Anti-proliferative and immunomodulatory properties of kaffir lime leaves and bioactive compounds on macrophages co-cultured with squamous cell carcinoma.
Thitiya LuetragoonYordhathai ThongsriKrai DaotakPachuen PotupKanchana UsuwanthimPublished in: PloS one (2023)
Head and neck squamous cell carcinoma (HNSCC) is the seventh most common cancer worldwide. Late-stage patients have a significant chance of local recurrence and distant metastasis, as well as poor prognosis. Therapeutic goals for patients must be improved and personalized to reduce adverse effects. This study explored the anti-proliferative activity and immunomodulation potential of the constituents of crude kaffir lime leaf extract (lupeol, citronellal and citronellol) under co-culture. Results showed high cytotoxicity to human SCC15 cell line but not to human monocyte-derived macrophages. Treatment with crude extract and the contained compounds also suppressed cell migration and colony formation of SCC15 compared to the untreated control group, while high levels of intracellular ROS production were detected in the treatment group of SCC15. The MuseTM cell analyzer revealed cell cycle arrest at G2/M phase and apoptosis induction. Inhibition of Bcl-2 and activation of Bax, leading to induction of the downstream caspase-dependent death pathway were confirmed by Western blot analysis. Co-culture with activated macrophages, kaffir lime extract and its constituents enhanced the development of pro-inflammatory (M1) macrophages and boosted TNF-α production, resulting in SCC15 apoptosis. Findings revealed novel potential activities of kaffir lime leaf extracts and their constituents in inducing M1 polarization against SCC15, as well as direct anti-proliferative activity.
Keyphrases
- cell cycle arrest
- cell death
- poor prognosis
- endothelial cells
- squamous cell carcinoma
- oxidative stress
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- cell migration
- prognostic factors
- endoplasmic reticulum stress
- stem cells
- dna damage
- reactive oxygen species
- patient reported outcomes
- induced apoptosis
- radiation therapy
- signaling pathway
- climate change
- south africa
- essential oil
- cell proliferation
- smoking cessation
- replacement therapy
- rectal cancer