Evidence map›Paper›PMID 41160187›Full record

ArticleMedical oncology (Northwood, London, England)2025

Exploring novel therapeutic strategies: Static Magnetic Fields in combination with doxorubicin induce ROS and apoptosis in acute lymphoblastic leukemia cells.

Amirsalar Nikkhah Bahrami, Mohammad Hadi Sadeghian, Nader Vazifeh Shiran

Abstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 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

3 authors.

Amirsalar Nikkhah BahramiDepartment of Hematology, Faculty of Medicine, Mashhad University of Medical Science, Mashhad, Iran.ORCID http://orcid.org/0009-0001-9410-4585
Mohammad Hadi SadeghianDepartment of Hematology and Blood Banking, Cancer Molecular Pathology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID http://orcid.org/0000-0003-3158-6983
Nader Vazifeh ShiranDepartment of Hematology and Blood Banking, Paramedical Faculty, Shahid Beheshti University of Medical Sciences, Tehran, Iran. nadershirani@yahoo.com.ORCID http://orcid.org/0000-0003-0438-4438

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphoblastic leukemia (ALL), primarily affecting children, is a rare malignancy. This study explores the use of alternative therapies such as Static Magnetic Fields (SMF) and Doxorubicin (Dox) as a novel therapeutic strategy for ALL NALM-6 cells. Viability, apoptosis, cell cycle, ROS, and gene expression were assessed using Trypan blue, MTT, flow cytometry, and qRT-PCR. SMF significantly reduced NALM-6 viability and metabolic activity, increased apoptosis and ROS, and altered gene expression related to apoptosis, ROS, cell cycle, and autophagy. Co-treatment with SMF and Dox enhanced these effects compared to single treatments (p ≤ .05), with no cytotoxicity to normal PBMCs or L929 cells. SMF alone or with Dox induces ROS-mediated apoptosis and autophagy inhibition, suggesting a potential complementary therapy, though further research is needed.

Indexed as

Antibiotics, AntineoplasticApoptosisDoxorubicinMagnetic FieldsPrecursor Cell Lymphoblastic Leukemia-LymphomaReactive Oxygen SpeciesAutophagyCell Line, TumorCell SurvivalCombined Modality TherapyHumansAntibiotics, AntineoplasticDoxorubicinReactive Oxygen SpeciesAcute lymphoblastic leukemiaApoptosisAutophagyDoxorubicinLeukemia cell line (NALM-6)Reactive oxygen speciesStatic Magnetic Field therapy

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.