Evidence map›Paper›PMID 36066676›Full record

ArticleCellular and molecular life sciences : CMLS2022

Potent anticancer activity of a novel iridium metallodrug via oncosis.

Enrique Ortega-Forte, Samanta Hernández-García, Gloria Vigueras, Paula Henarejos-Escudero, Natalia Cutillas, José Ruiz, Fernando Gandía-Herrero

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
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

10 citing papers in PubMed, 34 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Enrique Ortega-Forte *Departamento de Química Inorgánica, Universidad de Murcia, and Murcia BioHealth Research Institute (IMIB-Arrixaca), 30071, Murcia, Spain.
Samanta Hernández-García *Departamento de Bioquímica y Biología Molecular A. Unidad Docente de Biología, Facultad de Veterinaria, Universidad de Murcia, 30071, Murcia, Spain.
Gloria Vigueras *Departamento de Química Inorgánica, Universidad de Murcia, and Murcia BioHealth Research Institute (IMIB-Arrixaca), 30071, Murcia, Spain.
Paula Henarejos-EscuderoDepartamento de Bioquímica y Biología Molecular A. Unidad Docente de Biología, Facultad de Veterinaria, Universidad de Murcia, 30071, Murcia, Spain.
Natalia CutillasDepartamento de Química Inorgánica, Universidad de Murcia, and Murcia BioHealth Research Institute (IMIB-Arrixaca), 30071, Murcia, Spain.
José RuizDepartamento de Química Inorgánica, Universidad de Murcia, and Murcia BioHealth Research Institute (IMIB-Arrixaca), 30071, Murcia, Spain. jruiz@um.es.ORCID http://orcid.org/0000-0002-0834-337X
Fernando Gandía-HerreroDepartamento de Bioquímica y Biología Molecular A. Unidad Docente de Biología, Facultad de Veterinaria, Universidad de Murcia, 30071, Murcia, Spain. fgandia@um.es.ORCID http://orcid.org/0000-0003-4389-3454
Instituto Murciano de Investigación Biosanitaria · ESUniversidad de Murcia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncosis (from Greek ónkos, meaning "swelling") is a non-apoptotic cell death process related to energy depletion. In contrast to apoptosis, which is the main form of cell death induced by anticancer drugs, oncosis has been relatively less explored but holds potential to overcome drug resistance phenomena. In this study, we report a novel rationally designed mitochondria-targeted iridium(III) complex (OncoIr3) with advantageous properties as a bioimaging agent. OncoIr3 exhibited potent anticancer activity in vitro against cancer cells and displayed low toxicity to normal dividing cells. Flow cytometry and fluorescence-based assays confirmed an apoptosis-independent mechanism involving energy depletion, mitochondrial dysfunction and cellular swelling that matched with the oncotic process. Furthermore, a Caenorhabditis elegans tumoral model was developed to test this compound in vivo, which allowed us to prove a strong oncosis-derived antitumor activity in animals (with a 41% reduction of tumor area). Indeed, OncoIr3 was non-toxic to the nematodes and extended their mean lifespan by 18%. Altogether, these findings might shed new light on the development of anticancer metallodrugs with non-conventional modes of action such as oncosis, which could be of particular interest for the treatment of apoptosis-resistant cancers.

Indexed as

Antineoplastic AgentsNeoplasmsAnimalsApoptosisCell DeathCell Line, TumorIridiumNecrosisAntineoplastic AgentsIridiumAnticancer agentsAntitumor activityCaenorhabditis elegansIridium metallodrugOncosis

Identifiers

PMID36066676
PMCPMC9448686
OpenAlexW4294710620

What OpenQuestion holds

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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 OpenQuestion graph.