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吸入铜焊接烟尘后,小鼠肺部肿瘤体积缩小,肿瘤促进作用缺失。

Absence of lung tumor promotion with reduced tumor size in mice after inhalation of copper welding fumes.

机构信息

Health Effects Laboratory Division, National Institute for Occupational Safety and Health, 1000 Frederick Lane, Morgantown, WV 26508, United States.

Department of Dermatology, University of Pittsburgh Medical Center, 3708 Fifth Avenue Suite 500.68, Pittsburgh, PA 15213, United States.

出版信息

Carcinogenesis. 2024 Sep 11;45(9):630-641. doi: 10.1093/carcin/bgae048.

Abstract

Welding fumes are a Group 1 (carcinogenic to humans) carcinogen as classified by the International Agency for Research on Cancer. The process of welding creates inhalable fumes rich in iron (Fe) that may also contain known carcinogenic metals such as chromium (Cr) and nickel (Ni). Epidemiological evidence has shown that both mild steel (Fe-rich) and stainless steel (Fe-rich + Cr + Ni) welding fume exposure increases lung cancer risk, and experimental animal data support these findings. Copper-nickel (CuNi) welding processes have not been investigated in the context of lung cancer. Cu is intriguing, however, given the role of Cu in carcinogenesis and cancer therapeutics. This study examines the potential for a CuNi fume to induce mechanistic key characteristics of carcinogenesis in vitro and to promote lung tumorigenesis, using a two-stage mouse bioassay, in vivo. Male A/J mice, initiated with 3-methylcholanthrene (MCA; 10 µg/g), were exposed to CuNi fumes or air by whole-body inhalation for 9 weeks (low deposition-LD and high deposition-HD) and then sacrificed at 30 weeks. In BEAS-2B cells, the CuNi fume-induced micronuclei and caused DNA damage as measured by γ-H2AX. The fume exhibited high reactivity and a dose-response in cytotoxicity and oxidative stress. In vivo, MCA/CuNi HD and LD significantly decreased lung tumor size and adenomas. MCA/CuNi HD exposure significantly decreased gross-evaluated tumor number. In summary, the CuNi fume in vitro exhibited characteristics of a carcinogen, but in vivo, the exposure resulted in smaller tumors, fewer adenomas, less hyperplasia severity, and with HD exposure, less overall lung lesions/tumors.

摘要

焊接烟尘被国际癌症研究机构(IARC)归类为 1 类(对人类致癌)致癌物。焊接过程会产生可吸入的烟尘,其中富含铁(Fe),还可能含有已知的致癌金属,如铬(Cr)和镍(Ni)。流行病学证据表明,无论是低碳钢(富铁)还是不锈钢(富铁+Cr+Ni)焊接烟尘暴露都会增加肺癌风险,并且实验动物数据支持这些发现。铜镍(CuNi)焊接工艺尚未在肺癌背景下进行研究。然而,鉴于铜在致癌作用和癌症治疗中的作用,Cu 很有趣。本研究使用两段式小鼠生物测定法,在体内研究了 CuNi 烟尘是否具有诱导体外致癌发生的机制关键特征,并促进肺肿瘤发生的潜力。雄性 A/J 小鼠经 3-甲基胆蒽(MCA;10 µg/g)引发后,通过全身吸入暴露于 CuNi 烟尘或空气 9 周(低沉积-LD 和高沉积-HD),然后在 30 周时处死。在 BEAS-2B 细胞中,CuNi 烟尘诱导微核形成,并通过 γ-H2AX 测量引起 DNA 损伤。烟尘表现出高反应性和细胞毒性及氧化应激的剂量反应性。在体内,MCA/CuNi HD 和 LD 显著降低了肺肿瘤大小和腺瘤。MCA/CuNi HD 暴露显著降低了总评估肿瘤数量。总之,CuNi 烟尘在体外表现出致癌物的特征,但在体内暴露导致肿瘤更小,腺瘤更少,增生严重程度更低,并且 HD 暴露时,肺部病变/肿瘤总数更少。

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