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Several studies indicate that tumor cell metabolic reprogramming is governed by both inherent genetic alterations, such as the loss of tumor suppressors or the activation of oncogenes, and external influences from the tumor microenvironment, such as hypoxia, ROS, and other factors [49,50,51,52]

Similar and in some instances improved effects were also reported for AuNPs, which are emerging as promising agents for disease diagnosis [47,48,49] and therapy [3, 29, 50, 51]

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