Parasporin A13-2 of <i>Bacillus thuringiensis</i> Isolates from the Papaloapan Region (Mexico) Induce a Cytotoxic Effect by Late Apoptosis against Breast Cancer Cells

• Main Authors: Diego Becker Borin, Karen Castrejón-Arroyo, Alain Cruz-Nolasco, Miguel Peña-Rico, Michele Rorato Sagrillo, Roberto C. V. Santos, Lucas Silva de Baco, Lemuel Pérez-Picaso, Luz Camacho, A. Karin Navarro-Mtz
• Format: Article
• Language: English
• Published: MDPI AG 2021-07-01
• Series: Toxins
• Subjects: parasporins; anticancer; cytotoxicity; late apoptosis; MCF-7
• Online Access: https://www.mdpi.com/2072-6651/13/7/476

The protein A13-2 was obtained from <i>Bacillus thuringiensis</i> strains isolated from the Papaloapan watershed region (Oaxaca, Mexico). The cytotoxic activity of parasporal inclusions was studied against breast cancer cell line (MCF-7) and normal cell (human peripheral blood mononuclear cells). The MTT, the formation of reactive species, nitric oxide, free cell DNA, and the type of death cellular were assessed. The protein A13-2 shows the highest cytotoxic activity against MCF-7 (13% cell viability at 6 µg/mL), the extracellular DNA increases, and it shows no stress for reactive species or nitric oxide. Besides, the A13-2 parasporin shows no toxicity to peripheral blood mononuclear cells, and it does not generate changes in nitric oxide levels or free cell DNA. Due to that, the cytotoxic effect of A13-2 was specific for MCF-7, and it does not affect normal cells. According to microscopy and flow cytometry, A13-2 parasporin leads to the death of MCF-7 cells by late apoptosis together with necrosis and without allowing the triggering of the survival mechanisms. When analyzed together, our results show for the first time that the A13-2 protein isolated from Mexican strains of <i>B. thuringiensis</i> preferentially kills MCF- 7 (cancer cells) over HEK 293 and PBMC cell lines (normal cells), thus representing a promising alternative for the treatment of cancer breast.