Wang Dongdong, Jiang Yun, Wu Ke, Wang Shu, Wang Yitao
Department of Pharmacognosy, West China College of Pharmacy, Sichuan University, No. 17, Duan 3, Renmin Nan Road, Chengdu, 610041, Peoples' Republic of China.
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Science, University of Macau, Macau, 999078, Peoples' Republic of China.
BMC Complement Altern Med. 2015 Feb 21;15:29. doi: 10.1186/s12906-015-0551-5.
Cancer is well known as a leading cause of death in the world. At present, it is the very active area to search for anticancer drugs from natural products. In this study, we evaluated the antitumor property of chloroform extract (CE), n-hexane extract (HE), water extract (WE) and steroidal alkaloids from the cultivated Bulbus Fritillariae ussuriensis (BFU) and its preliminary mechanism for its action was investigated.
Firstly, cytotoxicity of the different extracts from BFU against Lewis lung carcinoma cell line (LLC), Human ovarian cancer cell line (A2780), human hepatocellular carcinoma cell line (HepG2), human lung carcinoma cell line (A549) was measured by MTT assay. Then, we identified the compounds from the active extract of BFU by bioassay guided isolation, determined their antitumor activity in vitro, and detected cell cycle distribution using flow cytometry. Moreover, the extract of BFU which showed remarked anti-proliferative activity in vitro was further evaluated using S180 and LLC tumor models. Additionally, a preliminary investigation of the mechanism of the action was carried out by using histological and immunohistochemical staining technique.
The results showed that CE and the purified total alkaloids of BFU (TAFU) exhibited stronger cytotoxic activity than the others (WE and HE). We further isolated the four main steroidal alkaloids from TAFU, and found all alkaloids showed significant cytotoxicity, and peimisine induced G0/G1 phase arrest and increased apoptosis. The results showed that TAFU had significant antitumor activity and low toxicity in vivo. Additionally, the immunohistochemical examinations signified that TAFU remarkably increased caspase-3 expression and reduced microvessel density (MVD) in tumor tissues of transplantable S180 and LLC tumor models.
These results achieved suggested that the steroidal alkaloids could hold a good potential for use as an antitumor drug. Notably, our finding is the first report on the antitumor activity of extracts and steroidal alkaloids from the cultivated BFU in vitro and in vivo and its mechanisms.
癌症是全球主要的死亡原因之一。目前,从天然产物中寻找抗癌药物是一个非常活跃的领域。在本研究中,我们评估了栽培的川贝母氯仿提取物(CE)、正己烷提取物(HE)、水提取物(WE)和甾体生物碱的抗肿瘤特性,并研究了其作用的初步机制。
首先,采用MTT法测定川贝母不同提取物对Lewis肺癌细胞系(LLC)、人卵巢癌细胞系(A2780)、人肝癌细胞系(HepG2)、人肺癌细胞系(A549)的细胞毒性。然后,通过生物活性导向分离鉴定川贝母活性提取物中的化合物,测定其体外抗肿瘤活性,并使用流式细胞术检测细胞周期分布。此外,使用S180和LLC肿瘤模型进一步评估在体外显示出显著抗增殖活性的川贝母提取物。另外,采用组织学和免疫组织化学染色技术对作用机制进行初步研究。
结果表明,CE和川贝母纯化总生物碱(TAFU)表现出比其他提取物(WE和HE)更强的细胞毒性活性。我们进一步从TAFU中分离出四种主要甾体生物碱,发现所有生物碱均表现出显著的细胞毒性,且浙贝母碱诱导G0/G1期阻滞并增加细胞凋亡。结果表明,TAFU在体内具有显著的抗肿瘤活性且毒性较低。此外,免疫组织化学检查表明,TAFU显著增加可移植S180和LLC肿瘤模型肿瘤组织中caspase-3的表达并降低微血管密度(MVD)。
这些结果表明甾体生物碱具有作为抗肿瘤药物的良好潜力。值得注意的是,我们的发现是关于栽培川贝母提取物和甾体生物碱体外和体内抗肿瘤活性及其机制的首次报道。