Long-fiber carbon nanotubes replicate asbestos-induced mesothelioma with disruption of the tumor suppressor gene Cdkn2a (Ink4a/Arf)

Chernova, Tatyana and Murphy, Fiona A. and Galavotti, Sara and Sun, Xiao Ming and Powley, Ian R. and Grosso, Stefano and Schinwald, Anja and Zacarias-Cabeza, Joaquin and Dudek, Kate M. and Dinsdale, David and Le Quesne, John and Bennett, Jonathan and Nakas, Apostolos and Greaves, Peter and Poland, Craig A. and Donaldson, Ken and Bushell, Martin and Willis, Anne E. and MacFarlane, Marion (2017) Long-fiber carbon nanotubes replicate asbestos-induced mesothelioma with disruption of the tumor suppressor gene Cdkn2a (Ink4a/Arf). Current Biology, 27 (21). 3302-3314.e6. ISSN 0960-9822 (https://doi.org/10.1016/j.cub.2017.09.007)

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Abstract

Mesothelioma is a fatal tumor of the pleura and is strongly associated with asbestos exposure. The molecular mechanisms underlying the long latency period of mesothelioma and driving carcinogenesis are unknown. Moreover, late diagnosis means that mesothelioma research is commonly focused on end-stage disease. Although disruption of the CDKN2A (INK4A/ARF) locus has been reported in end-stage disease, information is lacking on the status of this key tumor suppressor gene in pleural lesions preceding mesothelioma. Manufactured carbon nanotubes (CNTs) are similar to asbestos in terms of their fibrous shape and biopersistent properties and thus may pose an asbestos-like inhalation hazard. Here we show that instillation of either long CNTs or long asbestos fibers into the pleural cavity of mice induces mesothelioma that exhibits common key pro-oncogenic molecular events throughout the latency period of disease progression. Sustained activation of pro-oncogenic signaling pathways, increased proliferation, and oxidative DNA damage form a common molecular signature of long-CNT- and long-asbestos-fiber-induced pathology. We show that hypermethylation of p16/Ink4a and p19/Arf in CNT- and asbestos-induced inflammatory lesions precedes mesothelioma; this results in silencing of Cdkn2a (Ink4a/Arf) and loss of p16 and p19 protein, consistent with epigenetic alterations playing a gatekeeper role in cancer. In end-stage mesothelioma, silencing of p16/Ink4a is sustained and deletion of p19/Arf is detected, recapitulating human disease. This study addresses the long-standing question of which early molecular changes drive carcinogenesis during the long latency period of mesothelioma development and shows that CNT and asbestos pose a similar health hazard. Manufactured carbon nanotubes (CNTs) show structural similarities to asbestos, strongly associated with the fatal tumor mesothelioma. Chernova et al. show that CNTs and asbestos indeed pose similar health hazards and address the long-standing question of which early molecular changes drive carcinogenesis during mesothelioma's long latency period.

ORCID iDs

Chernova, Tatyana, Murphy, Fiona A. ORCID logoORCID: https://orcid.org/0000-0001-7925-0632, Galavotti, Sara, Sun, Xiao Ming, Powley, Ian R., Grosso, Stefano, Schinwald, Anja, Zacarias-Cabeza, Joaquin, Dudek, Kate M., Dinsdale, David, Le Quesne, John, Bennett, Jonathan, Nakas, Apostolos, Greaves, Peter, Poland, Craig A., Donaldson, Ken, Bushell, Martin, Willis, Anne E. and MacFarlane, Marion;
CORE (COnnecting REpositories)