Abstract
Objective:Apoptosis, which is a programmed cell death, is an event in which cells destroy themselves without inflammation, as well as requiring energy and homeostasis is preserved. In cases where apoptosis slows down, autoimmune diseases and cancer occur. Aspirin is a salicylic ester of acetic acid and has analgesic, anti-inflammatory, antipyretic and antithrombotic effects. In this study, we investigated the effects of aspirin on apoptosis in human neuroblastoma SK-N-MC cell line in vitro.Methods:In our study, trypan blue viability test (Tyripan Blue Exclusion) method was used for aspirin doses to be given to the cells. The apoptotic effect of aspirin in the SK-N-MC cell line was determined by flow cytometry imaging using APC Anexin V antibody.Results: The aspirin was incubated in SK-N-MC cells at concentrations of 10-100μM, and measurements at 24 and 48 hours were recorded. According to trypan blue results, cell density decreased proportionally with increasing aspirin concentration compared to the control group. The cytotoxic dose was found to be between 50-80 μM at the 24th hour and 70 μM at the 48th hour.Anexin V flow cytometry measurement results showed that 60 and 70 μM aspirin given to SK-N-MC cells increased early apoptosis compared to control group.Conclusion:The results of our study showed that aspirin inducedapoptosis in SK-N-MC cells in vitrodepending on dose and time.