阿霉素
免疫原性细胞死亡
心脏毒性
药品
药理学
拓扑异构酶
癌症研究
癌细胞
化学
癌症
化疗
生物
医学
体外
生物化学
内科学
作者
Sruthi Sritharan,N Sivalingam
出处
期刊:Life Sciences
[Elsevier]
日期:2021-04-20
卷期号:278: 119527-119527
被引量:228
标识
DOI:10.1016/j.lfs.2021.119527
摘要
Doxorubicin or Adriamycin, is one of the most widely used chemotherapeutic drug for treating a myriad of cancers. It induces cell death through multiple intracellular targets: reactive oxygen species generation, DNA-adduct formation, topoisomerase II inhibition, histone eviction, Ca2+ and iron hemostasis regulation, and ceramide overproduction. Moreover, doxorubicin-treated dying cells undergo cellular modifications that enable neighboring dendritic cell activation and enhanced presentation of tumor antigen. In addition, doxorubicin also aids in the immune-mediated clearance of tumor cells. However, the development of chemoresistance and cardiotoxicity side effect has undermined its widespread applicability. Several formulations of doxorubicin and co-treatments with inhibitors, miRNAs, natural compounds and other chemotherapeutic drugs have been essential in reducing its dosage-dependent toxicity and combating the development of resistance. Further, more advanced research into the molecular mechanism of chemoresistance development would be vital in improving the overall survivability of clinical patients and in preventing cancer relapse.
科研通智能强力驱动
Strongly Powered by AbleSci AI