Radiation therapy-related toxicity is becoming increasingly important as cancer treatment outcomes improve. It is common for radiation to damage cancer cells and normal cells by hydrolyzing H2O which leading to free radicals production. Response transcription factors and signal transduction pathways are activated, resulting in DNA damage. Natural antioxidants have attracted a lot of attention. My study aimed to assess the effectiveness of cactus cladode extract (CCE) in protecting DNA plasmids against γ-radiation. The samples were irradiated with 137Cs γ-rays at different doses in the absence or presence of CCE. Agarose gel electrophoresis analysis shows that the aqueous CCE prevents radiation-induced DNA damage. Indeed, the yields of SSB and DSBs are (78 ± 3) x10−4/Gy/plasmid and (0.75 ± 0.09) x 10−4/Gy/plasmid, respectively. However, the greatest fits for the yields for SSB and DSB forming, in the presence of CCE1 (0.5 μg), are (44 ± 2) x10−4/Gy/plasmid and (0.55 ± 0.05) x 10−4/Gy/plasmid, respectively. Despite, the yields for SSB and DSB formation in the presence of CCE2 (1 μg), are (31 ± 2) x10−4/Gy/plasmid and (0.48 ± 0.09) x 10−4/Gy/plasmid, respectively. While, the yields for SSB and DSB formation, in the presence of CCE3 (1.5 μg), are (22 ± 2) x10−4/Gy/plasmid and (0.4 ± 0.02) x 10−4/Gy/plasmid, respectively. Moreover, the CCE efficiently inhibit DNA base damage. A decrease of 70%, 83%, and 87% of the Nth-sensitive sites was found when the sample was irradiated with CCE1, CCE2, and CCE3, respectively. Moreover, we calculated a decrease of 66%, 79%, and 82% of the Fpg-sensitive sites when the sample was irradiated with CCE1, CCE2, and CCE3, respectively. In conclusion, my results indicate that the CCE is a potent radioprotector and hydroxyl radical scavenger; it efficiently inhibits DNA SSBs, DSBs and base damage. It suggests that this extract may be able to protect against genotoxicity, apoptosis, and nephrotoxicity.
Read full abstract