期刊
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 17, 期 12, 页码 -出版社
MDPI
DOI: 10.3390/ijms17122068
关键词
apoptosis; caspase-independent apoptosis (CIA); ferroptosis; necroptosis; autophagy; mitotic catastrophe; paraptosis; pyroptosis; efferocytosis
资金
- NIH [R01-CA174735-01A1]
Programmed cell death is a vital biological process for multicellular organisms to maintain cellular homeostasis, which is regulated in a complex manner. Over the past several years, apart from apoptosis, which is the principal mechanism of caspase-dependent cell death, research on non-apoptotic forms of programmed cell death has gained momentum. p53 is a well characterized tumor suppressor that controls cell proliferation and apoptosis and has also been linked to non-apoptotic, non-canonical cell death mechanisms. p53 impacts these non-canonical forms of cell death through transcriptional regulation of its downstream targets, as well as direct interactions with key players involved in these mechanisms, in a cell type-or tissue context-dependent manner. In this review article, we summarize and discuss the involvement of p53 in several non-canonical modes of cell death, including caspase-independent apoptosis (CIA), ferroptosis, necroptosis, autophagic cell death, mitotic catastrophe, paraptosis, and pyroptosis, as well as its role in efferocytosis which is the process of clearing dead or dying cells.
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