坏死性下垂
自噬
程序性细胞死亡
背景(考古学)
癌症研究
癌症
癌细胞
溶瘤病毒
时尚
细胞生物学
半胱氨酸蛋白酶
细胞凋亡
生物
肿瘤细胞
生物化学
古生物学
遗传学
作者
Monika Yadav,Karishma Niveria,Tapas Sen,Indrajit Roy,Anita Verma
出处
期刊:Nanomedicine
日期:2021-05-01
卷期号:16 (12): 1049-1065
被引量:10
标识
DOI:10.2217/nnm-2020-0443
摘要
Apoptotic death evasion is a hallmark of cancer progression. In this context, past decades have witnessed cytotoxic agents targeting apoptosis. However, owing to cellular defects in the apoptotic machinery, tumors develop resistance to apoptosis-based cancer therapies. Hence, targeting nonapoptotic cell-death pathways displays enhanced therapeutic success in apoptosis-defective tumor cells. Exploitation of multifunctional properties of engineered nanoparticles may allow cancer therapeutics to target yet unexplored pathways such as ferroptosis, autophagy and necroptosis. Necroptosis presents a programmed necrotic death initiated by same apoptotic death signals that are caspase independent, whereas autophagy is self-degradative causing vacuolation, and ferroptosis is an iron-dependent form driven by lipid peroxidation. Targeting these tightly regulated nonapoptotic pathways may emerge as a new direction in cancer drug development, diagnostics and novel cancer nanotherapeutics. This review highlights the current challenges along with the advancement in this field of research and finally summarizes the future perspective in terms of their clinical merits.
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