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Purification of Ubiquitinated p53 Proteins from Mammalian Cells
Published on: March 21, 2022
Deubiquitylase OTUD3 regulates PTEN stability and suppresses tumorigenesis
Lin Yuan1,2, Yanrong Lv3, Hongchang Li1
1State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Collaborative Innovation Center for Cancer Medicine, Beijing 100850, China.
Abstract:
PTEN is one of the most frequently mutated tumour suppressors and reduction in PTEN protein stability also plays a role in tumorigenesis. Although several ubiquitin ligases for PTEN have been identified, the deubiquitylase for de-polyubiquitylation and stabilization of PTEN is less defined. Here, we report OTUD3 as a deubiquitylase of PTEN. OTUD3 interacts with, de-polyubiquitylates and stabilizes PTEN. Depletion of OTUD3 leads to the activation of Akt signalling, induction of cellular transformation and cancer metastasis. OTUD3 transgenic mice exhibit higher levels of the PTEN protein and are less prone to tumorigenesis. Reduction of OTUD3 expression, concomitant with decreased PTEN abundance, correlates with human breast cancer progression. Furthermore, we identified loss-of-function OTUD3 mutations in human cancers, which either abolish OTUD3 catalytic activity or attenuate the interaction with PTEN. These findings demonstrate that OTUD3 is an essential regulator of PTEN and that the OTUD3-PTEN signalling axis plays a critical role in tumour suppression.
Insights
Researchers identified OTUD3 as a deubiquitylase that stabilizes PTEN, a key tumor suppressor. Loss of OTUD3 promotes cancer progression and metastasis, highlighting the OTUD3-PTEN axis in tumor suppression.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- PTEN is a critical tumor suppressor frequently altered in cancer.
- While PTEN's ubiquitin ligases are known, its stabilizing deubiquitylase remains largely uncharacterized.
- Reduced PTEN protein stability contributes to tumorigenesis.
Purpose of the Study:
- To identify and characterize the deubiquitylase responsible for PTEN stabilization.
- To elucidate the role of this deubiquitylase in cancer development and progression.
Main Methods:
- Biochemical assays to confirm OTUD3's deubiquitylase activity on PTEN.
- In vitro and in vivo experiments assessing PTEN stability and Akt signaling.
- Analysis of OTUD3 expression and mutations in human cancer samples.
- Generation and analysis of OTUD3 transgenic mice.
Main Results:
- OTUD3 was identified as a deubiquitylase that directly interacts with and de-polyubiquitylates PTEN, enhancing its stability.
- OTUD3 depletion resulted in PTEN degradation, Akt pathway activation, cellular transformation, and metastasis.
- OTUD3 transgenic mice showed increased PTEN levels and resistance to tumorigenesis.
- Reduced OTUD3 expression and loss-of-function mutations in OTUD3 were correlated with human breast cancer progression.
Conclusions:
- OTUD3 is a crucial deubiquitylase that stabilizes PTEN, acting as a tumor suppressor.
- The OTUD3-PTEN signaling pathway is vital for maintaining tumor suppression.
- Dysregulation or mutation of OTUD3 contributes to human cancer development and progression.
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