Melatonin Exerts Anticancer Effects in Human Tongue Squamous Cell Carcinoma Cells by Promoting Autophagy
Eui-Suk Sung1, Joo-Young Kim2, Yong Tae Ahn3
1Department of Otolaryngology-Head and Neck Surgery, College of Medicine and Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
Background/Aim:
The global prevalence of head and neck squamous cell carcinoma (HNSCC) remains high, and its prognosis poor. We investigated the anticancer effects of melatonin in human tongue squamous cell carcinoma cells (SCC-25) and its mechanisms of action.
Materials And Methods:
MTT assay was used to determine cell viability. To assess the effects of melatonin on SCC-25 cell metastasis, we conducted cell formation, wound healing, transwell migration and invasion assay. Western blot analysis was performed to measure the levels of autophage marker proteins.
Results:
We found that melatonin treatment significantly reduced the viability and colony formation ability of SCC-25 cells, impairing cell migration and invasion. Western blotting assay revealed that melatonin increased the levels of autophagy markers, such as LC-3B and Beclin-1. Consequently, melatonin induces autophage in SCC-25 cells.
Conclusion:
Melatonin may be a promising anticancer agent for the treatment of human tongue squamous cell carcinoma.
Insights
Melatonin significantly reduced head and neck squamous cell carcinoma (HNSCC) cell viability and metastasis. This study shows melatonin induces autophagy, suggesting its potential as an anticancer agent for tongue cancer.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Head and neck squamous cell carcinoma (HNSCC) has a high global prevalence and poor prognosis.
- Investigating novel therapeutic strategies for HNSCC is crucial.
Purpose of the Study:
- To investigate the anticancer effects of melatonin on human tongue squamous cell carcinoma (SCC-25) cells.
- To elucidate the underlying mechanisms of melatonin's action, focusing on autophagy.
Main Methods:
- Cell viability was assessed using MTT assays.
- Cell migration and invasion were evaluated through wound healing and Transwell assays.
- Autophagy markers (LC-3B, Beclin-1) were quantified via Western blot analysis.
Main Results:
- Melatonin treatment significantly inhibited SCC-25 cell viability and colony formation.
- Melatonin impaired SCC-25 cell migration and invasion capabilities.
- Melatonin increased the expression of autophagy markers, indicating induced autophagy in SCC-25 cells.
Conclusions:
- Melatonin demonstrates significant anticancer effects against human tongue squamous cell carcinoma cells.
- Melatonin-induced autophagy plays a role in its cytotoxic effects.
- Melatonin holds promise as a potential therapeutic agent for tongue HNSCC.
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