Evidence map›Paper›PMID 39285786›Full record

ArticleJournal of applied toxicology : JAT2025

Flame retardant, hexabromocyclododecane, increases production of pro-inflammatory cytokines, interleukin 1-beta and interleukin 6, in human immune cells.

April Falconer-Turner, Kameron Brooks, Eseoghene Ogaga, Margaret M Whalen

Abstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 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. 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

4 authors.

April Falconer-TurnerDepartment of Biological Sciences, Tennessee State University, Nashville, TN, USA.
Kameron BrooksDepartment of Chemistry, Tennessee State University, Nashville, TN, USA.
Eseoghene OgagaDepartment of Biological Sciences, Tennessee State University, Nashville, TN, USA.
Margaret M WhalenDepartment of Chemistry, Tennessee State University, Nashville, TN, USA.ORCID 0000-0002-1511-9181

Funding

TRAININGU54CA163066 · NCI · TENNESSEE STATE UNIVERSITY · PI MARGARET M WHALEN · 2011 to 2026
$12.8M
U-RISE at Tennessee State UniversityT34GM145334 · NIGMS · TENNESSEE STATE UNIVERSITY · PI WHALEN, MARGARET M · 2022 to 2024
$625k
NCI NIH HHS U54 CA163066NIGMS NIH HHS T34 GM145334
6 · The paper itself

Abstract

Hexabromocyclododecane (HBCD) is an environmental contaminant due to its use as a flame retardant in a variety of applications ranging from building insulation, furniture upholstery, and housing for appliances and electronics. HBCD is found in wildlife, human breastmilk, and serum. Interleukin 1-beta (IL-1β) and interleukin 6 (IL-6) are pro-inflammatory cytokines, whose dysregulation is associated with chronic inflammation and the pathologies that result, such as tumor growth, rheumatoid arthritis, Crohn's disease, and multiple sclerosis. HBCD has been shown to increase the secretion of both IL-1β and IL-6 from human immune cells. However, it is not clear if these increases are due solely to HBCD effects on the secretory process or whether it is stimulating cellular production of IL-1β and IL-6. This study examines if HBCD can increase the production of IL-1β and IL-6 by immune cells by simultaneously assessing secreted levels and cellular levels of these cytokines. Additionally, the mechanisms for any observed changes in production are investigated. Peripheral blood mononuclear cells were exposed to HBCD over a range of concentrations and lengths of exposure. HBCD was found to stimulate IL-1β and IL-6 production after 6 hrs. of exposure and production was sustained and intensified at 24 hrs. This increase in IL-1β and IL-6 production appears to, in part, be a result of increased mRNA expression. Additionally, the MAPK pathways, specifically the p38 and p44/42 pathways, appear to be required for HBCD-induced increases in IL-1β and IL-6 production.

Indexed as

Flame RetardantsHydrocarbons, BrominatedInterleukin-1betaInterleukin-6Leukocytes, MononuclearCells, CulturedHumansRNA, MessengerFlame RetardantshexabromocyclododecaneHydrocarbons, BrominatedIL1B protein, humanIL6 protein, humanInterleukin-1betaInterleukin-6RNA, MessengerHexabromocyclododecaneinterleukin 1βinterleukin 6, MAPKsmRNA

Identifiers

PMID39285786
PMCPMC11748055

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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.