Zhang Jinghui, Hong Yanjun, Xie Peisi, Chen Yang, Jiang Lilong, Yang Zhiyi, Cao Guodong, Chen Zhongjian, Liu Xuesong, Chen Yong, Wu Yongjiang, Cai Zongwei
College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
Department of Chemistry, State Key Laboratory of Environmental and Biological Analysis, Hong Kong Baptist University, Hong Kong, China.
Front Pharmacol. 2021 Jan 12;11:593815. doi: 10.3389/fphar.2020.593815. eCollection 2020.
Bufalin (BFL) and cinobufagin (CBF) are the principal bioactive constituents of Chansu, a widely used traditional Chinese medicine (TCM). The synergistic effects of potential active components are responsible for the bioactivities of TCM. Our results showed that the cotreatment with BFL and CBF confers superior anticancer efficacy compared to monotreatment. To reveal the underlying mechanisms of their cotreatment, an integrated method composed of mass spectrometry-based lipidomics and matrix-assisted laser desorption/ionization mass spectrometry imaging was used to delineate the responses of tumor-bearing mice treated with BFL and CBF individually or in combination. The cotreatment with BFL and CBF modulated the sphingolipid metabolism and glycerophospholipid metabolism, and subsequently led to mitochondria-driven apoptosis and systemic disruption of biomembranes in tumor cells. Furthermore, we found that the disturbed lipid markers were mainly located in the non-necrotic tumor areas, the essential parts for the formation of solid tumor framework. Together, our findings revealed what occurred in tumor in response to the treatment of BFL and CBF, from lipids to enzymes, and thus provide insights into the critical role of lipid reprogramming in the satisfactory anticancer effect of BFL in combination with CBF.
蟾毒灵(BFL)和华蟾毒精(CBF)是蟾酥的主要生物活性成分,蟾酥是一种广泛使用的传统中药(TCM)。潜在活性成分的协同作用决定了中药的生物活性。我们的结果表明,与单独用药相比,BFL和CBF联合用药具有更强的抗癌效果。为了揭示其联合用药的潜在机制,我们采用了一种由基于质谱的脂质组学和基质辅助激光解吸/电离质谱成像组成的综合方法,来描绘单独或联合使用BFL和CBF治疗的荷瘤小鼠的反应。BFL和CBF联合用药调节了鞘脂代谢和甘油磷脂代谢,随后导致肿瘤细胞中线粒体驱动的凋亡和生物膜的系统性破坏。此外,我们发现受干扰的脂质标志物主要位于非坏死肿瘤区域,这些区域是实体瘤框架形成的关键部分。总之,我们的研究结果揭示了肿瘤对BFL和CBF治疗的反应,从脂质到酶,从而为脂质重编程在BFL与CBF联合使用的满意抗癌效果中的关键作用提供了见解。