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Published on: August 2, 2024
RUNX3 functions as an oncogene in ovarian cancer
Cecilia Wei Lin Lee1, Linda Shyue Huey Chuang, Shunichi Kimura
1Cancer Science Institute of Singapore, National University of Singapore, Singapore.
Objective:
The Runt domain transcription factor, RUNX3, has been shown to be a tumor suppressor in a variety of cancers including gastric, colon and breast cancer. Interestingly, an oncogenic role for RUNX3 has also been suggested in basal cell carcinoma and head and neck cancer. Here, we explore the role of RUNX3 in ovarian cancer.
Methods:
Expression of RUNX3 mRNA and protein was evaluated in human ovarian cancer cell lines. In addition, subcellular localization of RUNX3 was also examined in cell lines and ovarian cancer tissues. Effect of exogenous RUNX3 expression and knockdown on cell proliferation was investigated by proliferation assays and a soft agar assay.
Results:
Expression of RUNX3 was detected in the nucleus of ovarian cancer cell lines and ovarian cancer tissues and was found to play a growth stimulatory role. RUNX3 knockdown resulted in a decrease in cell proliferation in liquid media as well as in soft agar. Despite the fact that exogenous expression of RUNX3 strongly inhibits cell growth in many cell types, RUNX3 promoted cell growth in ovarian cancer cell lines not expressing RUNX3.
Conclusion:
RUNX3 is frequently expressed in the nuclei of ovarian cancer cell lines and plays an oncogenic role in ovarian cancer.
Insights
RUNX3 acts as an oncogene in ovarian cancer, promoting cell growth. Its nuclear expression in ovarian cancer cells indicates a potential therapeutic target for this disease.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- RUNX3 (Runt domain transcription factor 3) exhibits context-dependent roles in cancer, acting as a tumor suppressor in some cancers and an oncogene in others.
- Previous studies have indicated both tumor-suppressive and oncogenic functions for RUNX3 across various cancer types.
Purpose of the Study:
- To investigate the specific role of RUNX3 in the development and progression of ovarian cancer.
- To determine if RUNX3 acts as a tumor suppressor or oncogene in ovarian cancer.
Main Methods:
- Assessed RUNX3 mRNA and protein expression in ovarian cancer cell lines and tissues.
- Examined the subcellular localization of RUNX3.
- Investigated the impact of RUNX3 modulation (expression and knockdown) on ovarian cancer cell proliferation using proliferation assays and soft agar assays.
Main Results:
- RUNX3 was detected in the nucleus of ovarian cancer cell lines and tissues, suggesting nuclear localization is important for its function.
- RUNX3 knockdown significantly decreased ovarian cancer cell proliferation in both liquid culture and soft agar assays.
- Exogenous expression of RUNX3 promoted cell growth in ovarian cancer cell lines that did not initially express RUNX3, contrasting its known tumor-suppressive role in other cell types.
Conclusions:
- RUNX3 is frequently expressed in the nucleus of ovarian cancer cells.
- RUNX3 plays a significant oncogenic role in ovarian cancer, promoting tumor cell proliferation.
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