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Published on: December 26, 2016
Shugoshin 1 expression in various cancers: a potential target for therapy
Indumathi Ankathatti Narayanaswamy1, Abhay Kumaraswamy Kattepur2, Kalyani Raju3
1Department of Cell Biology and Molecular Genetics, Sri Devaraj Urs Academy of Higher Education and Research (Deemed to be University), Kolar, Karnataka, 563 103, India.
Shugoshin 1 (SGO1) is highly expressed in many cancers, promoting proliferation and metastasis. Targeting SGO1 with siRNA/shRNA effectively reduces cancer growth and increases sensitivity to chemotherapy.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Shugoshin 1 (SGO1) is crucial for centromere protection and chromosome segregation during cell division.
- Altered SGO1 expression is linked to various cancers and genetic disorders, indicating its therapeutic potential.
Purpose of the Study:
- To review the literature on SGO1 gene and protein expression in diverse cancer models.
- To evaluate the efficacy of targeting SGO1 using siRNA/shRNA in cancer therapy.
Main Methods:
- Literature review of SGO1 expression in cancer cell lines, animal models, and patient tissues.
- Analysis of SGO1 targeting using small interfering RNA (siRNA) and short hairpin RNA (shRNA).
Main Results:
- Elevated SGO1 mRNA and protein levels were observed across multiple cancer types (prostate, renal, lung, breast, etc.), correlating with increased proliferation, invasion, and metastasis.
- SGO1 knockout/haploinsufficiency in mice led to chromosome instability and tumorigenesis.
- Higher SGO1 expression in patient tumors correlated with advanced stage, grade, size, and hormonal status, and was associated with chemoresistance.
- SGO1 knockdown via siRNA/shRNA reduced cancer cell proliferation, induced apoptosis, and enhanced sensitivity to chemotherapeutic agents.
Conclusions:
- SGO1 is significantly upregulated in various cancers, acting as a driver of tumor progression.
- Targeting SGO1 with siRNA/shRNA represents a promising therapeutic strategy to inhibit cancer growth, metastasis, and overcome chemoresistance.
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