Intra-tumor heterogeneity: lessons from microbial evolution and clinical implications

被引:0
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作者
Elza C de Bruin
Tiffany B Taylor
Charles Swanton
机构
[1] Translational Cancer Therapeutics Lab,
[2] UCL Cancer Institute,undefined
[3] University College London,undefined
[4] School of Biological Sciences,undefined
[5] University of Reading,undefined
[6] Translational Cancer Therapeutics Lab,undefined
[7] Cancer Research UK London Research Institute,undefined
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关键词
Epidermal Growth Factor Receptor; Acute Myeloid Leukemia; Resistant Clone; Beneficial Mutation; T790M Mutation;
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摘要
Multiple subclonal populations of tumor cells can coexist within the same tumor. This intra-tumor heterogeneity will have clinical implications and it is therefore important to identify factors that drive or suppress such heterogeneous tumor progression. Evolutionary biology can provide important insights into this process. In particular, experimental evolution studies of microbial populations, which exist as clonal populations that can diversify into multiple subclones, have revealed important evolutionary processes driving heterogeneity within a population. There are transferrable lessons that can be learnt from these studies that will help us to understand the process of intra-tumor heterogeneity in the clinical setting. In this review, we summarize drivers of microbial diversity that have been identified, such as mutation rate and environmental influences, and discuss how knowledge gained from microbial experimental evolution studies may guide us to identify and understand important selective factors that promote intra-tumor heterogeneity. Furthermore, we discuss how these factors could be used to direct and optimize research efforts to improve patient care, focusing on therapeutic resistance. Finally, we emphasize the need for longitudinal studies to address the impact of these potential tumor heterogeneity-promoting factors on drug resistance, metastatic potential and clinical outcome.
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