Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
Laboratory of Natural and Synthetic Products, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
Biomed Pharmacother. 2017 Jul;91:951-963. doi: 10.1016/j.biopha.2017.05.027. Epub 2017 May 13.
Continuous increases in the rates of tumor diseases have highlighted the need for identification of novel and inexpensive antitumor agents from natural sources. In this study, we investigated the effects of enriched fraction from hydroalcoholic Brazilian red propolis extract against Hep-2 cancer cell line. Initially 201 fractions were arranged in 12 groups according to their chromatographic characteristics (A-L). After an in vitro cell viability screening, J and L were further selected as promising enriched fractions for this study. The chemical characterization was performed and Biochanin A, Formononetin, and Liquiritigenin compounds were quantified. Through MTT viability assay and morphological changes observed by Giemsa and DAPI staining, the results showed that red propolis inhibited cancer cells growth. Flow cytometry results indicated effects that were partly mediated through programmed cell death as confirmed by externalization of phosphatidylserine, DNA cleaved assay, increase at SUB G1-G0 phase in cell cycle analysis and loss of mitochondrial membrane potential. In conclusion, our results demonstrated that red propolis enriched fractions promoted apoptotic effects in human cancer cells through the mechanisms involving mitochondrial perturbation. Therefore, red propolis fractions contain candidate agents for adjuvant cancer treatment, which further studies should elucidate the comprehensive mechanistic pathways.
肿瘤疾病的发病率不断上升,这凸显了从天然来源中寻找新型、廉价抗肿瘤药物的必要性。在这项研究中,我们研究了巴西红蜂胶水醇提物富集部分对 Hep-2 癌细胞系的作用。最初,根据其色谱特征(A-L)将 201 个馏分排列成 12 组。经过体外细胞活力筛选,J 和 L 被进一步选为这项研究的有前途的富集部分。进行了化学成分鉴定,并定量了大豆苷元、芒柄花素和甘草素等化合物。通过 MTT 活力测定和吉姆萨(Giemsa)和 DAPI 染色观察到的形态变化,结果表明红蜂胶抑制了癌细胞的生长。流式细胞术结果表明,部分通过细胞程序性死亡来介导这些作用,这通过磷脂酰丝氨酸的外化、DNA 切割测定、细胞周期分析中 SUB G1-G0 期的增加以及线粒体膜电位的丧失得到证实。总之,我们的结果表明,红蜂胶富集部分通过涉及线粒体扰动的机制促进了人类癌细胞的凋亡作用。因此,红蜂胶馏分可能含有辅助癌症治疗的候选药物,进一步的研究应该阐明其全面的机制途径。