Genotoxic effects of BnSP-6, a Lys-49 phospholipase A2 (PLA2) homologue from Bothrops pauloensis snake venom, on MDA-MB-231 breast cancer cells

被引:23
|
作者
Silva, Makswell Almeida [1 ]
Lopes, Daiana Silva [1 ]
Teixeira, Samuel Cota [2 ]
Cirilo Gimenes, Sarah Natalie [1 ]
Vasconcelos Azevedo, Fernanda Van Petten [1 ]
Polloni, Lorena [3 ]
Borges, Bruna Cristina [4 ]
da Silva, Marcelo Santos [5 ]
Barbosa, Marcelo Jose [4 ]
de Oliveira Junior, Robson Jose [3 ]
Elias, Maria Carolina [5 ]
da Silva, Claudio Vieira [2 ]
Geraldo Yoneyama, Kelly Aparecida [1 ]
Rodrigues, Veridiana de Melo [1 ]
Rodrigues, Renata Santos [1 ]
机构
[1] Univ Fed Uberlandia, UFU, Inst Biotechnol, Lab Biochem & Anim Toxins, Uberlandia, MG, Brazil
[2] Univ Fed Uberlandia, Biomed Sci Inst, Dept Immunol, Lab Trypanosomatids,UFU, Uberlandia, MG, Brazil
[3] Univ Fed Uberlandia, Genet & Biochem Inst, Lab Cytogenet Anim, UFU, Uberlandia, MG, Brazil
[4] Univ Fed Uberlandia, Biomed Sci Inst, Lab Tumor Biomarkers & Osteoimmunol, UFU, Uberlandia, MG, Brazil
[5] Butantan Inst, Ctr Toxins Immune Response & Cell Signaling CeTIC, Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
PIA(2); BnSP-6; Breast cancer; Genotoxicity; Cell cycle; Bothrops pauloensis; FACTOR-KAPPA-B; OXIDATIVE STRESS; CYCLE ARREST; BIOLOGICAL-ACTIVITY; CRYSTAL-STRUCTURE; ISOLATED TOXINS; HEPG2; CELLS; DNA-DAMAGE; APOPTOSIS; PROGRESSION;
D O I
10.1016/j.ijbiomac.2018.06.082
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Herein we evaluated the genotoxic effects of BnSP-6, a Lys-49 phospholipase A(2) (PLA(2)) 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 (GI) 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. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:311 / 319
页数:9
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