Institute for Clinical & Experimental Surgery, University of Saarland, 66421 Homburg/Saar, Germany.
Institute for Clinical & Experimental Surgery, University of Saarland, 66421 Homburg/Saar, Germany.
Life Sci. 2013 Jul 19;93(1):44-50. doi: 10.1016/j.lfs.2013.05.022. Epub 2013 Jun 3.
The herbal compound 4-hydroxybenzyl alcohol (HBA) is a pleiotropic agent, which has been shown to effectively inhibit the development of new blood vessels by targeting multiple mechanisms of the angiogenic process. Because angiogenesis is a major prerequisite for tumor growth, the aim of this study was to analyze for the first time, whether HBA may be used for anti-cancer therapy.
CT26.WT colon carcinoma cells were exposed to different HBA doses to study their viability, migration, invasiveness and protein expression compared to vehicle-treated controls. Moreover, CT26.WT cell spheroids were transplanted into the dorsal skinfold chamber of HBA-treated and vehicle-treated BALB/c mice for the analysis of tumor vascularization and growth by means of repetitive intravital fluorescence microscopy, histology and immunohistochemistry.
As shown by water-soluble tetrazolium (WST)-1 and lactate dehydrogenase (LDH) assays, HBA treatment dose-dependently reduced the viability and integrity of the tumor cells. Moreover, phalloidin staining of HBA-treated cells revealed a disorganized cytoskeleton, which was associated with a decreased cellular migratory and invasive activity. In addition, the cells presented with a significantly increased expression of the apoptosis marker cleaved caspase-3 and a decreased expression of vascular endothelial growth factor (VEGF) and matrix metalloproteinase (MMP)-9 when compared to controls. Finally, HBA treatment inhibited the vascularization and growth of newly developing CT26.WT tumors in the mouse dorsal skinfold chamber model without affecting the normal behavior of the animals.
These novel findings indicate that HBA represents a promising candidate for the establishment of anti-angiogenic treatment strategies in cancer therapy.
草药化合物 4-羟基苯甲醇(HBA)是一种多效因子,已被证明通过靶向血管生成过程的多种机制有效抑制新血管的形成。由于血管生成是肿瘤生长的主要前提,本研究旨在首次分析 HBA 是否可用于癌症治疗。
将 CT26.WT 结肠癌细胞暴露于不同剂量的 HBA 下,与未经药物处理的对照组相比,研究其活力、迁移、侵袭和蛋白表达情况。此外,将 CT26.WT 细胞球移植到 HBA 处理和未经药物处理的 BALB/c 小鼠的背部皮肤囊腔中,通过重复活体荧光显微镜、组织学和免疫组织化学分析肿瘤血管生成和生长情况。
如水溶性四唑盐(WST)-1 和乳酸脱氢酶(LDH)测定所示,HBA 处理剂量依赖性地降低了肿瘤细胞的活力和完整性。此外,HBA 处理的细胞中的鬼笔环肽染色显示细胞骨架紊乱,与细胞迁移和侵袭活性降低有关。此外,与对照组相比,这些细胞Cleaved caspase-3 的凋亡标志物表达显著增加,血管内皮生长因子(VEGF)和基质金属蛋白酶(MMP)-9 的表达降低。最后,HBA 处理抑制了新形成的 CT26.WT 肿瘤在小鼠背部皮肤囊腔模型中的血管生成和生长,而不影响动物的正常行为。
这些新发现表明,HBA 是癌症治疗中建立抗血管生成治疗策略的有前途的候选药物。