Contribution of toxicological pathology to occupational health: lung carcinogenicity of fibrous and particulate substances in rats.

IF 0.9 4区 医学 Q4 PATHOLOGY Journal of Toxicologic Pathology Pub Date : 2023-04-01 DOI:10.1293/tox.2022-0086
Shoji Fukushima, Tatsuya Kasai, Hideki Senoh, Yumi Umeda, Takashi Mine, Toshiaki Sasaki, Hitomi Kondo, Michiharu Matsumoto, Shigetoshi Aiso
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引用次数: 1

Abstract

In this review, we focus on the rat pulmonary carcinogenicity of two solid substances, fibrous multi-walled carbon nanotube (MWCNT) and particulate indium tin oxide (ITO). Inhalation exposure to MWNT-7, a type of MWCNTs, and ITO induced lung carcinogenicity in both male and female rats. Toxicity to the alveolar epithelium is induced by macrophages undergoing frustrated phagocytosis or frustrated degradation of engulfed particles (referred to as frustrated macrophages). Melted macrophage contents contribute significantly to development of hyperplasia of the alveolar epithelium, which eventually results in the induction of lung carcinoma. MWNT-7 and ITO induce secondary genotoxicity; consequently, a no-observed-adverse-effect level can be applied to these materials rather than benchmark doses that are used for non-threshold carcinogens. Thus, establishing occupational exposure limit values for MWNT-7 and ITO based on the existence of a carcinogenic threshold is reasonable.

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毒理学病理学对职业健康的贡献:纤维和颗粒物质在大鼠中的肺癌致癌性。
本文综述了纤维多壁碳纳米管(MWCNT)和颗粒氧化铟锡(ITO)两种固体物质对大鼠肺致癌性的影响。吸入暴露于MWNT-7(一种MWCNTs)和ITO可诱导雄性和雌性大鼠的肺癌致癌性。对肺泡上皮的毒性是由吞噬受阻或被吞噬颗粒降解受阻的巨噬细胞(称为受阻巨噬细胞)诱导的。融化的巨噬细胞内容物显著促进肺泡上皮增生的发展,最终导致肺癌的诱导。MWNT-7和ITO诱导继发性遗传毒性;因此,可以对这些材料采用未观察到的不良影响水平,而不是对非阈值致癌物使用的基准剂量。因此,基于致癌阈值的存在来确定MWNT-7和ITO的职业暴露极限值是合理的。
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来源期刊
Journal of Toxicologic Pathology
Journal of Toxicologic Pathology PATHOLOGY-TOXICOLOGY
CiteScore
2.10
自引率
16.70%
发文量
22
审稿时长
>12 weeks
期刊介绍: JTP is a scientific journal that publishes original studies in the field of toxicological pathology and in a wide variety of other related fields. The main scope of the journal is listed below. Administrative Opinions of Policymakers and Regulatory Agencies Adverse Events Carcinogenesis Data of A Predominantly Negative Nature Drug-Induced Hematologic Toxicity Embryological Pathology High Throughput Pathology Historical Data of Experimental Animals Immunohistochemical Analysis Molecular Pathology Nomenclature of Lesions Non-mammal Toxicity Study Result or Lesion Induced by Chemicals of Which Names Hidden on Account of the Authors Technology and Methodology Related to Toxicological Pathology Tumor Pathology; Neoplasia and Hyperplasia Ultrastructural Analysis Use of Animal Models.
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