Antitumor effects of two novel naturally occurring terpene quinones isolated from the Mediterranean ascidian Aplidium conicum

被引:48
作者
Aiello, A
Fattorusso, E
Luciano, P
Macho, A
Menna, M
Muñoz, E
机构
[1] Univ Naples Federico II, Dipartimento Chim Sostanze Nat, I-80131 Naples, Italy
[2] Univ Cordoba, Dept Biol Celular Fisiol & Immunol, E-14004 Cordoba, Spain
关键词
D O I
10.1021/jm0489915
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The ascidian Aphdium conicum collected along Sardinia coasts (Italy) contained two novel prenylated benzoquinones, designated thiaplidiaquinone A (1) and thiaplidiaquinone B (2). These compounds showed an unprecedented tetracyclic structure. We have studied the proapototic mechanisms of both prenylated benzoquinones in the Jurkat cell line that is derived from a human T lymphoma, and we show that both compounds induce a strong production of intracellular reactive oxygen species (ROS) in this cell line. Moreover, kinetic experiments, comparing the timing of ROS induction with the collapse of the mitochondria potential (Delta Psi(m)), clearly showed that ROS preceded the disruption of the mitochondrial potential, and the later one paralleled the appearance of apoptotic cells. Thus, thiaplidiaquinones A and B can enter into the cells and induce cell death by apoptosis.
引用
收藏
页码:3410 / 3416
页数:7
相关论文
共 32 条
[1]   Conicaquinones A and B, two novel cytotoxic terpene quinones from the Mediterranean ascidian Aplidium conicum [J].
Aiello, A ;
Fattorusso, E ;
Luciano, P ;
Menna, M ;
Esposito, G ;
Iuvone, T ;
Pala, D .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2003, 2003 (05) :898-900
[2]   PROTEIN-TYROSINE KINASE INHIBITORY PROPERTIES OF PLANAR POLYCYCLICS OBTAINED FROM THE MARINE SPONGE XESTOSPONGIA CF CARBONARIA AND FROM TOTAL SYNTHESIS [J].
ALVI, KA ;
RODRIGUEZ, J ;
DIAZ, MC ;
MORETTI, R ;
WILHELM, RS ;
LEE, RH ;
SLATE, DL ;
CREWS, P .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (18) :4871-4880
[3]  
BENCHEKROUN MN, 1994, FREE RADICAL BIO MED, V17, P191
[4]   Modulation of the mitochondrial permeability transition pore by pyridine nucleotides and dithiol oxidation at two separate sites [J].
Costantini, P ;
Chernyak, BV ;
Petronilli, V ;
Bernardi, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (12) :6746-6751
[5]   Longithorones J and K, two new cyclofarnesylated quinone derived metabolites from the Australian ascidian Aplidium longithorax [J].
Davis, RA ;
Carroll, AR ;
Quinn, RJ .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (01) :158-160
[6]   Longithorols C-E.: Three new macrocyclic sesquiterpene hydroquinone metabolites from the Australian ascidian, Aplidium longithorax [J].
Davis, RA ;
Carroll, AR ;
Quinn, RJ .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (10) :1405-1409
[7]  
DETINGUYMOREAUD E, 1994, ANTICANCER RES, V14, P99
[8]   Marine natural products [J].
Faulkner, DJ .
NATURAL PRODUCT REPORTS, 2002, 19 (01) :1-48
[9]  
Fenical W., 1976, FOOD DRUGS SEA P, V4, P388
[10]   Longithorols A and B, novel prenylated paracyclophane- and metacyclophane-type hydroquinones from the tunicate Aplidium longithorax [J].
Fu, X ;
Ferreira, MLG ;
Schmitz, FJ .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (09) :1306-1310