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Published on: September 1, 2019
Oncogenic role of RUNX3 in head and neck cancer
Yasusei Kudo1, Takaaki Tsunematsu, Takashi Takata
1Division of Frontier Medical Science, Department of Oral and Maxillofacial Pathobiology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan. ykudo@hiroshima-u.ac.jp
Abstract:
Cumulative evidences show that Runt-related transcription factor 3 (RUNX3) has a tumor suppressive role in various cancers. In particular, RUNX3 appears to be an important component of the transforming growth factor-β (TGF-β)-induced tumor suppression pathway. Contrary to reports on this tumor suppressive role of RUNX3, RUNX3 can also function as an oncogene when overexpressed. Recently, we found that RUNX3 overexpression was frequently observed and was well correlated with malignant behaviors in head and neck cancer, which is one of the most common types of human cancer. Moreover, it has been revealed that RUNX3 overexpression promoted cell growth and inhibited apoptosis in head and neck cancer cells. This review introduces the oncogenic role of RUNX3 in certain types of cancer including head and neck cancer.
Insights
Runt-related transcription factor 3 (RUNX3) typically suppresses tumors but can act as an oncogene when overexpressed. In head and neck cancer, RUNX3 overexpression promotes malignancy by increasing cell growth and inhibiting apoptosis.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Runt-related transcription factor 3 (RUNX3) is recognized for its tumor-suppressive functions in various cancers.
- RUNX3 is a key player in the transforming growth factor-β (TGF-β)-mediated tumor suppression pathway.
- However, RUNX3 can exhibit oncogenic properties when its expression is elevated.
Purpose of the Study:
- To review the dual role of RUNX3 in cancer, focusing on its oncogenic function.
- To highlight the specific role of RUNX3 overexpression in head and neck cancer.
- To discuss the implications of RUNX3 as an oncogene in malignant behaviors.
Main Methods:
- Literature review of studies investigating RUNX3 in cancer.
- Analysis of evidence linking RUNX3 expression levels to tumor behavior.
- Examination of molecular mechanisms underlying RUNX3's oncogenic activity.
Main Results:
- RUNX3 overexpression is frequently observed in head and neck cancer.
- Elevated RUNX3 levels correlate with malignant characteristics in these tumors.
- RUNX3 overexpression enhances cell proliferation and suppresses apoptosis in head and neck cancer cells.
Conclusions:
- RUNX3 can function as an oncogene, particularly in head and neck cancer.
- RUNX3 overexpression contributes to tumor progression by promoting cell growth and inhibiting cell death.
- Understanding RUNX3's oncogenic role is crucial for developing targeted cancer therapies.
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