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Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats
Malignant mesothelioma (MM) is a rare but socially important neoplasm due to its association with asbestos exposure. Malignant mesothelioma is difficult to diagnose at an early stage, yet there are no particularly effective treatments available at the advanced stage, thus necessitating efficient str...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797813/ https://www.ncbi.nlm.nih.gov/pubmed/29193587 http://dx.doi.org/10.1111/cas.13460 |
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author | Ohara, Yuuki Chew, Shan‐Hwu Shibata, Takahiro Okazaki, Yasumasa Yamashita, Kyoko Toyokuni, Shinya |
author_facet | Ohara, Yuuki Chew, Shan‐Hwu Shibata, Takahiro Okazaki, Yasumasa Yamashita, Kyoko Toyokuni, Shinya |
author_sort | Ohara, Yuuki |
collection | PubMed |
description | Malignant mesothelioma (MM) is a rare but socially important neoplasm due to its association with asbestos exposure. Malignant mesothelioma is difficult to diagnose at an early stage, yet there are no particularly effective treatments available at the advanced stage, thus necessitating efficient strategies to prevent MM in individuals already exposed to asbestos. We previously showed that persistent oxidative damage caused by foreign body reaction and affinity of asbestos both to hemoglobin and histones is one of the major pathogeneses. Accordingly, as an effective strategy to prevent asbestos‐induced MM, we undertook the use of an iron chelator, deferasirox, which decreased the epithelial–mesenchymal transition in a crocidolite‐induced rat MM model. However, this agent may show adverse effects. Here, we studied the effects of iron removal by phlebotomy as a realistic measure on the same rat model. We injected a total of 5 mg crocidolite i.p. to F1 hybrid rats between the Fischer‐344 and Brown‐Norway strains at the age of 6 weeks. We repeated weekly or biweekly phlebotomy of 6‐8 mL/kg/time from 10 to 60 weeks of age. The animals were observed until 120 weeks. In male rats, phlebotomy significantly decreased the weight and nuclear grade of MM, and modestly reduced the associated ascites and the fraction of more malignant sarcomatoid subtype. Weekly phlebotomy prolonged long‐term survival. Our results indicate that appropriate phlebotomy may be a practical preventive measure to attenuate the initiation and promotion capacity of asbestos towards MM by reducing iron in individuals exposed to asbestos. |
format | Online Article Text |
id | pubmed-5797813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57978132018-02-14 Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats Ohara, Yuuki Chew, Shan‐Hwu Shibata, Takahiro Okazaki, Yasumasa Yamashita, Kyoko Toyokuni, Shinya Cancer Sci Original Articles Malignant mesothelioma (MM) is a rare but socially important neoplasm due to its association with asbestos exposure. Malignant mesothelioma is difficult to diagnose at an early stage, yet there are no particularly effective treatments available at the advanced stage, thus necessitating efficient strategies to prevent MM in individuals already exposed to asbestos. We previously showed that persistent oxidative damage caused by foreign body reaction and affinity of asbestos both to hemoglobin and histones is one of the major pathogeneses. Accordingly, as an effective strategy to prevent asbestos‐induced MM, we undertook the use of an iron chelator, deferasirox, which decreased the epithelial–mesenchymal transition in a crocidolite‐induced rat MM model. However, this agent may show adverse effects. Here, we studied the effects of iron removal by phlebotomy as a realistic measure on the same rat model. We injected a total of 5 mg crocidolite i.p. to F1 hybrid rats between the Fischer‐344 and Brown‐Norway strains at the age of 6 weeks. We repeated weekly or biweekly phlebotomy of 6‐8 mL/kg/time from 10 to 60 weeks of age. The animals were observed until 120 weeks. In male rats, phlebotomy significantly decreased the weight and nuclear grade of MM, and modestly reduced the associated ascites and the fraction of more malignant sarcomatoid subtype. Weekly phlebotomy prolonged long‐term survival. Our results indicate that appropriate phlebotomy may be a practical preventive measure to attenuate the initiation and promotion capacity of asbestos towards MM by reducing iron in individuals exposed to asbestos. John Wiley and Sons Inc. 2018-01-04 2018-02 /pmc/articles/PMC5797813/ /pubmed/29193587 http://dx.doi.org/10.1111/cas.13460 Text en © 2017 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 (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Ohara, Yuuki Chew, Shan‐Hwu Shibata, Takahiro Okazaki, Yasumasa Yamashita, Kyoko Toyokuni, Shinya Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
title | Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
title_full | Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
title_fullStr | Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
title_full_unstemmed | Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
title_short | Phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
title_sort | phlebotomy as a preventive measure for crocidolite‐induced mesothelioma in male rats |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797813/ https://www.ncbi.nlm.nih.gov/pubmed/29193587 http://dx.doi.org/10.1111/cas.13460 |
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