Author:
Mitchell Emily,Pham My H.,Clay Anna,Sanghvi Rashesh,Pietsch Sandra,Hsu Joanne I.,Jung Hyunchul,Vedi Aditi,Moody Sarah,Wang Jingwei,Leonganmornlert Daniel,Chapman Michael Spencer,Williams Nicholas,Dunstone Ellie,Santarsieri Anna,Cagan Alex,Machado Heather E.,Baxter Joanna,Follows George,Hodson Daniel J,McDermott Ultan,Doherty Gary J.,Martincorena Inigo,Humphreys Laura,Mahbubani Krishnaa,Parsy Kourosh Saeb,Takahashi Koichi,Goodell Margaret A.,Kent David,Laurenti Elisa,Campbell Peter J.,Rahbari Raheleh,Nangalia Jyoti,Stratton Michael R.
Abstract
AbstractIn developed countries, ∼10% of individuals are exposed to systemic chemotherapy for cancer and other diseases. Many chemotherapeutic agents act by increasing DNA damage in cancer cells, triggering cell death. However, there is limited understanding of the extent and long-term consequences of collateral DNA damage to normal tissues. To investigate the impact of chemotherapy on mutation burdens and cell population structure of a normal tissue we sequenced blood cell genomes from 23 individuals, aged 3–80 years, treated with a range of chemotherapy regimens. Substantial additional mutation loads with characteristic mutational signatures were imposed by some chemotherapeutic agents, but there were differences in burden between different classes of agent, different agents of the same class and different blood cell types. Chemotherapy also induced premature changes in the cell population structure of normal blood, similar to those of normal ageing. The results constitute an initial survey of the long-term biological consequences of cytotoxic agents to which a substantial fraction of the population is exposed during the course of their disease management, raising mechanistic questions and highlighting opportunities for mitigation of adverse effects.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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