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DNA damage signalling from the placenta to foetal blood as a potential mechanism for childhood leukaemia initiation

Research output: Contribution to journalArticle

Original languageEnglish
Article number4370
Number of pages17
JournalScientific Reports
Volume9
Issue number1
DOIs
DateAccepted/In press - 6 Nov 2018
DatePublished (current) - 13 Mar 2019

Abstract

For many diseases with a foetal origin, the cause for the disease initiation remains unknown. Common childhood acute leukaemia is thought to be caused by two hits, the first in utero and the second in childhood in response to infection. The mechanism for the initial DNA damaging event are unknown. Here we have used in vitro, ex vivo and in vivo models to show that a placental barrier will respond to agents that are suspected of initiating childhood leukaemia by releasing factors that cause DNA damage in cord blood and bone marrow cells,
including stem cells. We show that DNA damage caused by in utero exposure can reappear postnatally after an immune challenge. Furthermore, both foetal and postnatal DNA damage are prevented by prenatal exposure of the placenta to a mitochondrially-targeted antioxidant.
We conclude that the placenta might contribute to the first hit towards leukaemia initiation by bystander-like signalling to foetal haematopoietic cells.

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via Springer Nature at https://www.nature.com/articles/s41598-019-39552-0. Please refer to any applicable terms of use of the publisher.

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