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糙皮齿菌中齿菌酸G对HeLa细胞的抗增殖和诱导凋亡活性。

Anti-proliferative and apoptosis-inducible activity of Sarcodonin G from Sarcodon scabrosus in HeLa cells.

作者信息

Dong Mei, Chen Shi-Ping, Kita Kazuko, Ichimura Yoshinobu, Guo Wen-Zhi, Lu Sa, Sugaya Shigeru, Hiwasa Takaki, Takiguchi Masaki, Mori Naomi, Kashima Atsushi, Morimura Keiji, Hirota Mitsuru, Suzuki Nobuo

机构信息

Department of Medicinal Natural Product Chemistry, School of Pharmaceutical Sciences, Hebei Medical University, Shijiazhuang 050017, P.R. China.

出版信息

Int J Oncol. 2009 Jan;34(1):201-7.

Abstract

There is an ongoing search for plant-derived diterpenes, especially for diterpenes with anti-inflammatory activity that also have anti-proliferative effects on human cancer cells. A cyathane-type diterpene, Sarcodonin G (SG), isolated from the mushroom Sarcodon scabrosus and already reported to have anti-inflammatory activity, inhibited proliferation of HeLa cells to the greatest extent among 4 cyathane diterpenes tested. SG showed an IC50 (50% inhibition concentration) of 20 microM, estimated by MTT assay 2 days after culture of cells with the chemical. SG treatment of HeLa cells resulted in dose-dependent generation of apoptotic events such as DNA-laddering (< or =100 microM). Moreover, SG-treated HeLa cells showed activation of caspase-3 and caspase-9 and increase of Bax/Bcl-2 ratios, as analyzed by Western blot analysis. The anti-proliferative effects of SG treatment on HeLa cells were lessened by a caspase inhibitor, Z-VAD-FMK. SG also showed anti-proliferative effects toward 5 other human cancer cell lines with IC50 values of 20-40 microM. Because of these anti-proliferative effects via possible caspase activation, SG holds promise of being a novel anti-proliferative agent deserving further investigation.

摘要

人们一直在寻找植物来源的二萜类化合物,尤其是具有抗炎活性且对人类癌细胞具有抗增殖作用的二萜类化合物。从糙皮齿菌中分离出的一种杯伞烷型二萜类化合物,齿孔酸G(SG),已报道具有抗炎活性,在测试的4种杯伞烷二萜类化合物中,它对HeLa细胞增殖的抑制作用最大。通过MTT法在细胞与该化合物培养2天后估计,SG的IC50(50%抑制浓度)为20微摩尔。用SG处理HeLa细胞导致剂量依赖性的凋亡事件发生,如DNA梯状条带(≤100微摩尔)。此外,通过蛋白质印迹分析,经SG处理的HeLa细胞显示出caspase-3和caspase-9的激活以及Bax/Bcl-2比值的增加。caspase抑制剂Z-VAD-FMK减弱了SG处理对HeLa细胞的抗增殖作用。SG对其他5种人类癌细胞系也显示出抗增殖作用,IC50值为20 - 40微摩尔。由于通过可能的caspase激活产生的这些抗增殖作用,SG有望成为一种值得进一步研究的新型抗增殖剂。

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