六种三环基酸复合物的合成和抗癌活性
Zhiyu Pan1, Wen Zhong1, Yanping Li1
1Guangxi International Zhuang Medicine Hospital, Nanning 530201, China; Guangxi International Zhuang Medicine Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning 530201, China; Guangxi Institute of Ethnic Medicine, Nanning 530201, China.
Journal of inorganic biochemistry
|July 13, 2025
概括
新的C2锡复合物通过诱导细胞亡和细胞循环停止,有效地抑制HepG2肝癌细胞. 这种化合物通过DNA间隔和线粒体通路中断显示出有前途的抗癌活性.
科学领域:
- 有机金属化学 有机金属化学
- 癌症生物学 癌症生物学
- 结构化学 结构化学
背景情况:
- 三环基锡胺是一种有机金属化合物的类.
- 研究用于癌症治疗的新型化合物至关重要.
研究的目的:
- 为了合成和描述新型的三环基锡酸盐复合物.
- 为了评估这些复合物的体外抗癌活性与人类癌症细胞系.
- 为了阐明最强大的复合物的作用机制.
主要方法:
- 六种三环基锡酸盐复合物 (C1C6) 的合成和表征.
- 对C1,C2,C4和C5.5的晶体结构的确定.
- 在体外细胞毒性测定对A549,HepG2和MDA-MB-231细胞系.
- 线粒体膜潜能测定,细胞周期分析,DNA结合研究 (UV-Vis,光竞争) 和分子对接.
主要成果:
- 六个三环基锡酸盐复合物成功合成和表征.
- 综合体C1,C2和C5展示了一维链结构.
- C2复合体对HepG2细胞表现出显著的抑制活性 (IC50 = 1.31 ± 0.47 μM).
- C2通过线粒体路径诱导亡,导致G2细胞循环停止,并插入DNA.
结论:
- 该C2复合体对HepG2细胞表现出强大的抗癌活性.
- 该机制涉及线粒体亡诱导,细胞循环停止和DNA间隙.
- 三环基锡胺代表了一类有前途的抗癌药物.
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