceutical and Nutraceutical Section and Laboratory of Molecular Modeling Cheminformatics & QSAR, University of Florence, Sesto Fiorentino, Florence, Italy.ORCID 0000-0002-9137-2509

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel class of compounds designed to hit two anti-tumour targets, G-quadruplex structures and human carbonic anhydrases (hCAs) IX and XII is proposed. The induction/stabilisation of G-quadruplex structures by small molecules has emerged as an anticancer strategy, disrupting telomere maintenance and reducing oncogene expression. hCAs IX and XII are well-established anti-tumour targets, upregulated in many hypoxic tumours and contributing to metastasis. The ligands reported feature a berberine G-quadruplex stabiliser scaffold connected to a moiety inhibiting hCAs IX and XII.

Indexed as

Antineoplastic AgentsCarbonic Anhydrase InhibitorsCarbonic Anhydrase IXCarbonic AnhydrasesDose-Response Relationship, DrugDrug Screening Assays, AntitumorG-QuadruplexesAntigens, NeoplasmCell ProliferationHeLa CellsHumansLigandsModels, MolecularMolecular StructureStructure-Activity RelationshipAntigens, NeoplasmAntineoplastic AgentsCA9 protein, humanCarbonic Anhydrase InhibitorsCarbonic Anhydrase IXCarbonic Anhydrasescarbonic anhydrase XIILigandscarbonic anhydraseG-Quadruplexmultitarget-directed ligandstumours

Identifiers

PMID38905127
PMCPMC11195807

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.