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Targeting cell death pathways for cancer therapy: recent developments in necroptosis, pyroptosis, ferroptosis, and
Xuhui Tong1,2, Rong Tang3,4, Mingming Xiao1,2
1Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No. 270 Dong'An Road, Shanghai, 200032, China.
Abstract:
Many types of human cells self-destruct to maintain biological homeostasis and defend the body against pathogenic substances. This process, called regulated cell death (RCD), is important for various biological activities, including the clearance of aberrant cells. Thus, RCD pathways represented by apoptosis have increased in importance as a target for the development of cancer medications in recent years. However, because tumor cells show avoidance to apoptosis, which causes treatment resistance and recurrence, numerous studies have been devoted to alternative cancer cell mortality processes, namely necroptosis, pyroptosis, ferroptosis, and cuproptosis; these RCD modalities have been extensively studied and shown to be crucial to cancer therapy effectiveness. Furthermore, evidence suggests that tumor cells undergoing regulated death may alter the immunogenicity of the tumor microenvironment (TME) to some extent, rendering it more suitable for inhibiting cancer progression and metastasis. In addition, other types of cells and components in the TME undergo the abovementioned forms of death and induce immune attacks on tumor cells, resulting in enhanced antitumor responses. Hence, this review discusses the molecular processes and features of necroptosis, pyroptosis, ferroptosis, and cuproptosis and the effects of these novel RCD modalities on tumor cell proliferation and cancer metastasis. Importantly, it introduces the complex effects of novel forms of tumor cell death on the TME and the regulated death of other cells in the TME that affect tumor biology. It also summarizes the potential agents and nanoparticles that induce or inhibit novel RCD pathways and their therapeutic effects on cancer based on evidence from in vivo and in vitro studies and reports clinical trials in which RCD inducers have been evaluated as treatments for cancer patients. Lastly, we also summarized the impact of modulating the RCD processes on cancer drug resistance and the advantages of adding RCD modulators to cancer treatment over conventional treatments.
Insights
Regulated cell death (RCD) pathways like apoptosis, necroptosis, pyroptosis, ferroptosis, and cuproptosis are crucial for cancer therapy. Modulating these RCD processes can overcome drug resistance and enhance antitumor immunity.
Area of Science:
- Cellular Biology
- Immunology
- Oncology
Background:
- Regulated cell death (RCD) is vital for homeostasis and defense, with apoptosis being a key pathway.
- Tumor cells often evade apoptosis, leading to treatment resistance and recurrence.
- Alternative RCD pathways—necroptosis, pyroptosis, ferroptosis, and cuproptosis—are critical for cancer therapy effectiveness.
Purpose of the Study:
- To review the molecular mechanisms of necroptosis, pyroptosis, ferroptosis, and cuproptosis.
- To explore the impact of these RCD modalities on tumor cell proliferation, metastasis, and the tumor microenvironment (TME).
- To summarize therapeutic agents and nanoparticles targeting RCD pathways in cancer treatment.
Main Methods:
- Literature review of molecular processes and features of RCD pathways.
- Analysis of studies on the effects of RCD on tumor biology and the TME.
- Compilation of data from in vitro, in vivo, and clinical trials of RCD modulators.
Main Results:
- Novel RCD pathways significantly influence tumor cell proliferation and metastasis.
- Tumor cell death can alter TME immunogenicity, enhancing antitumor responses.
- RCD modulators show therapeutic potential, impacting cancer drug resistance.
Conclusions:
- Necroptosis, pyroptosis, ferroptosis, and cuproptosis are promising therapeutic targets in oncology.
- Modulating RCD can overcome cancer drug resistance and improve treatment outcomes.
- Targeting RCD pathways offers advantages over conventional cancer treatments.
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