Sato Takashi, Shimosato Takeshi, Klinman Dennis M
Department of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Department of Interdisciplinary Genome Sciences and Cell Metabolism, Institute for Biomedical Sciences, Shinshu University, Nagano 399-4598, Japan.
Lung Cancer (Auckl). 2018 Oct 26;9:91-101. doi: 10.2147/LCTT.S156376. eCollection 2018.
"Silica" refers to crystalline particles formed by the combination of silicon with oxygen. Inhalation of silica particles promotes the development of pulmonary fibrosis that over prolonged periods increases the risk of lung cancer. The International Agency for Research on Cancer (IARC) classified crystalline silica as a human carcinogen in 1997. This categorization was questioned due to 1) the absence of dose-response findings, 2) the presence of confounding variables that complicated interpretation of the data and 3) potential selection bias for compensated silicosis. Yet, recent epidemiologic studies strongly support the conclusion that silica exposure increases the risk of lung cancer in humans independent of confounding factors including cigarette smoke. Based on this evidence, the US Occupational Safety and Health Administration (OSHA) lowered the occupational exposure limit for crystalline silica from 0.1 to 0.05 mg/m in 2013. Further supporting the human epidemiologic data, murine models show that chronic silicosis is associated with an increased risk of lung cancer. In animals, the initial inflammation induced by silica exposure is followed by the development of an immunosuppressive microenvironment that supports the growth of lung tumors. This work will review our current knowledge of silica-associated lung cancers, highlighting how recent mechanistic insights support the use of cutting-edge approaches to diagnose and treat silica-related lung cancer.
“二氧化硅”指的是硅与氧结合形成的晶体颗粒。吸入二氧化硅颗粒会促进肺纤维化的发展,长期来看会增加患肺癌的风险。国际癌症研究机构(IARC)在1997年将结晶二氧化硅归类为人类致癌物。这一分类受到质疑,原因如下:1)缺乏剂量反应研究结果;2)存在混淆变量,使数据解读变得复杂;3)在代偿性矽肺方面存在潜在的选择偏倚。然而,近期的流行病学研究有力地支持了以下结论:接触二氧化硅会增加人类患肺癌的风险,且与包括香烟烟雾在内的混杂因素无关。基于这一证据,美国职业安全与健康管理局(OSHA)在2013年将结晶二氧化硅的职业接触限值从0.1毫克/立方米降至0.05毫克/立方米。小鼠模型进一步支持了人类流行病学数据,表明慢性矽肺与患肺癌风险增加有关。在动物身上,二氧化硅暴露引发的初始炎症之后会形成支持肺部肿瘤生长的免疫抑制微环境。本文将综述我们目前对二氧化硅相关肺癌的认识,重点介绍近期的机制见解如何支持采用前沿方法来诊断和治疗二氧化硅相关的肺癌。