CYTOTOXIC EFFECTS OF VITEXIN IN A549 HUMAN NON-SMALL CELL LUNG CANCER CELLS


Akalın Çiftçi G., Ertorun I., Hüseynli A., Karaca Arpa Ş.

8th INTERNATIONAL CONGRESS on APPLIED BIOLOGICAL SCIENCES , Priştine, Kosova, 13 - 16 Eylül 2023, ss.41

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Priştine
  • Basıldığı Ülke: Kosova
  • Sayfa Sayıları: ss.41
  • Anadolu Üniversitesi Adresli: Evet

Özet

Lung cancer ranks highest as the primary cause of cancer-related deaths globally. There are two primary categories of lung cancer: small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). NSCLC makes up about 85% of all lung cancer cases. Currently, the standard treatment options for NSCLC in medical practice are chemotherapy and surgery. However, these approaches have limited efficacy for patients diagnosed with advanced NSCLC. It is crucial to recognize the significance of discovering new therapeutic agents to effectively treat this deadly form of cancer. Recently, researchers have been increasingly interested in natural products and especially compounds derived from plants, which have a high potential to be anti-tumor agents. Vitexin (apigenin-8-C-glucoside), a flavonoid, is one of them. Vitexin has recently been known to have anti-cancer, antioxidant, anti inflammatory, anti-nociceptive, anti-hypertensive, anti-depressant-like effects and anti-viral activities. In this study, the anticancer effects of vitexin were investigated on the A549 human lung adenocarcinoma cell line. Cisplatin was evaluated as a positive control. Cytotoxicity and IC50 values of vitexin in A549 cells were determined by MTT assay. Various concentrations of vitexin (15.62-2000 μM) effectively reduced cell viability in A549 cell line in a dose-dependent manner. IC50 values of vitexin and cisplatin were determined as 186,67 μM and 29,11 μM in A549 cells for 24h respectively. In addition, early phase apoptosis and caspase 3 activity also increased in a time-dependent manner. This results show that vitexin had selective anticancer activity in A549 cell line.