Zeolites ameliorate asbestos toxicity in a transgenic model of malignant mesothelioma

被引:4
|
作者
Fan, Xiyong [1 ]
McLaughlin, Chris [1 ]
Robinson, Cleo [2 ,3 ]
Ravasini, Jason [1 ]
Schelch, Karin [4 ,5 ,6 ]
Johnson, Thomas [4 ,5 ]
Zandwijk, Nico [4 ]
Reid, Glen [1 ,4 ,5 ,7 ]
George, Anthony M. [1 ]
机构
[1] Univ Technol Sydney, Sch Life Sci, POB 123, Broadway, NSW 2007, Australia
[2] Univ Western Australia M503, Sch Biomed Sci, Crawley, WA, Australia
[3] QEII Med Ctr, Mol Anat Pathol, PathWest Lab Med, Nedlands, WA, Australia
[4] Univ Sydney, Asbestos Dis Res Inst, Sydney, NSW, Australia
[5] Univ Sydney, Fac Med, Sydney, NSW, Australia
[6] Med Univ Vienna, Dept Med 1, Inst Canc Res, Vienna, Austria
[7] Univ Otago, Dept Pathol, Dunedin, New Zealand
关键词
asbestos; Mesothelioma; mouse model; zeolites; T-ANTIGEN; IRON; CLINOPTILOLITE; CELLS; SV40; FIBERS; MOUSE; TRANSFORMATION; PATHOGENESIS; MACROPHAGES;
D O I
10.1096/fba.2019-00040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malignant mesothelioma (MM) is an almost invariably fatal cancer caused by asbestos exposure. The toxicity of asbestos fibers is related to their physicochemical properties and the generation of free radicals. We set up a pilot study to investigate the potential of the zeolite clinoptilolite to counteract the asbestos carcinogenesis by preventing the generation of reactive nitrogen and oxygen radicals. In cell culture experiments, clinoptilolite prevented asbestos-induced cell death, reactive oxygen species production, DNA degradation, and overexpression of genes known to be upregulated by asbestos. In an asbestos-induced transgenic mouse model of MM, mice were injected intraperitoneal injections with blue asbestos, with or without clinoptilolite, and monitored for 30 weeks. By the end of the trial all 13 mice injected with asbestos alone had reached humane end points, whereas only 7 of 29 mice receiving crocidolite and clinoptilolite reached a similar stage of disease. Post-mortem examination revealed pinpoint mesothelioma-like tumors in affected mice, and the absence of tumor formation in surviving mice. Interestingly, the macrophage clearance system, which was largely suppressed in asbestos-treated mice, exhibited evidence of increased phagocytosis in mice treated with asbestos and clinoptilolite. Our study suggests that inhibiting the asbestos-induced generation of reactive oxygen species and stimulating the macrophage system may represent a pathway to amelioration of asbestos-induced toxicity. Additional studies are warranted to explore the underlying mechanisms responsible for our observations.
引用
收藏
页码:550 / 560
页数:11
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