Evidence map›Paper›PMID 42889945›Full record

ArticleFrontiers in chemistry2026

Development of novel Copper(II)-hydrazone complexes for targeting the inhibition of human osteosarcoma growth.

Lucía Santa Maria de la Parra, Olivia Espindola-Moreno, Matías H Assandri, Gustavo A Echeverría, Oscar E Piro, Gonzalo Scalese, Ignacio E León

Abstract read
In one paragraph

Article in Frontiers in 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.

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0citing papers in PubMed
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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

7 authors.

Lucía Santa Maria de la ParraDepartamento de Química, Facultad de Ciencias Exactas, CEQUINOR (UNLP, CCT-CONICET La Plata, asociado a CIC), Universidad Nacional de La Plata, La Plata, Argentina.
Olivia Espindola-MorenoDepartamento de Química, Facultad de Ciencias Exactas, CEQUINOR (UNLP, CCT-CONICET La Plata, asociado a CIC), Universidad Nacional de La Plata, La Plata, Argentina.
Matías H AssandriDepartamento de Ciencias Biológicas, Cátedra de Microbiología, Facultad de Ciencias Exactas, Universidad Nacional de La Plata (UNLP), La Plata, Argentina.
Gustavo A EcheverríaDepartamento de Física, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina.
Oscar E PiroDepartamento de Física, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, La Plata, Argentina.
Gonzalo ScaleseDepartamento Estrella Campos, Área Química Inorgánica, Facultad de Química, Universidad de la República, Montevideo, Uruguay.
Ignacio E LeónDepartamento de Química, Facultad de Ciencias Exactas, CEQUINOR (UNLP, CCT-CONICET La Plata, asociado a CIC), Universidad Nacional de La Plata, La Plata, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Osteosarcoma (OS) is the most common primary malignant bone tumor in children and young adults and remains associated with poor clinical outcomes due to recurrence, metastasis, and resistance to conventional chemotherapy. In recent years, copper-based compounds have emerged as promising anticancer agents because of their unique redox properties and ability to target multiple cellular pathways. Methods: In this work, we synthesized and characterized two hydrazone ligands, ( Results: Biological evaluation demonstrated that coordination to Cu(II) converted the inactive hydrazone ligands into highly potent anticancer agents. Both Cu(II) complexes exhibited potent cytotoxic activity in 2D cell cultures, with IC Discussion: Among the compounds studied, the binuclear complex Cu

Indexed as

cancercopperhydrazonesosteosarcomareactive oxygen species

Identifiers

PMID42889945
PMCPMC13670372

What OpenQuestion holds

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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.