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探讨细胞皱缩现象作为癌症治疗的一种治疗方法。

Exploring paraptosis as a therapeutic approach in cancer treatment.

机构信息

Center for Molecular Medicine, China Medical University Hospital, Taichung, 406040, Taiwan.

Research Center for Cancer Biology, China Medical University, Taichung, 406040, Taiwan.

出版信息

J Biomed Sci. 2024 Nov 4;31(1):101. doi: 10.1186/s12929-024-01089-4.

DOI:10.1186/s12929-024-01089-4
PMID:39497143
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11533606/
Abstract

A variety of cell death pathways play critical roles in the onset and progression of multiple diseases. Paraptosis, a unique form of programmed cell death, has gained significant attention in recent years. Unlike apoptosis and necrosis, paraptosis is characterized by cytoplasmic vacuolization, swelling of the endoplasmic reticulum and mitochondria, and the absence of caspase activation. Numerous natural products, synthetic compounds, and newly launched nanomedicines have been demonstrated to prime cell death through the paraptotic program and may offer novel therapeutic strategies for cancer treatment. This review summarizes recent findings, delineates the intricate network of signaling pathways underlying paraptosis, and discusses the potential therapeutic implications of targeting paraptosis in cancer treatment. The aim of this review is to expand our understanding of this unique cell death process and explore the potential therapeutic implications of targeting paraptosis in cancer treatment.

摘要

多种细胞死亡途径在多种疾病的发生和进展中起着关键作用。细胞程序性坏死的一种独特形式,已引起近年来的广泛关注。与细胞凋亡和细胞坏死不同,细胞程序性坏死的特征是细胞质空泡化、内质网和线粒体肿胀,以及缺乏半胱天冬酶激活。许多天然产物、合成化合物和新推出的纳米药物已被证明可通过细胞程序性坏死途径引发细胞死亡,并可能为癌症治疗提供新的治疗策略。本综述总结了最近的发现,阐述了细胞程序性坏死的信号通路的复杂网络,并讨论了针对癌症治疗中细胞程序性坏死的潜在治疗意义。本综述的目的是扩展我们对这种独特的细胞死亡过程的理解,并探索针对癌症治疗中细胞程序性坏死的潜在治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/5beb26407527/12929_2024_1089_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/cdeef6bae12a/12929_2024_1089_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/574096311eb0/12929_2024_1089_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/db50f44fc24f/12929_2024_1089_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/5beb26407527/12929_2024_1089_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/cdeef6bae12a/12929_2024_1089_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/574096311eb0/12929_2024_1089_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/db50f44fc24f/12929_2024_1089_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a396/11533606/5beb26407527/12929_2024_1089_Fig4_HTML.jpg

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本文引用的文献

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Cell Biosci. 2024 Jun 10;14(1):78. doi: 10.1186/s13578-024-01260-2.
2
Kaempferide triggers apoptosis and paraptosis in pancreatic tumor cells by modulating the ROS production, SHP-1 expression, and the STAT3 pathway.山奈酚通过调节 ROS 产生、SHP-1 表达和 STAT3 通路诱导胰腺肿瘤细胞凋亡和副凋亡。
IUBMB Life. 2024 Sep;76(9):745-759. doi: 10.1002/iub.2827. Epub 2024 May 6.
3
α-Hederin induces paraptosis by targeting GPCRs to activate Ca/MAPK signaling pathway in colorectal cancer.
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Vet Comp Oncol. 2025 Sep;23(3):377-387. doi: 10.1111/vco.13062. Epub 2025 Apr 15.
α-常春藤皂苷通过靶向G蛋白偶联受体激活钙/丝裂原活化蛋白激酶信号通路,从而在结直肠癌中诱导副凋亡。
Cancer Med. 2024 Apr;13(8):e7202. doi: 10.1002/cam4.7202.
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Apoptosis and Paraptosis Induced by Disulfiram-Loaded Ca/Cu Dual-Ions Nano Trap for Breast Cancer Treatment.载双硫仑的 Ca/Cu 双离子纳米陷阱诱导的乳腺癌治疗中的细胞凋亡和副凋亡。
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