Hazawa Masaharu, Wada Koji, Takahashi Kenji, Mori Takao, Kawahara Norio, Kashiwakura Ikuo
Department of Radiological Life Sciences, Hirosaki University Graduate School of Health Sciences, 66-1 Hon-cho, Hirosaki, 036-8564, Japan.
Invest New Drugs. 2009 Apr;27(2):111-9. doi: 10.1007/s10637-008-9141-4. Epub 2008 Jun 13.
Little information has so far been reported regarding the antiproliferative properties of Aconitum alkaloids against human tumor cells despite of their intense toxicities. In the present study, the antitumor properties and radiation sensitizing effects were investigated by various types of novel derivatives prepared from Aconitum alkaloids. The antitumor properties were investigated against human tumor cell lines, A172, A549, HeLa and Raji, respectively, by a cell growth, a clonogenic assay, cell cycle distribution, cell cycle related molecules and gammaH2AX expression. The novel compounds derived from C(20)-diterupenoid alkaloids showed a significantly suppressive effect in all cell lines. In contrast, natural C(19)-norditerpenoid alkaloids and their derivatives showed either no effect or only a slight effect. One of the compounds also showed radiosensitizing properties on A549 cells. These effects are not related to either the cell cycle distribution, the enhancement of apoptosis or the gammaH2AX expression. Novel derivatives prepared from Aconitum alkaloids, not but natural alkaloids, clearly showed anti-proliferative activity in human tumor cell lines.
尽管乌头生物碱具有很强的毒性,但迄今为止,关于其对人类肿瘤细胞的抗增殖特性的报道却很少。在本研究中,通过从乌头生物碱制备的各种新型衍生物研究了其抗肿瘤特性和辐射增敏作用。分别通过细胞生长、克隆形成试验、细胞周期分布、细胞周期相关分子和γH2AX表达,研究了对人肿瘤细胞系A172、A549、HeLa和Raji的抗肿瘤特性。源自C(20)-二萜生物碱的新型化合物在所有细胞系中均显示出显著的抑制作用。相比之下,天然C(19)-去甲二萜生物碱及其衍生物要么没有作用,要么只有轻微作用。其中一种化合物对A549细胞也显示出辐射增敏特性。这些作用与细胞周期分布、凋亡增强或γH2AX表达均无关。由乌头生物碱制备的新型衍生物,而非天然生物碱,在人肿瘤细胞系中明显显示出抗增殖活性。