Chiruvella Kishore K, Panjamurthy Kuppusamy, Choudhary Bibha, Joy Omana, Raghavan Sathees C
Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Int J Biomed Sci. 2010 Sep;6(3):182-94.
Natural products discovered from medicinal plants have played an important role in the treatment of cancer. Methyl angolensate (MA), a tetranortriterpenoid obtained from the root callus of Indian Redwood tree, Soymida febrifuga Roxb. (A.Juss) was tested for its anticancer properties on breast cancer cells.
Cell viability was tested using trypan blue, MTT and LDH assays. Tritiated thymidine assay and flowcytometry were used to study effect of MA on cell proliferation. The activation of apoptosis was checked by annexin V and JC-1 staining followed by FACS analysis. Immunoblotting analysis was used for studying expression of apoptotic and DNA double strand break repair proteins.
We find that MA inhibited the growth of breast cancer cell line, T47D in a time- and dose-dependent manner. MA treatment led to the inhibition of cell proliferation as detected by tritiated thymidine assay and flowcytometry. Further, MA treated cells exhibited typical apoptotic morphological changes and led to the accumulation of subG1 peak in cell cycle distribution. The induction of apoptosis was further confirmed both by annexin V staining and JC1 staining. We also find that MA activates MAP kinase pathway to induce apoptosis. Besides, we find a time dependent activation followed by degradation of DNA double-strand break repair proteins upon treatment with MA.
These results suggest that MA induces cytotoxicity in breast cancer cells. Further, the altered expression of DSB repair proteins in MA treated cells may control the induction of apoptosis in these cancer cells.
从药用植物中发现的天然产物在癌症治疗中发挥了重要作用。从印度红木树(Soymida febrifuga Roxb. (A.Juss))的根愈伤组织中获得的甲基安哥拉酯(MA),一种四环三萜类化合物,对其在乳腺癌细胞上的抗癌特性进行了测试。
使用台盼蓝、MTT和LDH测定法检测细胞活力。使用氚标记胸腺嘧啶核苷测定法和流式细胞术研究MA对细胞增殖的影响。通过膜联蛋白V和JC-1染色,随后进行流式细胞术分析来检查凋亡的激活情况。免疫印迹分析用于研究凋亡和DNA双链断裂修复蛋白的表达。
我们发现MA以时间和剂量依赖性方式抑制乳腺癌细胞系T47D的生长。如通过氚标记胸腺嘧啶核苷测定法和流式细胞术所检测到的,MA处理导致细胞增殖受到抑制。此外,MA处理的细胞表现出典型的凋亡形态变化,并导致细胞周期分布中亚G1峰的积累。膜联蛋白V染色和JC1染色进一步证实了凋亡的诱导。我们还发现MA激活丝裂原活化蛋白激酶途径以诱导凋亡。此外,我们发现用MA处理后,DNA双链断裂修复蛋白会出现时间依赖性的激活,随后降解。
这些结果表明MA在乳腺癌细胞中诱导细胞毒性。此外,MA处理细胞中DSB修复蛋白表达的改变可能控制这些癌细胞中凋亡的诱导。