Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria.
Department of Pharmacology and Toxicology, University of Vienna, Althanstr. 14, 1090 Vienna, Austria.
Toxins (Basel). 2017 Aug 24;9(9):258. doi: 10.3390/toxins9090258.
Recently, in vitro anti-cancer properties of beauvericin, a fungal metabolite were shown in various cancer cell lines. In this study, we assessed the specificity of this effect by comparing beauvericin cytotoxicity in malignant versus non-malignant cells. Moreover, we tested in vivo anticancer effects of beauvericin by treating BALB/c and CB-17/SCID mice bearing murine CT-26 or human KB-3-1-grafted tumors, respectively. Tumor size and weight were measured and histological sections were evaluated by Ki-67 and H/E staining as well as TdT-mediated-dUTP-nick-end (TUNEL) labeling. Beauvericin levels were determined in various tissues and body fluids by LC-MS/MS. In addition to a more pronounced activity against malignant cells, we detected decreased tumor volumes and weights in beauvericin-treated mice compared to controls in both the allo- and the xenograft model without any adverse effects. No significant differences were detected concerning percentages of proliferating and mitotic cells in tumor sections from treated and untreated mice. However, a significant increase of necrotic areas within whole tumor sections of beauvericin-treated mice was found in both models corresponding to an enhanced number of TUNEL-positive, i.e., apoptotic, cells. Furthermore, moderate beauvericin accumulation was detected in tumor tissues. In conclusion, we suggest beauvericin as a promising novel natural compound for anticancer therapy.
最近,真菌代谢产物伏马菌素在各种癌细胞系中的体外抗癌特性已被证明。在这项研究中,我们通过比较伏马菌素对恶性细胞和非恶性细胞的细胞毒性,来评估这种作用的特异性。此外,我们通过分别用携带鼠 CT-26 或人 KB-3-1 移植瘤的 BALB/c 和 CB-17/SCID 小鼠来治疗,检测伏马菌素的体内抗癌作用。通过测量肿瘤大小和重量,以及通过 Ki-67 和 H/E 染色以及 TdT 介导的 dUTP-尼克末端(TUNEL)标记评估组织学切片。通过 LC-MS/MS 在各种组织和体液中测定伏马菌素水平。除了对恶性细胞的活性更强外,与对照组相比,在同种异体和异种移植模型中,用伏马菌素治疗的小鼠的肿瘤体积和重量均减小,而没有任何不良反应。在来自治疗和未治疗小鼠的肿瘤切片中,增殖和有丝分裂细胞的百分比没有检测到显著差异。然而,在两种模型中均发现整个肿瘤切片中的坏死区域显著增加,这对应于 TUNEL 阳性(即凋亡)细胞数量的增加。此外,在肿瘤组织中检测到适度的伏马菌素积累。总之,我们认为伏马菌素是一种很有前途的新型天然化合物,可用于抗癌治疗。