4.7 Article

The dose makes the poison

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 621, Issue -, Pages 649-653

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.scitotenv.2017.11.218

Keywords

Microcystin; Low-dose; Tumor; Equivalent doses; Inter-species variations; Experimental design

Funding

  1. National Natural Science Foundations of China [31770555, 31600423]
  2. State Key Laboratory of Freshwater Ecology and Biotechnology [2016FBZ08]
  3. High Level Foreign Experts program - State Administration of Foreign Experts Affairs, the P.R. China [GDT20143200016]
  4. Einstein Professor Program of the Chinese Academy of Sciences
  5. Canada Research Chair program
  6. Distinguished Visiting Professorship in the School of Biological Sciences of the University of Hong Kong

Ask authors/readers for more resources

Some microcystins (MCs) might cause hepatotoxicity in animals and humans. MC-LR is also a tumor promoter and a suspect carcinogen. In 2010, the International Agency for Research on Cancer (IARC) classified MC-LR as a possible human carcinogen (Group 2B). Recently, an article entitled Long-term, low-dose exposure to microcystin toxin does not increase the risk of liver tumor development or growth in micewas published in Hepatology Research by Meaghan Labine and Gerald Y. Minuk. However, the experimental design was flawed and the conclusion is misleading. 1 mu g/L MC-LR in drinking water is the provisional guideline value established by the World Health Organization (WHO) for humans in 1998, based on a tolerable daily intake (TDI) of 0.04 mu g/kg body mass (BM). Assuming the mice drink 1.5 mL/10 g BM of water per day, the exposure dose would be 0.15 mu g/kg/d BM, about 270-fold less than 40 mu g/kg/d, the no-observed-adverse-effect level (NOAEL). Thus, the dose of MC-LR was too small and unlikely to result in liver tumor development or enhance existing tumor growth, even with a long-term (28 weeks) exposure. Presumably, they didn't consider inter-species variations between mice and humans, including toxicokinetics and toxicodynamics. Ranges of low-doseMCs for animals and humans should be defined. Also, the authorsmisunderstood or misrepresented several previous studies. Before drawing final conclusions on the carcinogenicity of MCs, further well-designed experiments are warranted. (C) 2017 Elsevier B.V. All rights reserved.

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