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Updated: Mar 21, 2026

An In Vitro System to Study Tumor Dormancy and the Switch to Metastatic Growth
Published on: August 11, 2011
Ageing influences tumour-niche interactions: Implications for metastatic dormancy, reawakening and recurrence
Gillian M Mackie1, Frances K Turrell1
1Tumour Microenvironment and Metastasis Group, Manchester Breast Centre and Manchester Cancer Research Centre, Division of Cancer Sciences, Oglesby Cancer Research Building, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, M20 4GJ, UK.
Abstract:
Many cancer patients remain at risk of metastatic relapse for the remainder of their lives, despite initial disease remission, due to disseminated tumour cells (DTCs) persisting at secondary sites in a dormant, therapy-resistant state. Dormant DTCs can reawaken and develop into clinical metastasis after a prolonged latency period. Interactions between DTCs and their niche are key to metastatic dormancy and subsequent reawakening and outgrowth. Ageing has profound effects on tissues and the immune system and, as such, the field is evolving to delineate the impact of an aged microenvironment on metastatic dormancy. We summarise the latest insights in this review, focussing on recent advances in immune- and stroma-mediated regulation of dormancy and reawakening in the context of age-related microenvironmental perturbations.
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