Evidence map›Paper›PMID 40333775›Full record

ArticleMolecules (Basel, Switzerland)2025

Modulation of Tumor Metabolism in Acute Leukemia by Plant-Derived Polymolecular Drugs and Their Effects on Mitochondrial Function.

Cindy Arévalo, Carolina Carlosama, Laura Rojas, Mónica P Cala, Marie-Paule Hamon, Bertrand Friguet, Alfonso Barreto, Susana Fiorentino

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2025. 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

8 authors.

Cindy ArévaloGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0003-4229-0918
Carolina CarlosamaGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Laura RojasGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0001-6584-8123
Mónica P CalaCentro de Metabolómica-MetCore, Universidad de los Andes, Bogotá 111711, Colombia.ORCID 0000-0002-8198-726X
Marie-Paule HamonInstitut de Biologie Paris-Seine, Sorbonne Université, Biological Adaptation and Ageing, 75005 Paris, France.ORCID 0000-0002-3580-8718
Bertrand FriguetInstitut de Biologie Paris-Seine, Sorbonne Université, Biological Adaptation and Ageing, 75005 Paris, France.ORCID 0000-0001-8085-1961
Alfonso BarretoGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Susana FiorentinoGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0002-4664-0682

Funding

Ministerio de Ciencia, Tecnología e Innovación (Colciencias), Ministerio de Educación Nacional, Ministerio de Industria, Comercio y Turismo e ICETEX (792-2017 ªa Convocatoria Ecosistema Científico-- Colombia Científica para la Financiación de Proyectos de Contract No. FP44842-221-2018
6 · The paper itself

Abstract

The analysis of tumor metabolism offers promising opportunities for developing new therapeutic strategies. Plant-derived polymolecular drugs can regulate cellular metabolism, making them potential candidates for treatment. This study examined the metabolic effects of plant-derived polymolecular drugs-P2Et, Anamu-SC, and Esperanza-on leukemic cell lines (lymphoid and myeloid types) and primary leukemic blasts. The metabolic analysis included oxidative status, glucose consumption, extracellular acidification, oxygen consumption, mitochondrial dynamics, and untargeted metabolomics. Additionally, the effect of co-treatment with conventional chemotherapeutic drugs was investigated. Results showed that P2Et and Anamu-SC reduced the viability and proliferation of all tumor cell lines, exhibiting antioxidant effects. Anamu-SC decreased reactive oxygen species levels in lymphoid tumor cells. Mitochondrial activity was selectively affected by the plant-derived polymolecular drugs, with Anamu-SC and Esperanza causing more significant, potentially reversible damage compared to P2Et. Anamu-SC and Esperanza increased levels of phosphatidylcholines and carnitines. The co-administration of plant-derived polymolecular drugs with chemotherapeutics improved the cytostatic efficacy of cytarabine. In conclusion, this research highlights the promising pharmacological activity of Anamu-SC and Esperanza as mitocans for the treatment of acute leukemia. The study emphasizes the practical significance of combining plant-derived polymolecular drugs with conventional chemotherapeutics to enhance their cytostatic efficacy.

Indexed as

Antineoplastic Agents, PhytogenicLeukemiaMitochondriaPlant ExtractsCell Line, TumorCell ProliferationCell SurvivalHumansMetabolomicsReactive Oxygen SpeciesAntineoplastic Agents, PhytogenicPlant ExtractsReactive Oxygen Speciesacute leukemiachemotherapymetabolismmitocansplant-derived polymolecular drugs

Identifiers

PMID40333775
PMCPMC12029889

What OpenQuestion holds

Textmetadata
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.