Evidence map›Paper›PMID 39937830›Full record

ArticlePloS one2025

Characterization of the atypical antipsychotic drug aripiprazole cytotoxicity in the neutrophil model cell line HL-60.

Courtney A Swain, Emily J Robbs, Lindsay Verma, Heaven Brandt, Alexandra L Seppaenen, Peter J Cavnar

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Harnessing pyroptosis to restrain melanoma through aripiprazole.Apoptosis : an international journal on programmed cell death · 2026
    Article
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

6 authors.

Courtney A SwainDepartment of Pathology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.ORCID https://orcid.org/0000-0002-5671-0218
Emily J RobbsDepartment of Biology, University of West Florida, Pensacola, Florida, United States of America.
Lindsay VermaDepartment of Biology, University of West Florida, Pensacola, Florida, United States of America.
Heaven BrandtDepartment of Biology, University of West Florida, Pensacola, Florida, United States of America.ORCID https://orcid.org/0009-0001-1419-7567
Alexandra L SeppaenenDepartment of Biology, University of West Florida, Pensacola, Florida, United States of America.
Peter J CavnarDepartment of Biology, University of West Florida, Pensacola, Florida, United States of America.ORCID https://orcid.org/0000-0002-4038-4972

Funding

MARC at University of West FloridaT34GM110517 · NIGMS · UNIVERSITY OF WEST FLORIDA · PI CAVNAR, PETER J., MOLEK, KAREN SINCLAIR · 2014 to 2023
$2.6M
NIGMS NIH HHS T34 GM110517
6 · The paper itself

Abstract

Atypical antipsychotics are widely used for the treatment of mental and behavioral disorders such as bipolar disorder, obsessive-compulsive disorder, and schizophrenia. However, these drugs can occasionally induce neutropenia or agranulocytosis, characterized by a significant reduction in circulating neutrophils, the primary white blood cells responsible for immune responses. This drug-induced neutropenia poses a considerable risk of life-threatening infections. However, the precise mechanism by which atypical antipsychotics induce neutropenia remains unclear. This study investigates the effects of four atypical antipsychotics, namely - aripiprazole, clozapine, olanzapine, and quetiapine - on the human neutrophil model cell line HL-60. These drugs, which modulate dopamine receptor signaling alongside other mechanisms, were analyzed for their effects. Among these, aripiprazole - but not the others - uniquely induced apoptosis in a dose-dependent manner, accompanied by an increased expression of pro-apoptotic genes - BAK, BCL10, and caspase-3. Moreover, our study elucidates that while differentiated HL-60 cells express D1-like and D2-like dopamine receptors, aripiprazole's cytotoxic effects appear to operate through dopamine-independent pathways and significantly reduce phosphorylated Src family kinase levels. Our results align with previous studies suggesting that aripiprazole exhibits cytotoxic properties in neutrophils. Nevertheless, further investigations are warranted to investigate the mechanisms underlying aripiprazole-induced apoptosis in neutrophils.

Indexed as

Antipsychotic AgentsAripiprazoleNeutrophilsApoptosisBenzodiazepinesCaspase 3ClozapineHL-60 CellsHumansOlanzapineQuetiapine FumarateSignal Transductionsrc-Family KinasesAntipsychotic AgentsAripiprazoleBenzodiazepinesCaspase 3ClozapineOlanzapineQuetiapine Fumaratesrc-Family Kinases

Identifiers

PMID39937830
PMCPMC11819542

What Socratic holds

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LicenceCC BY
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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 Socratic graph.