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Published on: August 25, 2021
Parthanatos and its associated components: Promising therapeutic targets for cancer
Yunxiang Zhou1, Lihong Liu2, Sifeng Tao1
1Department of Surgical Oncology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, 310009, China.
Abstract:
Parthanatos is a PARP1-dependent, caspase-independent, cell-death pathway that is distinct from apoptosis, necrosis, or other known forms of cell death. Parthanatos is a multistep pathway that plays a pivotal role in tumorigenesis. There are many molecules in the parthanatos cascade that can be exploited to create therapeutic interventions for cancer management, including PARP1, PARG, ARH3, AIF, and MIF. These critical molecules are involved in tumor cell proliferation, progression, invasion, and metastasis. Therefore, these molecular signals in the parthanatos cascade represent promising therapeutic targets for cancer therapy. In addition, intimate interactions occur between parthanatos and other forms of cancer cell death, such as apoptosis and autophagy. Thus, co-targeting a combination of parthanatos and other death pathways may further provide a new avenue for cancer precision treatment. In this review, we elaborate on the signaling pathways of canonical parthanatos and briefly introduce the non-canonical parthanatos. We also shed light on the role parthanatos and its associated components play in tumorigenesis, particularly with respect to the aforementioned five molecules, and discuss the promise targeted therapy of parthanatos and its associated components holds for cancer therapy.
Insights
Parthanatos, a cell-death pathway, is crucial in cancer development. Targeting its key molecules offers promising cancer treatment strategies.
Area of Science:
- Oncology
- Cell Biology
- Molecular Biology
Background:
- Parthanatos is a distinct cell-death pathway, independent of caspases.
- This pathway plays a significant role in tumorigenesis and cancer progression.
Purpose of the Study:
- To review the signaling pathways of canonical and non-canonical parthanatos.
- To elucidate the role of parthanatos components in tumorigenesis.
- To discuss the therapeutic potential of targeting parthanatos in cancer therapy.
Main Methods:
- Review of existing literature on parthanatos signaling.
- Analysis of the role of key molecules (PARP1, PARG, ARH3, AIF, MIF) in cancer.
- Exploration of interactions between parthanatos and other cell-death pathways.
Main Results:
- Parthanatos involves multiple molecular steps critical for tumor cell proliferation, invasion, and metastasis.
- Key molecules like PARP1, PARG, ARH3, AIF, and MIF are implicated in cancer.
- Interactions with apoptosis and autophagy suggest combined therapeutic approaches.
Conclusions:
- Targeting parthanatos and its components presents a promising strategy for cancer therapy.
- Co-targeting parthanatos with other cell-death pathways may lead to novel precision cancer treatments.
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