Researchers discover how leukaemia-associated gene mutations steadily commandeer blood cell production over a lifetime, and how these changes relate to ageing and cancer development. The new study is published in Nature.
New research by scientists at the German Cancer Research Center (DKFZ), the Wellcome Sanger Institute, the Cambridge Stem Cell Institute, EMBL's European Bioinformatics Institute (EMBL-EBI) and collaborators has uncovered how genetic mutations hijack the production of blood cells in different periods of life, and how these changes relate to ageing and the development of age-related diseases, including blood cancer. The new study represents the first time that the lifelong impact of genetic mutations on cell growth dynamics has been explored.
All human cells acquire genetic changes in their DNA throughout life, known as somatic mutations, with a specific subset of mutations driving cells to multiply. This is common in professional blood making cells, known as blood stem cells, and results in the growth of populations of cells with identical mutations known as 'clones'. This process, termed 'clonal haematopoiesis', becomes ubiquitous with age, and is a risk factor for developing blood cancer, and other age-related conditions.
To understand how and when clonal haematopoiesis develops, how it is influenced by ageing, and how it relates to disease, the researchers tracked nearly 700 blood cell clones from 385 individuals aged over 55, who were part of the SardiNIA longitudinal study . Participants donated regular blood samples for up to 16 years.
DNA sequencing of blood samples showed that 92.4 per cent of clones expanded at a stable exponential rate over the period studied. The rate of growth was primarily influenced by the nature of the mutated gene in each clone. After capturing the behaviour of clones in later life, the team used mathematical models to infer their growth patterns over the entire human lifespan. They uncovered that clone behaviour changed dramatically with age depending on the identity of the mutated gene. First, clones driven by mutations in DNMT3A, expanded fast in young people and then decelerated in old age. Second, clones driven by mutations in TET2 appeared and grew uniformly throughout life, such that they became more common than DNMT3A-mutant clones after the age of 75. Finally, clones with mutations in splicing genes, U2AF1 and SRSF2, only expanded exclusively later in life and exhibited some of the fastest growth. These age-dependent clonal behaviours mirror the frequency of emergence of different types of blood cancers and reveal that mutations associated with fast clonal growth are more likely to lead to malignancy.
Moritz Gerstung, co-senior author of the study, from EMBL's European Bioinformatics Institute and the German Cancer Research Centre (DKFZ), said: "For the first time we have been able to use genomic analysis to understand the past, present and future of mutant clones in our blood. These data show that the dynamics of blood clones are surprisingly predictable over a period of years, but also highlight that they change over a lifetime in ways we don't understand yet."
Margarete Fabre, lead researcher on the study and PhD student at the Wellcome Sanger Institute and the University of Cambridge, said: "Our findings reveal how acquired genetic DNA changes hijack blood formation during our lifetimes, with normal blood stem cells competing against cells with pre-leukaemia mutations. Understanding why some mutations prevail in youth and others in old age could help us find ways to maintain the health and diversity of our blood cells."
George Vassiliou, co-senior author of the study, formerly from the Wellcome Sanger Institute, and now at the Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, and Cambridge University Hospitals, said: "Collectively, our work reveals an astonishing interaction between advancing age and mutations in the DNA of our blood cells that is played out as the expansion of cells with different mutations at different ages.
Remarkably, these changes lead to the emergence of different types of blood cancers at different ages, and with different risks of progression. With this new understanding, researchers can begin to develop approaches and treatments to stop the development of blood cancer in its tracks."
Research Publication: Margarete A. Fabre, José Guilherme de Almeida, Edoardo Fiorillo, Emily Mitchell, Aristi Damaskou, Justyna Rak, Valeria Orrù, Michele Marongiu, MS Vijayabaskar, Joanna Baxter, Claire Hardy, Federico Abascal, Michael Spencer Chapman, Nicholas Williams, Jyoti Nangalia, Iñigo Martincorena, Peter J. Campbell, Eoin F. McKinney, Francesco Cucca, Moritz Gerstung, George S. Vassiliou: The longitudinal dynamics and natural history of clonal haematopoiesis. Nature 2022, DOI: 10.1038/s41586-022-04785-z