Triggering Pyroptosis in Cancer

被引:3
作者
Johnson, Daniel E. [1 ,2 ]
Cui, Zhibin [3 ]
机构
[1] Univ Calif San Francisco, Dept Otolaryngol Head & Neck Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[3] SUNY Buffalo, Sch Dent Med, Dept Oral Biol, Buffalo, NY 14214 USA
关键词
cancer; pyroptosis; cell death; chemotherapy drugs; caspase-1; gasdermin; IL-1b; IL-18; GSDM-E; natural products; LPS; DIPEPTIDYL PEPTIDASE-IV; NF-KAPPA-B; INDUCE PYROPTOSIS; GASDERMIN D; CELL; ACTIVATION; CURCUMIN; INHIBITORS; CISPLATIN; APOPTOSIS;
D O I
10.3390/biom15030348
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
Pyroptosis is an inflammatory programmed cell death recently identified as a crucial cellular process in various diseases, including cancers. Unlike other forms of cell death, canonical pyroptosis involves the specific cleavage of gasdermin by caspase-1, resulting in cell membrane damage and the release of the pro-inflammatory cytokines IL-1 beta and IL-18. Initially observed in innate immune cells responding to external pathogens or internal death signals, pyroptotic cell death has now been observed in numerous cell types. Recent studies have extensively explored different ways to trigger pyroptotic cell death in solid tumors, presenting a promising avenue for cancer treatment. This review outlines the mechanisms of both canonical and noncanonical pyroptosis pertinent to cancer and primarily focuses on various biomolecules that can induce pyroptosis in malignancies. This strategy aims not only to eliminate cancer cells but also to promote an improved tumor immune microenvironment. Furthermore, emerging research indicates that targeting pyroptotic pathways may improve the effectiveness of existing cancer treatments, making them more potent against resistant tumor types, offering new hope for overcoming treatment resistance in aggressive malignancies.
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页数:16
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