Chiu Sheng-Chun, Chiu Tsung-Lang, Huang Sung-Ying, Chang Shu-Fang, Chen Shee-Ping, Pang Cheng-Yoong, Hsieh Teng-Fu
Department of Research, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taichung, Taiwan.
Department of Laboratory Medicine, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taichung, Taiwan.
BMC Complement Altern Med. 2017 Dec 6;17(1):523. doi: 10.1186/s12906-017-2034-3.
N-butylidenephthalide (BP) isolated from Radix Angelica Sinensis (Danggui) exhibits anti-tumorigenic effect in various cancer cells both in vivo and in vitro. The effect of BP in bladder cancer treatment is still unclear and worth for further investigate.
Changes of patients with bladder cancer after Angelica Sinensis exposure were evaluated by analysis of Taiwan's National Health Insurance Research Database (NHIRD) database. The anti-proliferative effect of BP on human bladder cancer cells was investigated and their cell cycle profiles after BP treatment were determined by flow cytometry. BP-induced apoptosis was demonstrated by Annexin V-FITC staining and TUNEL assay, while the expressions of apoptosis-related proteins were determined by western blot. The migration inhibitory effect of BP on human bladder cancer cells were shown by trans-well and wound healing assays. Tumor model in NOD-SCID mice were induced by injection of BFTC human bladder cancer cells.
The correlation of taking Angelica sinensis and the incidence of bladder cancer in NHIRD imply that this herbal product is worth for further investigation. BP caused bladder cancer cell death in a time- and dose- dependent manner and induced apoptosis via the activation of caspase-9 and caspase-3. BP also suppressed the migration of bladder cancer cells as revealed by the trans-well and wound healing assays. Up-regulation of E-cadherin and down-regulation of N-cadherin were evidenced by real-time RT-PCR analysis after BP treatment in vitro. Besides, in combination with BP, the sensitivity of these bladder cancer cells to cisplatin increased significantly. BP also suppressed BFTC xenograft tumor growth, and caused 44.2% reduction of tumor volume after treatment for 26 days.
BP caused bladder cancer cell death through activation of mitochondria-intrinsic pathway. BP also suppressed the migration and invasion of these cells, probably by modulating EMT-related genes. Furthermore, combination therapy of BP with a lower dose of cisplatin significantly inhibited the growth of these bladder cancer cell lines. The incidence of bladder cancer decreased in patients who were exposed to Angelica sinensis, suggesting that BP could serve as a potential adjuvant in bladder cancer therapy regimen.
从当归中分离出的正丁烯基苯酞(BP)在体内和体外对多种癌细胞均具有抗肿瘤作用。BP在膀胱癌治疗中的作用仍不清楚,值得进一步研究。
通过分析台湾国民健康保险研究数据库(NHIRD)评估当归暴露后膀胱癌患者的变化。研究了BP对人膀胱癌细胞的抗增殖作用,并通过流式细胞术测定BP处理后其细胞周期谱。通过膜联蛋白V-FITC染色和TUNEL测定法证明BP诱导的细胞凋亡,同时通过蛋白质印迹法测定凋亡相关蛋白的表达。通过Transwell和伤口愈合试验显示BP对人膀胱癌细胞的迁移抑制作用。通过注射BFTC人膀胱癌细胞在NOD-SCID小鼠中诱导肿瘤模型。
NHIRD中服用当归与膀胱癌发病率的相关性表明该草药产品值得进一步研究。BP以时间和剂量依赖性方式导致膀胱癌细胞死亡,并通过激活caspase-9和caspase-3诱导细胞凋亡。如Transwell和伤口愈合试验所示,BP还抑制了膀胱癌细胞的迁移。体外BP处理后通过实时RT-PCR分析证明E-钙粘蛋白上调和N-钙粘蛋白下调。此外,与BP联合使用时,这些膀胱癌细胞对顺铂的敏感性显著增加。BP还抑制了BFTC异种移植肿瘤的生长,治疗26天后肿瘤体积减少了44.2%。
BP通过激活线粒体内在途径导致膀胱癌细胞死亡。BP还可能通过调节EMT相关基因抑制这些细胞的迁移和侵袭。此外,BP与低剂量顺铂的联合治疗显著抑制了这些膀胱癌细胞系的生长。接触当归的患者膀胱癌发病率降低,表明BP可作为膀胱癌治疗方案中的潜在佐剂。