4.7 Article

5-Fluorouracil causes severe CNS demyelination by disruption of TCF7L2/HDAC1/HDAC2 complex in adolescent mice

Journal

TOXICOLOGY
Volume 325, Issue -, Pages 144-150

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.tox.2014.08.011

Keywords

5-FU; TCF7L2; Demyelination; Adolescence; Oligodendrocyte

Funding

  1. National Natural Science Foundation [81202606, 81170607, 81000263]
  2. Zhejiang Provincial Natural Science Foundation [LY12C12001]
  3. Fundamental Research Funds for the Central Universities
  4. National Key Technology Research and Development Program of the Ministry of Science and Technology of China [2013BAD19B05]

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Several studies have showed the anti-cancer efficacy of 5-FU (5-fluorouracil) on pediatric tumors. Although the delayed demyelination induced by 5-FU in adult patients has been reported, the effect of 5-FU on oligodendrocyte myelination in adolescence is still unknown. Here, we demonstrate that systemic administration with 5-FU leads to immediate demyelination in the central nervous system (CNS) of adolescent mice, which is mainly attributed to the death of OLs. Gene-chip microarray transcriptome analysis identifies that oligodendrocyte-specific factor TCF7L2 may be a toxic target of 5-FU-impaired myelination. 5-FU-decreased TCF7L2 results in disruption of the interaction between TCF7L2 and HDAC1/2. Inhibition of crucial myelination-promoting factors by 5-FU is more significantly antagonized by cotransfection of TCF7L2, HDAC1 and HDAC2 than TCF7L2 alone. Our findings reveal that 5-FU could acutely induce the severe myelin degeneration in adolescence and disruption of TCF7L2/HDAC1/HDAC2 complex is at least partially involved in 5-FU-induced demyelination. (C) 2014 Elsevier Ireland Ltd. All rights reserved.

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