自噬
阿霉素
癌症
抗药性
癌症研究
药理学
蒽环类
拓扑异构酶
癌症治疗
医学
生物
体外
化疗
细胞凋亡
乳腺癌
内科学
生物化学
微生物学
作者
Chao Chen,Lu Lu,Shichao Yan,Huimei Yi,Hui Yao,Di Wu,Guangchun He,Xiaojun Tao,Xiyun Deng
出处
期刊:Anti-Cancer Drugs
[Ovid Technologies (Wolters Kluwer)]
日期:2018-01-01
卷期号:29 (1): 1-9
被引量:144
标识
DOI:10.1097/cad.0000000000000572
摘要
Doxorubicin (DOX), also known as adriamycin, is a DNA topoisomerase II inhibitor and belongs to the family of anthracycline anticancer drugs. DOX is used for the treatment of a wide variety of cancer types. However, resistance among cancer cells has emerged as a major barrier to effective treatment using DOX. Currently, the role of autophagy in cancer resistance to DOX and the mechanisms involved have become one of the areas of intense investigation. More and more preclinical data are being obtained on reversing DOX resistance through modulation of autophagy as one of the promising therapeutic strategies. This review summarizes the recent advances in autophagy-targeting therapies that overcome DOX resistance from in-vitro studies to animal models for exploration of novel delivery systems. In-depth understanding of the mechanisms of autophagy regulation in relation to DOX resistance and development of molecularly targeted autophagy-modulating agents will provide a promising therapeutic strategy for overcoming DOX resistance in cancer treatment.
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