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FOXD1-mTOR Signaling Pathway on Oral Squamous Cell Carcinoma and Its Inhibition by Rosemary Extract (Invitro-Study)
Yasmine Alaa El-Din1, Dina Sabry2,3, Sahar H Ahmed4
1Oral and Maxillofacial Pathology, Faculty of Dentistry, October 6 University, Cairo, Egypt.
Background:
FOXD1 expression in oral squamous cell carcinoma remains uncovered. The aim was to detect the anticancer effect of Rosemary Extract RE through the evaluation of FOXD1 gene expression in (OSCC) by quantitative PCR.
Methods:
OSCC cell line was served as a control group. Moreover, the OSCC cell line (SCC-15) was treated with RE (OSCC/ RE group) at 24, 48, and 72 hs time intervals. We assessed the antioxidant activity of RE by evaluation of lipid peroxidation (MDA) and superoxide dismutase (SOD) levels. The cytotoxic effects of RE were examined by MTT assay. mTOR and LC3 I/II autophagy protein markers were assessed by western blot. Apoptosis activity was assessed.
Results:
The study results were statistically assessed. Intergroup comparisons were analyzed, whereas intragroup comparisons were conducted utilizing one-way repeated measures ANOVA, followed by multiple pairwise paired t-tests with Bonferroni correction revealed a significant increase of FOXD1 gene expression in the control OSCC group in comparison to the OSCC/RE group (p-value <0.001). A significant decrease of mTOR/LC3I/II proteins expression in the OSCC/RE group compared to the control OSCC group (p-value <0.001).
Conclusion:
FOXD1 can be considred a diagnostic biomarker for OSCC. RE inhibits autophagy of oral human cancer cells via mTOR/LC3I/II-dependent pathways and decrease caspase -3 apoptotic level.
Insights
Rosemary extract (RE) significantly reduces oral squamous cell carcinoma (OSCC) growth by decreasing FOXD1 gene expression and inhibiting autophagy via mTOR/LC3 pathways. This suggests RE
Area of Science:
- Oncology
- Molecular Biology
- Natural Product Chemistry
Background:
- The role of FOXD1 gene expression in oral squamous cell carcinoma (OSCC) is largely unknown.
- Investigating natural compounds for anticancer properties is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To evaluate the anticancer effects of Rosemary Extract (RE) on OSCC.
- To determine the impact of RE on FOXD1 gene expression in OSCC.
- To explore the mechanisms of RE's action, including autophagy and apoptosis.
Main Methods:
- Quantitative PCR was used to measure FOXD1 gene expression.
- Cell viability was assessed using MTT assay.
- Western blot analysis was performed to evaluate autophagy markers (mTOR, LC3 I/II) and apoptosis.
- Antioxidant activity was measured by lipid peroxidation (MDA) and superoxide dismutase (SOD) levels.
Main Results:
- Rosemary Extract significantly decreased FOXD1 gene expression in OSCC cells (p < 0.001).
- RE treatment led to a significant reduction in mTOR and LC3 I/II protein levels, indicating autophagy inhibition (p < 0.001).
- RE demonstrated cytotoxic effects and modulated apoptosis markers.
Conclusions:
- FOXD1 may serve as a diagnostic biomarker for OSCC.
- Rosemary Extract inhibits autophagy in oral cancer cells through mTOR/LC3-dependent pathways.
- RE exhibits anticancer potential by affecting autophagy and apoptosis in OSCC.
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