Abstract
Reactive oxygen species (ROS) results from various metabolic processes and plays a significant role as secondary messengers across multiple signaling pathways. However, any disruption in the delicate balance of optimum ROS levels and regulatory antioxidant molecules can lead to enhanced oxidative stress, proving detrimental to the cell homeostatic functioning. The major repercussion observed in the mammalian system is the pro-tumorigenic impact of the upregulated ROS levels in tumor initiation, progression, and metastasis. Hence, robust diagnostic and prognostic tools need to be developed to screen and target ROS in cancer patients. This chapter highlights the different clinical therapies currently employed to detect and suppress the elevated ROS levels within the tumor cells. These therapies include drug-based therapies, immunotherapies, radiation-based therapies like photodynamic therapy (PDT) and sonodynamic therapy (SDT), inhibitors such as HSP90 and Mn porphyrins, and other targeted remedies like vaccines, monoclonal antibodies, and hydrogen gas application. Summarizing such commonly used clinical practices at a single platform facilitates a comparative analysis for their efficiency and adaptability.
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Sengar, A., Sengar, M., Mann, Z., Raghav, P.K. (2022). Clinical Approaches in Targeting ROS-Induced Cancer. In: Chakraborti, S. (eds) Handbook of Oxidative Stress in Cancer: Therapeutic Aspects. Springer, Singapore. https://doi.org/10.1007/978-981-16-5422-0_256
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DOI: https://doi.org/10.1007/978-981-16-5422-0_256
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