The energy buffering ability of creane appears to able to protect cells from excessive DNA damage induced by free radicals, which seem to, in part, work through ATP depleon. This appears to be more protecve of mitochondrial DNA than it is of nuclear DNA. In rats experiencing toxic levels of doxorubicin (a chemotherapeuc agent), creane supplementaon at 0.2g/kg for 30 days appeared to significantly protect rats from death and reduced serum levels of LDH and ALT. The two enzymes were further reduced with the addion of 0.25mg/kg Vitamin C and 400IU/kg Vitamin E . In children with lymphoblastic leukemia, who are maintaining corticosteroid chemotherapy, creatine monohydrate at 0.1g/kg is able to significantly attenuate the chemotherapy-induced gain in fat mass over 16 weeks. [450] In a sample of people with colorectal cancer, to whom creatine supplementation was given for 8 weeks to assess its interactions with chemotherapy, creatine failed to benefit muscle function or quality of life. Benefit was seen in body cell mass and phase angle (indicative of cellular viability), but only in the subsample with less aggressive chemotherapy. References : Santos RV, et al. Chronic supplementaon of creane and vitamins C and E increases survival and improves biochemical parameters aſter Doxorubicin treatment in rats . Clin Exp Pharmacol Physiol . (2007) Bourgeois JM, et al. Creane monohydrate aenuates body fat accumulaon in children with acute lymphoblasc leukemia during maintenance chemotherapy . Pediatr Blood Cancer. (2008) Kim HJ, et al. Studies on the safety of creane supplementaon . Amino Acids. (2011) *Norman K, et al. Effects of creane supplementaon on nutrional status, muscle funcon and quality of life in paents with colorectal cancer--a double blind randomised controlled trial . Clin Nutr. (2006)