Novel drug amooranin induces apoptosis through caspase activity in human breast carcinoma cell lines

被引:36
作者
Rabi, T
Ramachandran, C
Fonseca, HB
Nair, RPK
Alamo, A
Melnick, SJ
Escalon, E
机构
[1] Miami Childrens Hosp, Res Inst, Miami, FL 33155 USA
[2] Miami Childrens Hosp, Div Pathol, Miami, FL 33155 USA
[3] Miami Childrens Hosp, Div Hematol Oncol, Miami, FL 33155 USA
关键词
amooranin; apoptosis; breast carcinoma cells; breast epithelial cells;
D O I
10.1023/A:1024911925623
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Amooranin (AMR) is a triterpene acid isolated from the stem bark of a tropical tree (Amoora rohituka) grown wild in India. A. rohituka stem bark is one of the components of a medicinal preparation used in the Indian Ayurvedic system of medicine for the treatment of human malignancies. We investigated the mechanism of cell death associated with AMR cytotoxicity in human mammary carcinoma MCF-7, multidrug resistant breast carcinoma MCF-7/TH and breast epithelial MCF-10A cell lines. AMR IC50 values ranged between 3.8 - 6.9 mug/ml among MCF-7, MCF-7/TH and MCF-10A cells. AMR induced oligonucleosome- sized DNA ladder formation characteristic of apoptosis when tumor cells were treated with 1 - 8 mug/ml AMR for 48 h. In situ cell death detection assay indicated that AMR caused 37.3 - 72.1% apoptotic cells in MCF- 7, 32 - 48.7% in MCF- 7/TH and 0 - 37.1% in MCF- 10A cells at 1 - 8 mug/ml concentrations. The induction of apoptosis in AMR treated cells was accompanied by the elevation of total caspase and caspase-8 activities. Flow cytometric analysis showed that AMR induced caspase-8 activation in 40.8 - 71% MCF- 7, 28.5 - 43.2% MCF- 7/TH and 4 - 32.8% MCF- 10A cells at 1 - 8 mug/ml concentrations. Our results suggest that AMR is a novel drug having potential for clinical development against human malignancies.
引用
收藏
页码:321 / 330
页数:10
相关论文
共 44 条
[1]   Activation of caspases measured in situ by binding of fluorochrome-labeled inhibitors of caspases (FLICA):: Correlation with DNA fragmentation [J].
Bedner, E ;
Smolewski, P ;
Amstad, P ;
Darzynkiewicz, Z .
EXPERIMENTAL CELL RESEARCH, 2000, 259 (01) :308-313
[2]   Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death [J].
Boldin, MP ;
Goncharov, TM ;
Goltsev, YV ;
Wallach, D .
CELL, 1996, 85 (06) :803-815
[3]   Biochemical pathways of caspase activation during apoptosis [J].
Budihardjo, I ;
Oliver, H ;
Lutter, M ;
Luo, X ;
Wang, XD .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :269-290
[4]  
CARCIACALVO M, 1998, J BIOL CHEM, V273, P32608
[5]  
CHEN G, 1993, CANCER RES, V53, P2544
[6]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[7]  
COHEN JJ, 1984, J IMMUNOL, V132, P38
[8]  
CRAGG GM, 1993, ACS SYM SER, V534, P149
[9]   Mammalian caspases: Structure, activation, substrates, and functions during apoptosis [J].
Earnshaw, WC ;
Martins, LM ;
Kaufmann, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :383-424
[10]   In vitro activation of CPP32 and Mch3 by Mch4, a novel human apoptotic cysteine protease containing two FADD-like domains [J].
FernandesAlnemri, T ;
Armstrong, RC ;
Krebs, J ;
Srinivasula, SM ;
Wang, L ;
Bullrich, F ;
Fritz, LC ;
Trapani, JA ;
Tomaselli, KJ ;
Litwack, G ;
Alnemri, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7464-7469