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Published on: July 17, 2020
A novel oncoprotein Pirh2: rising from the shadow of MDM2
Zhihao Wang1, Bo Yang, Lanlan Dong
1School of Medicine, Wuhan University, Wuhan, China.
Abstract:
Pirh2 (p53-induced RING-H2) is an E3 ubiquitin ligase that can target p53 for degradation and thereby repress a diverse group of biological activities regulated by p53. Notably, Pirh2, rather than MDM2, is the primary degrader of active p53 under conditions of DNA damage. Moreover, Pirh2 is highly expressed in multiple cancer cell lines regardless of p53 status. Recent research has shown that Pirh2 is involved in many signalling pathways related to the genesis and evolution of cancer. This review aims to summarize a comprehensive picture of the role of Pirh2 in cellular processes and its significance to tumorigenesis. Furthermore, this review focuses on its potential role as a cancer therapeutic target.
Insights
Pirh2 (p53-induced RING-H2) is a key E3 ubiquitin ligase that degrades p53, impacting cancer cell pathways. Understanding Pirh2
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Pirh2 (p53-induced RING-H2) is an E3 ubiquitin ligase.
- Pirh2 targets p53 for degradation, inhibiting p53-regulated cellular activities.
- Pirh2 is the primary p53 degrader during DNA damage and is highly expressed in various cancer cell lines, irrespective of p53 status.
Purpose of the Study:
- To provide a comprehensive overview of Pirh2's function in cellular processes.
- To elucidate Pirh2's significance in cancer development and progression.
- To explore Pirh2 as a potential therapeutic target for cancer treatment.
Main Methods:
- Literature review of Pirh2's role in cellular signaling pathways.
- Analysis of Pirh2 expression patterns in cancer cell lines.
- Synthesis of current research on Pirh2's involvement in tumorigenesis.
Main Results:
- Pirh2 actively degrades p53, influencing diverse biological functions.
- Pirh2 plays a critical role in the genesis and evolution of cancer.
- Pirh2 is implicated in numerous cancer-related signaling pathways.
Conclusions:
- Pirh2 is a significant regulator of p53 stability and activity.
- Pirh2's dysregulation contributes to cancer development.
- Targeting Pirh2 presents a promising strategy for novel cancer therapies.
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