Evidence map›Paper›PMID 32580382›Full record

ArticlePolymers2020

Toxic Effects of Urethane Dimethacrylate on Macrophages Through Caspase Activation, Mitochondrial Dysfunction, and Reactive Oxygen Species Generation.

Chih-Yang Chang, Chen-Yu Chiang, Yun-Wei Chiang, Min-Wei Lee, Chien-Ying Lee, Hung-Yi Chen, Hui-Wen Lin, Yu-Hsiang Kuan

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% of its field
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  10. Motion artifact-controlled micro-brain sensors between hair follicles for persistent augmented reality brain-computer interfaces.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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 at 5 institutions in 1 country.

Chih-Yang ChangDivision of Pediatric Surgery, Department of Pediatrics, Ditmanson Medical Foundation Chia- Yi Christian Hospital, 600 Chia- Yi City, Taiwan.
Chen-Yu ChiangDepartment of Veterinary Medicine, National Chung-Hsing University, 402 Taichung, Taiwan.
Yun-Wei ChiangDepartment of life sciences, National Chung-Hsing University, 402 Taichung, Taiwan.
Min-Wei LeeA Graduate Institute of Microbiology and Public Health, National Chung Hsing University, 402 Taichung, Taiwan.
Chien-Ying LeeDepartment of Pharmacology, School of Medicine, Chung Shan Medical University, 402 Taichung, Taiwan.
Hung-Yi ChenSchool of Pharmacy, China Medical University, 404 Taichung, Taiwan.
Hui-Wen LinDepartment of Optometry, Asia University, 413 Taichung, Taiwan.
Yu-Hsiang KuanDepartment of Pharmacology, School of Medicine, Chung Shan Medical University, 402 Taichung, Taiwan.
National Chung Hsing University · TWChung Shan Medical University Hospital · TWAsia University · TWChia-Yi Christian Hospital · TWChina Medical University · TW

Funding

Ministry of Science and Technology of the Republic of China MOST 106-232-B-040-022-MY3
6 · The paper itself

Abstract

Urethane dimethacrylate (UDMA) is a dimethacrylate-based resin monomer that can react with other related monomers and inorganic particles, causing hydrophobic polymerization through cross-linking upon light activation. UDMA polymers are commonly used for the reconstruction and reinforcement of teeth and bones. UDMA can become unbound and be released from light-cured polymer resins. Thus far, no evidence exists on the toxic effects of UDMA and its related working mechanisms for macrophages. Therefore, in the present study, we investigated the cytotoxicity, mode of cell death, DNA damage, caspase activities, mitochondrial dysfunction, and reactive oxygen species (ROS) generation in RAW264.7 macrophages treated with UDMA using the lactate dehydrogenase (LDH) assay kit, Annexin V-FITC and PI assays, micronucleus formation and comet assay, caspase fluorometric assay, JC-1 assay, and 2',7'-dichlorofluorescin diacetate (DCFH-DA) assay, respectively. Our results show that UDMA induced cytotoxicity; apoptosis and necrosis; genotoxicity, which is also called DNA damage; increased caspase-3, -8, and -9 activities; mitochondrial dysfunction; and intracellular ROS generation in a concentration-dependent manner in RAW264.7 macrophages. Thus, based on the observed inhibited concentration parallel trends, we concluded that UDMA induces toxic effects in macrophages. Furthermore, UDMA-induced intracellular ROS generation, cytotoxicity, and DNA damage were reduced by N-acetyl-L-cysteine.

Indexed as

apoptosiscaspase activationgenotoxicitymacrophageROS generationUDMA

Identifiers

PMID32580382
PMCPMC7361960
OpenAlexW3035850100

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.