Three snake venoms from Bothrops genus induced apoptosis and cell cycle arrest in K562 human leukemic cell line

• Published in: Toxicon (Oxford) Vol. 238; p. 107547
• Main Authors: Marinho, Aline D, Lucena da Silva, Emerson, Jullyanne de Sousa Portilho, Adrhyann, Lacerda Brasil de Oliveira, Laís, Cintra Austregésilo Bezerra, Emanuel, Maria Dias Nogueira, Beatriz, Leitão-Araújo, Moema, Lúcia Machado-Alves, Maria, Correa Neto, Carlos, Seabra Ferreira, Jr, Rui, de Fátima Aquino Moreira-Nunes, Caroline, Elisabete Amaral de Moraes, Maria, Jorge, Roberta J B, Montenegro, Raquel C
• Format: Journal Article
• Language: English
• Published: England 01-02-2024
• Subjects: Cytotoxicity; Bothrops snake venom; K562 human cancer cell line; Chronic myeloid leukemia; Apoptosis
• ISSN: 0041-0101; 1879-3150
• DOI: 10.1016/j.toxicon.2023.107547

Cancer is indisputably one of the leading causes of death worldwide. Snake venoms are a potential source of bioactive compounds, complex mixtures constituted mainly of proteins and peptides with several pharmacological possibilities, including the potential to inhibit tumoral cell growth. In the present study, it was evaluated the antitumor effect of crude venom of Bothrops erythromelas (BeV), Bothrops jararaca (from Southern and Southeastern- BjsV and BjsdV, respectively) and Bothrops alternatus (BaV) in in vitro Chronic myeloid leukemia (CML) cancer cell line model. After 24 h of cell exposure to 10 and 50 μg/mL, BjsV, BjsdV, and BaV exerted a decrease in cell viability in both concentrations. BeV was not cytotoxic and, therefore wasn't chosen for further mechanism of action investigation. Furthermore, morphological alterations show modification typical of apoptosis. Also, was observes a significant cell cycle arrest in the S phase by BjsdV and BaV treatment. Flow cytometry evidenced the involvement of changes in the cell membrane permeability and the mitochondrial function by BjsV and BjsdV, corroborating with the triggering of the apoptotic pathway by the venom administration. BjsV, BjsdV, and BaV also led to extensive DNA damage and were shown to modulate the gene expression of transcripts related to the cell cycle progression and suppress the expression of the BCR-ABL1 oncogene. Altogether, these findings suggest that the venoms trigger the apoptosis pathway due to mitochondrial damage and cell cycle arrest, with modulation of intracellular pathways important for CML progression. Thus, indicating the pharmacological potential of these venoms in the development of new antitumoral compounds.