Departamento de Química, Facultad de Ciencias, Universidad Nacional de Colombia, Bogotá, Carrera 45 No 26-85, Building 451, office 409, Bogotá 11321, Colombia.
Facultad de Medicina Veterinaria y Zootecnia, Centro Multidisciplinario de Estudios en Biotecnología, Universidad Michoacana de San Nicolás de Hidalgo, Km 9.5 Carretera Morelia-Zinapécuaro, Posta Veterinaria, P.C. 58893 Morelia, Michoacán, Mexico.
Int J Mol Sci. 2020 Jun 26;21(12):4550. doi: 10.3390/ijms21124550.
The effect on the cytotoxicity against breast cancer cell lines of the substitution of Met residue in the sequence of the Bovine Lactoferricin-derived dimeric peptide LfcinB (20-30): (RRWQWRMKKLG)-K- with amino acids of different polarity was evaluated. The process of the synthesis of the LfcinB (20-30) analog peptides was similar to the original peptide. The cytotoxic assays showed that some analog peptides exhibited a significant cytotoxic effect against breast cancer cell lines HTB-132 and MCF-7, suggesting that the substitution of the Met with amino acids of a hydrophobic nature drastically enhances its cytotoxicity against HTB-132 and MCF-7 cells, reaching IC values up to 6 µM. In addition, these peptides have a selective effect, since they exhibit a lower cytotoxic effect on the non-tumorigenic cell line MCF-12. Interestingly, the cytotoxic effect is fast (90 min) and is maintained for up to 48 h. Additionally, through flow cytometry, it was found that the obtained dimeric peptides generate cell death through the apoptosis pathway and do not compromise the integrity of the cytoplasmic membrane, and there are intrinsic apoptotic events involved. These results show that the obtained peptides are extremely promising molecules for the future development of drugs for use against breast cancer.
本研究评价了在牛乳铁蛋白衍生二聚肽 LfcinB(20-30)序列中(RRWQWRMKKLG)-K-的 Met 残基被不同极性氨基酸取代对乳腺癌细胞系的细胞毒性的影响。LfcinB(20-30)类似肽的合成过程与原始肽相似。细胞毒性测定表明,一些类似肽对乳腺癌细胞系 HTB-132 和 MCF-7 表现出显著的细胞毒性作用,这表明用疏水性氨基酸取代 Met 大大增强了其对 HTB-132 和 MCF-7 细胞的细胞毒性,达到 IC 值高达 6µM。此外,这些肽具有选择性作用,因为它们对非致瘤细胞系 MCF-12 的细胞毒性作用较低。有趣的是,细胞毒性作用迅速(90 分钟),并能维持长达 48 小时。此外,通过流式细胞术发现,获得的二聚肽通过凋亡途径诱导细胞死亡,且不损害细胞质膜的完整性,并涉及内在的凋亡事件。这些结果表明,获得的肽是未来开发用于治疗乳腺癌的药物的极有前途的分子。