Evidence map›Paper›PMID 41310828›Full record

ArticleParticle and fibre toxicology2025

Inhalation toxicity of arsenic-containing mine dust in an air-liquid interface bronchial epithelial model.

Xiaoli Ji, Yanping Li, Shuyi Gu, Zhen Min, Daoyuan Sun, Ziren Zhang, Wenkang Jiang, Jingbo Zhang

Abstract read
In one paragraph

Article in Particle and fibre toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Xiaoli Ji *Department of Occupational Disease, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China.
Yanping Li *Department of Respiratory Medicine, Honghe Prefecture Third People's Hospital, Gejiu, 661000, Yunnan, China.
Shuyi Gu *Pharmacology and Toxicology Department, Shanghai Institute for Food and Drug Control, Shanghai, 201203, China.
Zhen MinDepartment of Occupational Disease, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China.
Daoyuan SunDepartment of Occupational Disease, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China.
Ziren ZhangDepartment of Occupational Disease, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China.
Wenkang JiangDepartment of Intensive Care Medicine, Honghe Prefecture Third People's Hospital, Gejiu, 661000, Yunnan, China. 305383197@qq.com.
Jingbo ZhangDepartment of Occupational Disease, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, China. 13585506860@163.com.

Funding

Cooperation Project of Science and Technology Commission of Shanghai Municipality, China 23015820200Domestic National Key Research and Development Program on Prevention and Control of Common and Frequent Diseases 2023YFC2509300Major Science and Technology Special Project of Yunnan Province 202402AA310076Shanghai 3-year Public Health Action Plan, Shanghai, China GWVI-11.1-37Shanghai Pulmonary Hospital development Fund. 202409-4337
6 · The paper itself

Abstract

backgroundTin mine dust (MD), a by-product of tin mining and rock drilling, is a significant contributor to miners' pneumoconiosis. This aerosolized dust is a complex mixture of mineral components, including potentially toxic heavy metals such as arsenic, which may contribute to the development of pneumoconiosis and lung cancer. This study investigates the inhalation toxicity of tin MD samples on pulmonary cells using an Air-Liquid Interface (ALI) exposure model.

resultsMD-A was characterized by high arsenic content, exceeding 30%. In contrast, the elemental composition of MD-B and MD-C was predominantly composed of calcium, magnesium, and aluminum. In the toxicity study, key toxicological endpoints (cell viability, cytotoxicity, pro-inflammatory markers, and cell barrier function) were systematically assessed, and real-time monitoring of the cell-delivered MD particles (MD-A, MD-B, MD-C, and silica) concentrations was achieved using QCM. MD-A significantly enhanced the proliferation ability of 16HBE and Calu-3 cells compared to other particulate matters, indicating arsenic-containing MD promotes cell proliferation. MD-A resulted in an increase in IL-1β mRNA expression in 16HBE cells; elevations in IL-1β, IL-6, IL-8, TNF-α, and CCL2 mRNA were observed in Calu-3 cells. Additionally, treatment with four different particles significantly increased the mRNA expression of MUC5AC in both cell types. Immunofluorescence staining demonstrated alterations in the typical morphology of epithelial cells exposed to arsenic-containing MD and silica particles. In this study, it was shown that four types of particles delivered via suspension to the same in vitro model can induce differing levels of cytotoxicity and proinflammatory responses. The differences in results underscore the specific effects of the inherent physicochemical attributes of particles on biological interactions.

conclusionsUnder identical particle size conditions, in vitro studies on inhalation toxicity reveal that the chemical composition of particulate matter causes varying degrees of toxic damage to cells. This study utilizes an advanced in vitro method to assess the inhalation hazards of tin MD particles by integrating the ALICE system. The chemical complexity of tin MD, particularly its significant arsenic content, requires special attention and thorough evaluation.

Indexed as

Air Pollutants, OccupationalArsenicBronchiDustEpithelial CellsInhalation ExposureMiningTinCell LineCell ProliferationCell SurvivalCytokinesHumansParticle SizeAir Pollutants, OccupationalArsenicCytokinesDustTinAir-liquid interfaceBronchial epithelial cellInhalation toxicityIn vitroTin mine dust

Identifiers

PMID41310828
PMCPMC12659116

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.