Evidence map›Paper›PMID 42610804›Full record

ArticlePhytotherapy research : PTR2026

Piper nigrum Has an Antitumor Effect Through Regulation of the Phosphatidylinositol 3-Kinase Signaling Pathway in a Murine Model of Acute Myeloid Leukemia.

Natalia Murillo, Paola Lasso, Claudia Urueña, Susana Fiorentino

Abstract read
In one paragraph

Article in Phytotherapy research : PTR, 2026. 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
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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

4 authors.

Natalia MurilloGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Departamento de Microbiología, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0001-8484-921X
Paola LassoGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Departamento de Microbiología, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0002-2976-3277
Claudia UrueñaGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Departamento de Microbiología, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0001-5608-3181
Susana FiorentinoGrupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Departamento de Microbiología, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0002-4664-0682

Funding

Instituto Colombiano de Crédito Educativo y Estudios Técnicos en el Exterior FP44842-221-2018Ministerio de Ciencia, Tecnología e Innovación FP44842-221-2018Ministerio de Comercio, Industria y Turismo FP44842-221-2018Ministerio de Educación de la Nación FP44842-221-2018Pontificia Universidad Javeriana FP44842-221-2018World Bank Group FP44842-221-2018
6 · The paper itself

Abstract

The search for safer and more effective therapies for acute myeloid leukemia (AML) has intensified due to low response rates and resistance to current chemotherapy. The aim of this study was to evaluate the antitumor and immunomodulatory effects of Piper nigrum extract in a murine model of AML, with particular emphasis on its ability to modulate the phosphatidylinositol 3-kinase/protein kinase B/mechanistic target of rapamycin (PI3K/AKT/mTOR) signaling pathway. The chemical composition of the extract was characterized using advanced analytical techniques. In vitro assays were performed to evaluate cytotoxic and cytostatic effects, glucose consumption and ROS production, modulation of Gal-9 (galectin 9) and PD-L1 (programmed death-ligand 1), focusing on and relating it to the modulation of the (PI3K/AKT/mTOR) pathway. In vivo studies were performed using mice inoculated with DA-3/ER-GM cells to evaluate hematological parameters, survival, and immune response after P. nigrum treatment. P. nigrum extract demonstrated cytotoxic and cytostatic activity in vitro, characterized by a decrease in cell proliferation and survival possibly associated with modulation of the PI3K/AKT/mTOR pathway. In the murine AML model, treatment significantly reduced circulating blasts, improved hematological parameters, and prolonged survival. In addition, an increase in effector memory CD8

Indexed as

Antineoplastic Agents, PhytogenicLeukemia, Myeloid, AcutePhosphatidylinositol 3-KinasePiper nigrumPlant ExtractsSignal TransductionAnimalsCell Line, TumorCell ProliferationDisease Models, AnimalFemaleMaleMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesAntineoplastic Agents, PhytogenicmTOR protein, mousePhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPlant ExtractsProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinasesacute myeloid leukemia (AML)immunomodulationPI3K/AKT/mTOR pathwayPiper nigrumtumor metabolism

Identifiers

PMID42610804
PMCPMC13636107

What OpenQuestion holds

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Registered trials

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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.