Newly synthesized phenanthroimidazole derivatives L082 as a safe anti-tumor and anti-injury inflammation bifunctional compound

炎症 氧化应激 药理学 化疗 医学 体内 消炎药 癌症 免疫学 外科 内科学 生物 生物技术
作者
Shi-Feng Lai,Ruotong Liu,Wen-Hui Peng,Xiaoting Huang,Xicheng Wang,Jiayi Qian,Wenjie Mei,Miao Cheng,Teng Wang,Baoguo Wang
出处
期刊:European Journal of Pharmacology [Elsevier]
卷期号:889: 173571-173571 被引量:2
标识
DOI:10.1016/j.ejphar.2020.173571
摘要

Chemotherapy drugs exerts beneficial antitumor activity before and after cancer surgery. Post-injury complications are a potential hazard after surgical tumor resection. Inflammation caused by surgical stress is known to promote the progression of post-injury complications. Recent studies have found that chemotherapy drugs can promote post-injury inflammatory response, leading to increased post-injury complications. Imidazole derivatives have effective anticancer activity. However, the impact of post-operative inflammation caused by imidazole derivatives is unclear. In this study, two novel phenanthroimidazole derivatives (L082 and L142) were synthesized and characterized. These compounds showed significant inhibitory effects on different tumor cells. The compound L082 also inhibited liver cancer in vivo. In addition, L082 played a significant role in inhibiting the accumulation of inflammatory cells and promoting the elimination of inflammatory cells at the incision, which may be related to inhibiting the production of ROS and NO in oxidative and nitric stress. These results suggest that L082 can be used as a bifunctional drug to suppress tumors and reduce post-injury inflammation complications.
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