Laboratory of Biochemistry and Animal Toxins, Institute of Biotechnology, Federal University of Uberlandia, UFU, Uberlandia, MG, Brazil.
Laboratory of Trypanosomatids, Department of Immunology, Biomedical Sciences Institute, Federal University of Uberlandia, UFU, Uberlandia, MG, Brazil.
Int J Biol Macromol. 2018 Oct 15;118(Pt A):311-319. doi: 10.1016/j.ijbiomac.2018.06.082. Epub 2018 Jun 18.
Herein we evaluated the genotoxic effects of BnSP-6, a Lys-49 phospholipase A (PLA) from Bothrops pauloensis, on breast cancer cells. BnSP-6 was able to induce a higher cytotoxic and genotoxic activity in MDA-MB-231 cells, when compared to MCF10A (a non-tumorigenic breast cell line), suggesting that this protein presented a possible preference for cancer cells. BnSP-6 inhibited MDA-MB-231 proliferation at 24, 48 and 72 h. In addition, BnSP-6 induced significant increase in the percentage of TUNEL-positive cells, a marker of DNA damage. To obtain novel insight into the direct DNA damage interference in MDA-MB-231 survival and proliferation, we evaluated cell cycle progression. BnSP-6 produced a significant decrease in 2N (G1) and an increase in the G2/M phase and this capacity is likely related to the modulation of expression of progression cell cycle-associated genes (CCND1, CCNE1, CDC25A, CHEK2, E2F1, CDH-1 and NF-kB). Taken together, these results indicate that BnSP-6 induces DNA damage in breast cancer cells and is an attractive model for developing innovative therapeutic agents against breast cancer.
本文评估了来自矛头蝮蛇(Bothrops pauloensis)的 Lys-49 磷脂酶 A(PLA)BnSP-6 对乳腺癌细胞的遗传毒性作用。与 MCF10A(非致瘤性乳腺细胞系)相比,BnSP-6 能够诱导 MDA-MB-231 细胞产生更高的细胞毒性和遗传毒性活性,这表明该蛋白可能对癌细胞具有偏好性。BnSP-6 在 24、48 和 72 小时抑制 MDA-MB-231 的增殖。此外,BnSP-6 诱导 TUNEL 阳性细胞(DNA 损伤标志物)的百分比显著增加。为了深入了解 BnSP-6 对 MDA-MB-231 存活和增殖的直接 DNA 损伤干扰,我们评估了细胞周期进程。BnSP-6 导致 2N(G1)显著减少,G2/M 期增加,这种能力可能与调节与细胞周期进展相关的基因(CCND1、CCNE1、CDC25A、CHEK2、E2F1、CDH-1 和 NF-kB)的表达有关。综上所述,这些结果表明 BnSP-6 诱导乳腺癌细胞的 DNA 损伤,是开发针对乳腺癌的创新治疗药物的有吸引力的模型。