Dai Zhi, Li Shi-Rong, Zhu Pei-Feng, Liu Lu, Wang Bei, Liu Ya-Ping, Luo Xiao-Dong, Zhao Xu-Dong
Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences/Key Laboratory of Bioactive Peptides of Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China; Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming, Yunnan 650204, China.
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China; Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming, Yunnan 650204, China.
Bioorg Med Chem Lett. 2017 Jul 1;27(13):2863-2867. doi: 10.1016/j.bmcl.2017.04.075. Epub 2017 Apr 26.
Glioblastoma multiform (GBM) is a highly aggressive brain tumor with poor life expectancy, and glioma stem cells (GSCs) are a small population of tumor cells existed in GBM, in which GSCs response to drive GBM recurrence, invasion and contribute to the anti-cancer resistance. GSCs have been identified and developed as a therapeutic target for GBM and can be used in drugs screening. Isocostunolide is a natural sesquiterpenoid and contained abundant resource in medicinal plants, but the anti-cancer efficacies of it against GSCs are still unexplored. In this investigation, the anti-tumor activity of isocostunolide against GSCs was investigated and the result demonstrated that it inhibited the growth of GSCs (GSC-3#, GSC-12#, GSC-18#) significantly with an IC value of 2.80μg/ml, 2.61μg/ml, 1.07μg/ml, respectively. In further mechanism study, isocostunolide inhibited GSCs cell proliferation, induced GSCs apoptosis significantly, as well as increased the proportion of the cleavage of caspase-3. The result suggested that isocostunolide induced GSCs apoptosis via the caspase dependent apoptotic pathway. Moreover, isocostunolide damaged GSCs colony formation capacity significantly and exhibited the anti-cancer efficacy against GSCs in vitro.
多形性胶质母细胞瘤(GBM)是一种侵袭性很强的脑肿瘤,患者预期寿命较短,而胶质瘤干细胞(GSCs)是存在于GBM中的一小部分肿瘤细胞,其中GSCs会促使GBM复发、侵袭并导致抗癌耐药性。GSCs已被确定并开发为GBM的治疗靶点,可用于药物筛选。异土木香内酯是一种天然倍半萜类化合物,在药用植物中资源丰富,但其对GSCs的抗癌效果仍未得到探索。在本研究中,研究了异土木香内酯对GSCs的抗肿瘤活性,结果表明它能显著抑制GSCs(GSC-3#、GSC-12#、GSC-18#)的生长,IC值分别为2.80μg/ml、2.61μg/ml、1.07μg/ml。在进一步的机制研究中,异土木香内酯抑制GSCs细胞增殖,显著诱导GSCs凋亡,并增加caspase-3裂解的比例。结果表明,异土木香内酯通过caspase依赖性凋亡途径诱导GSCs凋亡。此外,异土木香内酯显著破坏GSCs的集落形成能力,并在体外表现出对GSCs的抗癌效果。