Nishikawa Akiyoshi, Nagano Kasuke, Kojima Hajime, Ogawa Kumiko
Division of Pathology, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki, Kanagawa, 210-9501, Japan; Division of Clinical Pathology, Saiseikai Utsunomiya Hospital, 911-1 Takebayashi, Utsunomiya, Tochigi, 321-0974, Japan.
Nagano Toxicologic-Pathology Consulting, 467-7 Ojiri, Hadano, Kanagawa, 257-0011, Japan.
Regul Toxicol Pharmacol. 2021 Jul;123:104937. doi: 10.1016/j.yrtph.2021.104937. Epub 2021 Apr 24.
According to the International Agency for Research on Cancer classification, formaldehyde is a human carcinogen that targets the nasal cavity. In humans and rats, inhaled formaldehyde is primarily deposited in the nasal cavity mucosa, metabolized to the less toxic formic acid, and finally excreted into the urine or exhaled. Thus, formaldehyde-induced nasal carcinogenicity may be a direct effect of formaldehyde itself, although the underlying mechanisms remain unclear. With regard to cytotoxicity, degeneration and necrosis of nasal respiratory cells occur in rats after short exposure to formaldehyde. Cell proliferation is increased in the damaged cells, suggesting its critical roles both in the early stages and throughout the entire process of nasal carcinogenicity. Hyperplasia, squamous metaplasia, and dysplasia of the damaged epithelium frequently appear as morphological precursor lesions. With regard to genotoxicity, in addition to DNA-protein crosslinks, oxidative DNA damage also occurs in the exposed nasal mucosal cells. Sustained exposure to formaldehyde may cause nasal carcinogenicity through cytotoxicity and auxiliary genotoxicity. In this review, we discuss adverse outcome pathways through which cytotoxicity can lead to carcinogenicity and the development of integrated approaches for testing and assessment for nongenotoxic carcinogens.
根据国际癌症研究机构的分类,甲醛是一种靶向鼻腔的人类致癌物。在人类和大鼠中,吸入的甲醛主要沉积在鼻腔黏膜,代谢为毒性较小的甲酸,最终经尿液排出或呼出。因此,甲醛诱发的鼻腔致癌性可能是甲醛本身的直接作用,尽管其潜在机制尚不清楚。关于细胞毒性,大鼠短期接触甲醛后会出现鼻腔呼吸细胞的变性和坏死。受损细胞中的细胞增殖增加,表明其在鼻腔致癌性的早期阶段和整个过程中都起着关键作用。受损上皮的增生、鳞状化生和发育异常常表现为形态学上的前驱病变。关于遗传毒性,除了DNA-蛋白质交联外,暴露的鼻腔黏膜细胞中还会发生氧化性DNA损伤。持续接触甲醛可能通过细胞毒性和辅助遗传毒性导致鼻腔致癌性。在本综述中,我们讨论了细胞毒性可导致致癌性的不良结局途径以及非遗传毒性致癌物测试和评估综合方法的发展。