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Updated: Apr 30, 2026

Profiling of Estrogen-regulated MicroRNAs in Breast Cancer Cells
Published on: February 21, 2014
Research progress of DUB enzyme in breast cancer
Wei Tang1, Ning Li2, Jianjun Lai3
1Department of Breast and Thyroid Surgery, Feicheng People's Hospital, Taian, 271600, China.
Abstract:
According to GLOBOCAN 2022 cancer incidence and mortality statistics compiled by the International Agency for Research on Cancer, the incidence rate of breast cancer (BC) ranks second among all 36 types of cancers, just after lung cancer. Despite great advances in breast cancer (BC) treatment-including agents such as Tamoxifen, Fulvestrant, Toremifene, and Raloxifene, all of which are approved for the systemic treatment of BC patients-these agents only prolong survival by a few months, and patients with advanced BC remain susceptible to drug resistance. Ubiquitination, a type of post-translational protein modification, influences cellular physiological activities by regulating protein localization, stability, and activity in pathways such as gene transcription and DNA damage signaling. The reversible process of ubiquitination, termed deubiquitination, refers to the release of ubiquitinated substrates through the action of deubiquitinases (DUBs) and other active molecules. In breast cancer, an increasing number of DUBs have been identified to exhibit aberrant expression, with specific DUBs capable of either promoting or suppressing mammary tumorigenesis depending on their substrates. In this review, we focused on several DUBs associated with breast cancer, including their structure, function, and relationship to BC. Among them, we focused on the USP family and OTU family, which are more extensively studied in BC.
Insights
Deubiquitinases (DUBs) play a crucial role in breast cancer (BC) progression and drug resistance. Understanding DUBs, particularly USP and OTU families, offers new therapeutic targets for advanced breast cancer.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Breast cancer (BC) is the second most common cancer globally, with advanced stages facing significant drug resistance.
- Current treatments offer limited survival benefits for advanced BC patients.
- Ubiquitination, a key post-translational modification, regulates protein stability and cellular processes, and its dysregulation is implicated in cancer.
Purpose of the Study:
- To review the role of deubiquitinases (DUBs) in breast cancer.
- To explore the structure, function, and aberrant expression of DUBs in BC.
- To highlight specific DUB families, USP and OTU, in the context of breast cancer.
Main Methods:
- Literature review of DUBs in breast cancer.
- Analysis of DUBs' involvement in tumorigenesis and drug resistance.
- Focus on USP and OTU families based on existing research.
Main Results:
- Aberrant DUB expression is common in breast cancer, with some DUBs promoting and others suppressing tumor growth.
- DUBs influence critical pathways like gene transcription and DNA damage signaling.
- Specific DUBs, including those in the USP and OTU families, are significantly associated with breast cancer development and progression.
Conclusions:
- Deubiquitinases represent promising therapeutic targets for overcoming drug resistance in advanced breast cancer.
- Further research into DUBs' functions and substrates is crucial for developing novel BC treatments.
- Targeting specific DUB families like USP and OTU may offer new strategies for breast cancer therapy.
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