MISC

査読有り
2018年2月1日

Phlebotomy as a preventive measure for crocidolite-induced mesothelioma in male rats

Cancer Science
  • Yuuki Ohara
  • ,
  • Shan-Hwu Chew
  • ,
  • Takahiro Shibata
  • ,
  • Yasumasa Okazaki
  • ,
  • Kyoko Yamashita
  • ,
  • Shinya Toyokuni

109
2
開始ページ
330
終了ページ
339
記述言語
英語
掲載種別
速報,短報,研究ノート等(学術雑誌)
DOI
10.1111/cas.13460
出版者・発行元
Blackwell Publishing Ltd

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.

リンク情報
DOI
https://doi.org/10.1111/cas.13460
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/29193587
ID情報
  • DOI : 10.1111/cas.13460
  • ISSN : 1349-7006
  • ISSN : 1347-9032
  • PubMed ID : 29193587
  • SCOPUS ID : 85041454054

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