article = {COR-2020-2-103} title = {Cytotoxicity of SH-SY5Y Neuroblastoma Cells to the Antipsychotic Drugs, Chlorpromazine and Trifluoperazine, is via a Ca2+ -Mediated Apoptosis Process and Differentiation of These Cells with Retinoic Acid Makes Them More Resistant to Cell Death} journal = {Clinical Oncology and Research} year = {2020} issn = {2613-4942} doi = {http://dx.doi.org/10.31487/j.COR.2020.02.03} url = {https://www.sciencerepository.org/cytotoxicity-of-sh-sy5y-neuroblastoma-cells-to-the-antipsychotic-drugs_COR-2020-2-103 author = {Francesco Mongelli,Israa J. Hakeem ,Nikolas J Hodges ,} keywords = {Antipsychotic drugs, chlorpromazine, trifluoperazine, SH-SY5Y cells, retinoic acid, differentiated} abstract ={Neuroblastomas usually occur in childhood and can have a relatively poor prognosis. Additionally, some antipsychotic drugs have been suggested to be neurotoxic, suggesting they might have therapeutic potential against neuronal cancer cells. In this study it was shown that 7 days treatment with 10 µM all-trans retinoic acid (ATRA) could alter SH-SY5Y (an undifferentiated neuroblastoma cell line) morphology in terms of neurite outgrowths and increased expression of the growth associated protein (GAP43), thus indicating that ATRA-treatment made these cells more differentiated in character. Next, a comparison of the effects of chlorpromazine and trifluoperazine, two types of typical first-generation antipsychotic drugs, on the cytotoxicity of both undifferentiated and ATRA-differentiated SH-SY5Y cells was undertaken. The results showed that both chlorpromazine and trifluoperazine, were highly cytotoxic to undifferentiated SH-SY5Y cells (LC50 values 5µM and 6µM, respectively). They were also deemed to be more selective towards neuronal cells compared to non-neuronal cells (COS7 cells). it was shown that cell death induced by chlorpromazine and trifluoperazine occurred mostly by Ca2+-mediated apoptosis. Furthermore, the cytotoxicity of chlorpromazine and trifluoperazine was decreased when the cells were differentiated with ATRA (LC50 values of 10.5µM and 12µM, respectively), indicating a possible therapeutic window for the potential use of chlorpromazine and trifluoperazine and potentially other FGAs in the treatment of neuroblastomas.}