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Programmed cell death pathways in cancer: a review of apoptosis, autophagy and programmed necrosis
1State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Abstract:
Programmed cell death (PCD), referring to apoptosis, autophagy and programmed necrosis, is proposed to be death of a cell in any pathological format, when mediated by an intracellular program. These three forms of PCD may jointly decide the fate of cells of malignant neoplasms; apoptosis and programmed necrosis invariably contribute to cell death, whereas autophagy can play either pro-survival or pro-death roles. Recent bulk of accumulating evidence has contributed to a wealth of knowledge facilitating better understanding of cancer initiation and progression with the three distinctive types of cell death. To be able to decipher PCD signalling pathways may aid development of new targeted anti-cancer therapeutic strategies. Thus in this review, we present a brief outline of apoptosis, autophagy and programmed necrosis pathways and apoptosis-related microRNA regulation, in cancer. Taken together, understanding PCD and the complex interplay between apoptosis, autophagy and programmed necrosis may ultimately allow scientists and clinicians to harness the three types of PCD for discovery of further novel drug targets, in the future cancer treatment.
Insights
Programmed cell death (PCD), including apoptosis, autophagy, and programmed necrosis, plays a crucial role in cancer. Understanding these pathways could lead to new cancer treatments targeting cell death mechanisms.
Area of Science:
- Oncology
- Cell Biology
Background:
- Programmed cell death (PCD) encompasses apoptosis, autophagy, and programmed necrosis, all intracellularly regulated cell death processes.
- These PCD pathways are integral to the fate of malignant neoplasms, with apoptosis and programmed necrosis promoting cell death, while autophagy can be pro-survival or pro-death.
- Accumulating evidence enhances our understanding of cancer initiation and progression through these distinct cell death types.
Purpose of the Study:
- To review the signaling pathways of apoptosis, autophagy, and programmed necrosis in cancer.
- To discuss the regulation of apoptosis by microRNAs in the context of cancer.
- To highlight the potential of deciphering PCD pathways for developing targeted anti-cancer therapeutics.
Main Methods:
- Literature review of programmed cell death pathways.
- Analysis of the interplay between apoptosis, autophagy, and programmed necrosis in cancer.
- Examination of microRNA regulation in apoptosis related to cancer.
Main Results:
- Apoptosis and programmed necrosis are consistently cell-lethal, whereas autophagy exhibits dual roles in cancer cell survival and death.
- Detailed understanding of PCD pathways is crucial for cancer research.
- MicroRNA regulation of apoptosis is a significant factor in cancer progression.
Conclusions:
- Deciphering PCD signaling pathways offers a promising avenue for novel targeted anti-cancer therapeutic strategies.
- Harnessing the complex interplay of apoptosis, autophagy, and programmed necrosis can lead to the discovery of new drug targets for future cancer treatment.
- Further research into PCD mechanisms is essential for advancing cancer therapy.
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