Laboratory of Applied Biotechnology (LBA3B), AZM Center for Research in Biotechnology and its Applications, Doctoral School for Sciences and Technology, Lebanese University, Tripoli 1300, Lebanon.
Department of Biology and Department of Anatomy, Cell Biology and Physiological Sciences, American University of Beirut, Beirut 1107 2020, Lebanon.
Molecules. 2020 Apr 24;25(8):1993. doi: 10.3390/molecules25081993.
Brown algae are a novel resource of biogenic molecules, however few studies have been conducted in the Mediterranean to assess the cytotoxic mechanisms of algal-derived compounds. This study focuses on the antineoplastic activity of extracts from non-investigated algae of the Lebanese coast, . Extracts' antineoplastic activities were evaluated by MTT and trypan blue on different tumorigenic cells. Results indicated that the most potent extract was obtained by soxhlet using dichloromethane:methanol solvent (DM soxhlet) against HCT-116. Wound healing assay confirmed that this extract decreased the migration potential of HCT-116 cells with minimal effects on non-tumorigenic cells. It also induced an increase in the subG1 population as determined by flow cytometry. Western blot analysis demonstrated that apoptosis in treated HCT-116 cells was induced via upregulation of p21 protein and downregulation of the anti-apoptotic Bcl 2, which led to caspases activation. The latter, catalyzes the degradation of PARP-1, and thus suppresses cancer proliferation. Morphological alterations, further confirmed apoptosis. A strong pro-oxidant activity evidenced by the enhanced generation of reactive oxygen species (ROS) was observed in HCT-116 treated cells. Interestingly, a strong antioxidant effectively blocked effect induced by the extract. These results indicate that is a source of bioactive compounds possessing pro-apoptotic and anti-migratory efficacy.
褐藻是生物分子的新型资源,但在地中海地区几乎没有研究评估藻类衍生化合物的细胞毒性机制。本研究重点研究了来自黎巴嫩海岸未经研究的藻类的提取物的抗肿瘤活性。通过 MTT 和台盼蓝评估提取物的抗肿瘤活性,针对不同的肿瘤细胞。结果表明,最有效的提取物是使用二氯甲烷:甲醇溶剂(DM 索氏提取法)从. 中提取的,对 HCT-116 效果最佳。划痕愈合试验证实,该提取物可降低 HCT-116 细胞的迁移能力,对非肿瘤细胞的影响最小。通过流式细胞术检测还发现,它诱导了 subG1 群体的增加。Western blot 分析表明,在处理的 HCT-116 细胞中,通过上调 p21 蛋白和下调抗凋亡 Bcl-2 诱导细胞凋亡,从而激活半胱天冬酶。后者催化 PARP-1 的降解,从而抑制癌症增殖。形态学改变进一步证实了细胞凋亡。在 HCT-116 处理的细胞中观察到活性氧(ROS)生成增强,证明具有很强的促氧化活性。有趣的是,一种强烈的抗氧化剂可有效阻断提取物的作用。这些结果表明, 是具有促凋亡和抗迁移作用的生物活性化合物的来源。