Luteolin (LUT) Induces Apoptosis and Regulates Mitochondrial Membrane Potential to Inhibit Cell Growth in Human Cervical Epidermoid Carcinoma Cells (Ca Ski)

• Published in: Biomedicines 2024-10, Vol.12 (10), p.2330
• Main Authors: Pei, Sung-Nan, Lee, Kuan-Ting, Rau, Kun-Ming, Lin, Tsung-Ying, Tsai, Tai-Hsin, Hsu, Yi-Chiang
• Format: Article
• Language: English
• Subjects: Annexin V; Antibodies; Apoptosis; Apoptosis-inducing factor; caspase activation; Caspase-3; Cell cycle; Cell growth; Cell proliferation; Cell viability; Cervical cancer; Cervical carcinoma; cervical epidermoid cancer; Data analysis; Flavonoids; Flow cytometry; Human papillomavirus; luteolin; Membrane potential; Membranes; Mitochondria; mitochondrial; R&D; Research & development; Software; Statistical analysis; Tumors; Western blotting; Womens health
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines12102330

Luteolin (LUT) is a natural flavonoid with known anti-inflammatory, antioxidant, and anti-cancer properties. Cervical cancer, particularly prevalent in certain regions, remains a significant health challenge due to its high recurrence and poor response to treatment. This study aimed to investigate the anti-tumor effects of LUT on human cervical epidermoid carcinoma cells (Ca Ski), focusing on cell growth inhibition, apoptosis induction, and regulation of mitochondrial membrane potential. Ca Ski cells were treated with varying concentrations of LUT (0, 25, 50, 100 µM) for different time periods (24, 48, 72 hours). Cell viability was measured using the MTT assay, apoptosis was assessed by flow cytometry with annexin V-FITC/PI staining, and changes in mitochondrial membrane potential were evaluated using JC-1 staining. Caspase-3 activation was examined by flow cytometry, and expression of apoptosis-related proteins (caspase-3, -8, -9, AIF) was analyzed via Western blotting. LUT significantly inhibited the growth of Ca Ski cells in a dose- and time-dependent manner, with the most pronounced effects observed at 100 µM over 72 hours. Flow cytometry confirmed that LUT induced apoptosis without causing necrosis. Mitochondrial membrane potential was reduced after LUT treatment, coinciding with increased caspase-3 activation. Western blot analysis revealed the upregulation of pro-apoptotic proteins caspase-3, -8, -9, and AIF, indicating that LUT induces apoptosis through the intrinsic mitochondrial pathway. Luteolin effectively inhibits cervical cancer cell proliferation and induces apoptosis by disrupting mitochondrial membrane potential and activating caspases. These findings suggest that LUT holds potential as a therapeutic agent for cervical cancer, with further studies needed to explore its in vivo efficacy and broader clinical applications.