Apoptotic Effects Of Androctonus Crassicauda Crude Venom On Mda-Mb-231 TripleNegative Breast Cancer Cells


Sabah B. N., Mergen H., Toprak Ş., Açık L.

International Congress of Medical and Health Sciences, Şanlıurfa, Türkiye, 23 - 24 Ocak 2026, ss.440-441, (Özet Bildiri)

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Şanlıurfa
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.440-441
  • Gazi Üniversitesi Adresli: Evet

Özet

Cell death is a critical cellular process in the developmental process, crucial for organ formation and maintaining tissue homeostasis. Apoptosis, a type of programmed cell death, plays a role in maintaining tissue integrity by eliminating unnecessary or damaged cells. Disruption of apoptotic mechanisms can lead to uncontrolled cell proliferation and cancer development. Therefore, natural or synthetic compounds targeting apoptosis are among the important research areas for cancer treatment. Biotoxins are natural compounds produced by various organisms that have pharmacological potential. Scorpion venoms, which are biotoxin derivatives, are reported to exhibit anti-tumor effects due to containing bioactive molecules that can induce apoptosis.

This study aimed to investigate the cytotoxic and apoptotic effects of raw venom from the scorpion species Androctonus crassicauda (Olivier, 1807) on MDA-MB-231 triple-negative breast cancer and Vero healthy cell lines. Cell viability was assessed using the MTT method, and changes in mitochondrial membrane potential were analyzed using fluorescent staining. Expression levels of apoptosis-related genes (CASP3, CDKN1A, TP53, NOXA, PUMA, BCL2, BCL2L1, and BAX) were determined using the RT-qPCR method.

The findings showed that raw scorpion venom significantly reduced cell viability in breast cancer cells depending on the concentration (p<0.0001). While raw scorpion venom showed a significant cytotoxic effect in MDA-MB-231 breast cancer cells, it did not cause significant toxicity in healthy cells. This finding reveals that the venom exhibits selective toxicity against cancer cells. A significant decrease in mitochondrial membrane potential was observed 24 hours after venom application to breast cancer cells. Gene expression analyses revealed significant decreases in CASP3 and CDKN1A genes, and significant increases in PUMA and pro-apoptotic BAX genes (p<0.05).

In conclusion, it is thought that A. crassicauda venom exhibits anti-tumor effects by inducing apoptosis in MDA-MB-231 triple-negative breast cancer cells and may be a potential therapeutic agent for diseases associated with cell death.

Keywords: Scorpion Venom; Apoptosis; Biotoxin; Cell Death; Breast Cancer