The good, the bad and the autophagosome: exploring unanswered questions of autophagy-dependent cell death

被引:97
|
作者
Kriel, Jurgen [1 ]
Loos, Ben [1 ]
机构
[1] Univ Stellenbosch, Dept Physiol Sci, ZA-7600 Stellenbosch, South Africa
来源
CELL DEATH AND DIFFERENTIATION | 2019年 / 26卷 / 04期
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
ADVANCED SOLID TUMORS; PHASE-I TRIAL; INDUCE AUTOPHAGY; CANCER-CELLS; STARVATION; APOPTOSIS; PHOSPHORYLATION; NECROSIS; AUTOSIS; HYDROXYCHLOROQUINE;
D O I
10.1038/s41418-018-0267-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The recent discovery of autosis as a variant of autophagy-dependent cell death has challenged the conventional understanding of cell death and programmed cell death in cellular decision making. In contrast to previous accounts of distinct cell death modalities, autosis occurs with high autophagic activity, in the absence of apoptotic and necrotic markers and yet is not fully regulated by typical autophagy markers. Given the metabolic importance of autophagic responses and the extensive cross-talk with both apoptosis and necrosis signalling, the classical and morphotype-driven characterization of cell death as pre-determined subroutines is being increasingly called into question. Furthermore, the conflicting evidence with regards to cell death induction through autophagy modulation in various cancer models highlights the lack of consensus over the extent to which autophagy assists in cell death ontrol and whether it is capable of being a bona fide lethal process. This review evaluates the evidence and context of autophagy-dependent cell death and delineates the role of an autophagic flux threshold associated with 'lethal' and 'non-lethal' autophagy and its role in autosis control. In doing so, cancer treatment avenues will be explored with regards to precision modulation of tumour autophagic flux to ascertain whether autosis induction may present a novel therapeutic strategy.
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页码:640 / 652
页数:13
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