Antiproliferative activity and apoptosis induction by trijuganone C isolated from the root of Salvia miltiorrhiza Bunge (Danshen)

被引:20
|
作者
Uto, Takuhiro [1 ]
Nguyen Huu Tung [1 ,2 ]
Ohta, Tomoe [1 ]
Juengsanguanpornsuk, Wipawee [1 ,3 ]
Le Quoc Hung [2 ]
Nguyen Thanh Hai [2 ]
Dinh Doan Long [2 ]
Phuong Thien Thuong [2 ,4 ]
Okubo, Shinya [1 ]
Hirata, Sakiko [1 ]
Shoyama, Yukihiro [1 ]
机构
[1] Nagasaki Int Univ, Fac Pharmaceut Sci, Dept Pharmacognosy, 2825-7 Huis Ten Bosch, Sasebo, Nagasaki 8593298, Japan
[2] Vietnam Natl Univ, Sch Med & Pharm, Hanoi, Vietnam
[3] Khon Kaen Univ, Fac Pharmaceut Sci, Khon Kaen 40002, Thailand
[4] Natl Inst Med Mat, 3B Quang Trung St, Hanoi, Vietnam
关键词
antiproliferation; apoptosis; Danshen; leukemia cells; Salvia miltiorrhiza; trijuganone C; TANSHINONE IIA DERIVATIVES; LEUKEMIA-CELL LINES; VASODILATIVE ACTIVITY; BCL-2; FAMILY; CANCER; THERAPEUTICS; CONSTITUENTS; TRITERPENES; JAPONICA; DEATH;
D O I
10.1002/ptr.6013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, we found that the hexane fraction of Danshen, the dried root of Salvia miltiorrhiza (Lamiaceae), exerted antiproliferative effects on human leukemia cells. Phytochemical investigation of the hexane fraction achieved the isolation of the tanshinone diterpenes: dihydrotanshinone I (1), trijuganone C (2), trijuganone B (3), cryptotanshinone (4), tanshinone IIA (5), and tanshinone I (6). Compound 2 showed significant antiproliferative activities against human leukemia cells HL-60, Jurkat, and U937. The antiproliferative activities of 2 against human cancer and normal cells indicated that 2 exhibited potent antiproliferative activities with IC50 values less than 10M against HL-60 and Jurkat cells as well as on the colon cancer cells DLD-1, COLO 205, and Caco-2. Compound 2 induced chromatin condensation, DNA fragmentation, activation of caspase-3, -8, and -9, and the cleavage of poly (ADP-ribose) polymerase (PARP) in HL-60 cells. Moreover, 2 activated Bid and Bax, leading to the loss of mitochondrial membrane potential, and 2 induced the cytochrome c release from mitochondria into cytosol. In contrast, Bcl-2 and Bcl-xL were unaffected by 2. These results suggest that 2 exerts antiproliferative effects via apoptosis induction mediated by mitochondrial dysfunction and caspase activation. Compound 2 may serve as a candidate of potential chemotherapeutic agent for human leukemia.
引用
收藏
页码:657 / 666
页数:10
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