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吸入 MWCNT 可强力促进肺部肿瘤生长。

Potent lung tumor promotion by inhaled MWCNT.

机构信息

Pathology and Physiology Research Branch, Health Effects Laboratory Division, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, Morgantown, WV, USA.

Charles River Laboratories, Inc, Durham, NC, USA.

出版信息

Nanotoxicology. 2024 Feb;18(1):69-86. doi: 10.1080/17435390.2024.2314473. Epub 2024 Feb 29.

Abstract

In the lung, carcinogenesis is a multi-stage process that includes initiation by a genotoxic agent, promotion that expands the population of cells with damaged DNA to form a tumor, and progression from benign to malignant neoplasms. We have previously shown that Mitsui-7, a long and rigid multi-walled carbon nanotube (MWCNT), promotes pulmonary carcinogenesis in a mouse model. To investigate the potential exposure threshold and dose-response for tumor promotion by this MWCNT, 3-methylcholanthrene (MC) initiated (10 μg/g, i.p., once) or vehicle (corn oil) treated B6C3F1 mice were exposed by inhalation to filtered air or MWCNT (5 mg/m) for 5 h/day for 0, 2, 5, or 10 days and were followed for 17 months post-exposure for evidence of lung tumors. Pulmonary neoplasia incidence in MC-initiated mice significantly increased with each MWCNT exposure duration. Exposure to either MC or MWCNT alone did not affect pulmonary neoplasia incidence compared with vehicle controls. Lung tumor multiplicity in MC-initiated mice also significantly increased with each MWCNT exposure duration. Thus, a significantly higher lung tumor multiplicity was observed after a 10-day MWCNT exposure than following a 2-day exposure. Both bronchioloalveolar adenoma and bronchioloalveolar adenocarcinoma multiplicity in MC-initiated mice were significantly increased following 5- and 10-day MWCNT exposure, while a 2-day MWCNT exposure in MC-initiated mice significantly increased the multiplicity of adenomas but not adenocarcinomas. In this study, even the lowest MWCNT exposure promoted lung tumors in MC-initiated mice. Our findings indicate that exposure to this MWCNT strongly promotes pulmonary carcinogenesis.

摘要

在肺部,癌变是一个多阶段的过程,包括遗传毒性物质的引发、促进,即扩大具有受损 DNA 的细胞群体以形成肿瘤,以及从良性到恶性肿瘤的进展。我们之前已经表明,三井-7,一种长而刚性的多壁碳纳米管(MWCNT),在小鼠模型中促进了肺癌的发生。为了研究这种 MWCNT 促进肿瘤形成的潜在暴露阈值和剂量反应,用 3-甲基胆蒽(MC)(10μg/g,腹腔内,一次)或载体(玉米油)预处理 B6C3F1 小鼠,通过吸入过滤空气或 MWCNT(5mg/m)进行暴露,每天 5 小时,持续 0、2、5 或 10 天,并在暴露后 17 个月内进行随访,以观察肺部肿瘤的证据。MC 引发的小鼠肺部肿瘤发生率随着 MWCNT 暴露时间的延长而显著增加。与载体对照相比,单独暴露于 MC 或 MWCNT 并不影响肺部肿瘤发生率。MC 引发的小鼠肺部肿瘤多发性也随着 MWCNT 暴露时间的延长而显著增加。因此,与 2 天暴露相比,在 10 天 MWCNT 暴露后观察到明显更高的肺部肿瘤多发性。MC 引发的小鼠的细支气管肺泡腺瘤和细支气管肺泡腺癌多发性也随着 5 天和 10 天 MWCNT 暴露而显著增加,而 2 天 MWCNT 暴露在 MC 引发的小鼠中显著增加了腺瘤的多发性,但不增加腺癌的多发性。在这项研究中,即使是最低的 MWCNT 暴露也促进了 MC 引发的小鼠的肺部肿瘤。我们的研究结果表明,暴露于这种 MWCNT 强烈促进了肺部癌变。

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