Miceli Rebecca T, Allen Noah G, Subramaniam Bhagyashree, Carmody Livia, Dordick Jonathan S, Corr David T, Cotten Myriam, Gross Richard A
Department of Chemistry and Chemical Biology, Rensselaer Polytechnic Institute, Troy, New York 12180, United States.
Center for Biotechnology and Interdisciplinary Sciences, Rensselaer Polytechnic Institute, Troy, New York 12180, United States.
ACS Omega. 2024 Jul 24;9(31):33408-33424. doi: 10.1021/acsomega.3c09902. eCollection 2024 Aug 6.
Piscidin 3 (P3), a peptide produced by fish, and a hexyl ester-modified sophorolipid (SL-HE), have individually shown promise as antimicrobial and anticancer drugs. A recent report by our team revealed that combining P3 with SL-HE in a 1:8 molar ratio resulted in an 8-fold enhancement in peptide activity, while SL-HE improved by 25-fold its antimicrobial activity against the Gram-positive microorganism . Extending these findings, the same P3/SL-HE combination was assessed on two breast cancer cell lines: BT-474, a hormonally positive cell line, and MDA-MB-231, an aggressive triple-negative cell line. The results demonstrated that the 1:8 molar ratio of P3/SL-HE synergistically enhances the anticancer effects against both tumorigenic breast cell lines. Mechanistic studies indicate the activation of an intrinsic apoptotic cell death mechanism through an increase in reactive oxygen species and mitochondrial dysfunction and a secondary programmed necrotic pathway that involves pore formation in the plasma membrane. When a fibroblast cell line, CCD1065SK HDF, was utilized to determine selectivity, the synergistic SL-HE/P3 combination exhibited a protective property compared to the use of SL-HE alone and therefore afforded vastly improved selectivity indices. Given the promising results reported herein, the synergistic combination of P3/SL-HE constitutes a novel strategy that merits further study for the treatment of breast cancer.
鱼源抗菌肽3(P3)和己基酯修饰槐糖脂(SL-HE)分别展现出作为抗菌和抗癌药物的潜力。我们团队最近的一份报告显示,将P3与SL-HE以1:8的摩尔比混合,可使肽活性提高8倍,同时SL-HE对革兰氏阳性微生物的抗菌活性提高25倍。基于这些发现,研究人员对相同的P3/SL-HE组合在两种乳腺癌细胞系上进行了评估:激素阳性细胞系BT-474和侵袭性三阴性细胞系MDA-MB-231。结果表明,P3/SL-HE的1:8摩尔比可协同增强对两种致瘤性乳腺癌细胞系的抗癌作用。机制研究表明,通过增加活性氧和线粒体功能障碍激活了内在凋亡细胞死亡机制,并通过质膜上形成孔道激活了次级程序性坏死途径。当使用成纤维细胞系CCD1065SK HDF来确定选择性时,与单独使用SL-HE相比,SL-HE/P3协同组合表现出保护特性,因此具有显著提高的选择性指数。鉴于本文报道的有前景的结果,P3/SL-HE的协同组合构成了一种值得进一步研究用于治疗乳腺癌的新策略。