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      Multiwalled carbon nanotubes intratracheally instilled into the rat lung induce development of pleural malignant mesothelioma and lung tumors

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          Abstract

          Multiwalled carbon nanotubes (MWCNT) have a fibrous structure and physical properties similar to asbestos and have been shown to induce malignant mesothelioma of the peritoneum after injection into the scrotum or peritoneal cavity in rats and mice. For human cancer risk assessment, however, data after administration of MWCNT via the airway, the exposure route that is most relevant to humans, is required. The present study was undertaken to investigate the carcinogenicity of MWCNT‐N (NIKKISO) after administration to the rat lung. MWCNT‐N was fractionated by passing it through a sieve with a pore size of 25 μm. The average lengths of the MWCNT were 4.2 μm before filtration and 2.6 μm in the flow‐through fraction; the length of the retained MWCNT could not be determined. For the present study, 10‐week‐old F344/Crj male rats were divided into five groups: no treatment, vehicle control, MWCNT‐N before filtration, MWCNT‐N flow‐through and MWCNT‐N retained groups. Administration was by the trans‐tracheal intrapulmonary spraying (TIPS) method. Rats were administered a total of 1 mg/rat during the initial 2 weeks of the experiment and then observed up to 109 weeks. The incidences of malignant mesothelioma and lung tumors (bronchiolo‐alveolar adenomas and carcinomas) were 6/38 and 14/38, respectively, in the three groups administered MWCNT and 0/28 and 0/28, respectively, in the control groups. All malignant mesotheliomas were localized in the pericardial pleural cavity. The sieve fractions did not have a significant effect on tumor incidence. In conclusion, administration of MWCNT to the lung in the rat induces malignant mesothelioma and lung tumors.

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          Inflammation and cancer: advances and new agents.

          Tumour-promoting inflammation is considered one of the enabling characteristics of cancer development. Chronic inflammatory disease increases the risk of some cancers, and strong epidemiological evidence exists that NSAIDs, particularly aspirin, are powerful chemopreventive agents. Tumour microenvironments contain many different inflammatory cells and mediators; targeting these factors in genetic, transplantable and inducible murine models of cancer substantially reduces the development, growth and spread of disease. Thus, this complex network of inflammation offers targets for prevention and treatment of malignant disease. Much potential exists in this area for novel cancer prevention and treatment strategies, although clinical research to support targeting of cancer-related inflammation and innate immunity in patients with advanced-stage cancer remains in its infancy. Following the initial successes of immunotherapies that modulate the adaptive immune system, we assert that inflammation and innate immunity are important targets in patients with cancer on the basis of extensive preclinical and epidemiological data. The adaptive immune response is heavily dependent on innate immunity, therefore, inhibiting some of the tumour-promoting immunosuppressive actions of the innate immune system might enhance the potential of immunotherapies that activate a nascent antitumour response.
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            Asbestos, carbon nanotubes and the pleural mesothelium: a review of the hypothesis regarding the role of long fibre retention in the parietal pleura, inflammation and mesothelioma

            The unique hazard posed to the pleural mesothelium by asbestos has engendered concern in potential for a similar risk from high aspect ratio nanoparticles (HARN) such as carbon nanotubes. In the course of studying the potential impact of HARN on the pleura we have utilised the existing hypothesis regarding the role of the parietal pleura in the response to long fibres. This review seeks to synthesise our new data with multi-walled carbon nanotubes (CNT) with that hypothesis for the behaviour of long fibres in the lung and their retention in the parietal pleura leading to the initiation of inflammation and pleural pathology such as mesothelioma. We describe evidence that a fraction of all deposited particles reach the pleura and that a mechanism of particle clearance from the pleura exits, through stomata in the parietal pleura. We suggest that these stomata are the site of retention of long fibres which cannot negotiate them leading to inflammation and pleural pathology including mesothelioma. We cite thoracoscopic data to support the contention, as would be anticipated from the preceding, that the parietal pleura is the site of origin of pleural mesothelioma. This mechanism, if it finds support, has important implications for future research into the mesothelioma hazard from HARN and also for our current view of the origins of asbestos-initiated pleural mesothelioma and the common use of lung parenchymal asbestos fibre burden as a correlate of this tumour, which actually arises in the parietal pleura.
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              Mouse pulmonary dose- and time course-responses induced by exposure to multi-walled carbon nanotubes.

              Carbon nanotubes (CNT) come in a variety of types, but one of the most common forms is multi-walled carbon nanotubes (MWCNT). MWCNT have potential applications in many diverse commercial processes, and thus human exposures are considered to be likely. In order to investigate the pulmonary toxicity of MWCNT, we conducted an in vivo dose-response and time course study of MWCNT in mice in order to assess their ability to induce pulmonary inflammation, damage, and fibrosis using doses that approximate estimated human occupational exposures. MWCNT were dispersed in dispersion medium (DM) and male C57BL/6J mice (7 weeks old) received either DM (vehicle control), 10, 20, 40 or 80mug MWCNT by aspiration exposure. At 1, 7, 28 and 56 days post-exposure, MWCNT-induced pulmonary toxicity was investigated. Bronchoalveolar lavage (BAL) studies determined pulmonary inflammation and damage was dose-dependent and peaked at 7 days post-exposure. By 56 days post-exposure, pulmonary inflammation and damage markers were returning to control levels, except for the 40mug MWCNT dose, which was still significantly higher than vehicle control. Histopathological studies determined that MWCNT exposure caused rapid development of pulmonary fibrosis by 7 days post-exposure, that granulomatous inflammation persisted throughout the 56-day post-exposure period, and also demonstrated that MWCNT can reach the pleura after pulmonary exposure. In summary, the data reported here indicate that MWCNT exposure rapidly produces significant adverse health outcomes in the lung. Furthermore, the observation that MWCNT reach the pleura after aspiration exposure indicates that more extensive investigations are needed to fully assess if pleural penetration results in any adverse health outcomes.
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                Author and article information

                Journal
                Cancer Sci
                Cancer Sci
                10.1111/(ISSN)1349-7006
                CAS
                Cancer Science
                John Wiley and Sons Inc. (Hoboken )
                1347-9032
                1349-7006
                23 June 2016
                July 2016
                : 107
                : 7 ( doiID: 10.1111/cas.2016.107.issue-7 )
                : 924-935
                Affiliations
                [ 1 ] Department of Molecular ToxicologyNagoya City University Graduate School of Medical Sciences NagoyaJapan
                [ 2 ] Department of Experimental Pathology and Tumor BiologyNagoya City University Graduate School of Medical Sciences NagoyaJapan
                [ 3 ] Nanotoxicology ProjectNagoya City University NagoyaJapan
                [ 4 ] Forensic Medicine and Toxicology Faculty of Veterinary MedicineBeni‐Suef University Beni‐SuefEgypt
                [ 5 ] Japan Industrial Safety and Health AssociationJapan Bioassay Research Center KanagawaJapan
                [ 6 ]National Center for Child Health and Development TokyoJapan
                [ 7 ] Institute of Carbon Science and TechnologyShinshu University Nagano CityJapan
                [ 8 ] Division of Risk Assessment National Institute of Health SciencesAkihiko Hirose TokyoJapan
                [ 9 ] Division of Cellular and Molecular ToxicologyNational Institute of Health Sciences TokyoJapan
                [ 10 ] Department of Pharmaceutical and Environmental SciencesTokyo Metropolitan Institute of Public Health TokyoJapan
                [ 11 ] Department of Immunology College of Basic Medical SciencesAnhui Medical University HefeiChina
                Author notes
                [*] [* ] Correspondence

                Xu Jiegou, Department of Immunology, College of Basic Medical Sciences, Anhui Medical University, Meishan Road 81, Hefei 230032, China.

                Tel: +86‐551‐6516‐1139; Fax: +86‐551‐6516‐1139;

                E‐mail: xujiegou@ 123456ahmu.edu.cn

                and

                Hiroyuki Tsuda, Nanotoxicology Project, Nagoya City University, 3‐1 Tanabe‐Dohri, Mizuho‐ku, Nagoya 466‐8603, Japan.

                Tel: +81‐052‐836‐3496; Fax: +81‐052‐836‐3497;

                E‐mail: htsuda@ 123456phar.nagoya-cu.ac.jp

                Article
                CAS12954
                10.1111/cas.12954
                4946724
                27098557
                f52f3871-d88d-4540-a93f-4195314d4413
                © 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 14 March 2016
                : 17 April 2016
                : 19 April 2016
                Page count
                Pages: 12
                Funding
                Funded by: Princess Takamatsu Cancer Research Fund
                Award ID: H24
                Funded by: Health and Labor Sciences Research Grants of Japan
                Award ID: H21‐kagaku‐ippan‐008
                Award ID: H22‐kagaku‐ippan‐005
                Award ID: H24‐kagaku‐sitei‐009
                Award ID: H25‐kagaku‐ippan‐004
                Categories
                Original Article
                Original Articles
                Carcinogenesis
                Custom metadata
                2.0
                cas12954
                July 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.1 mode:remove_FC converted:15.07.2016

                Oncology & Radiotherapy
                intratracheal instillation,lung tumors,malignant mesothelioma,multiwalled carbon nanotubes,rat

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