Rocha Gleice da Graça, Simões Marisol, Lúcio Kelly Araujo, Oliveira Rodrigo Rodrigues, Coelho Kaplan Maria Auxiliadora, Gattass Cerli Rocha
Lab. de Imunologia Celular, Instituto de Biofísica Carlos Chagas Filho, CCS B1 G, Universidade Federal do Rio de Janeiro, 21949-900 Rio de Janeiro, RJ, Brazil.
Bioorg Med Chem. 2007 Dec 1;15(23):7355-60. doi: 10.1016/j.bmc.2007.07.020. Epub 2007 Aug 22.
The cytotoxicity of four triterpenoids, euscaphic acid (1), tormentic acid (2), 2alpha-acetyl tormentic acid (3), and 3beta-acetyl tormentic acid (4), isolated from the roots of Cecropia lyratiloba (Moraceae) by countercurrent chromatography, was evaluated in vitro in sensitive and multidrug resistant leukemia cell lines. A structure/activity relationship analysis of the compounds was performed. Acetylation of compound 2 at C2 increased its activity by a factor of 2 while acetylation at C3 had a smaller effect. Compound 1 induces death by activation of caspase-3, dependent apoptotic pathway. Furthermore, the four triterpenoids were also active toward a multidrug resistant (MDR) leukemia cell line, overexpressing glycoprotein-P (P-gp). These results reveal the potential of the terpenoids as source for the development of new anti-neoplastic and anti-MDR drugs.
通过逆流色谱法从琴叶榕(桑科)根部分离得到的四种三萜类化合物,即悬钩子酸(1)、 tormentic酸(2)、2α-乙酰基tormentic酸(3)和3β-乙酰基tormentic酸(4),在敏感和多药耐药白血病细胞系中进行了体外细胞毒性评估。对这些化合物进行了结构/活性关系分析。化合物2在C2位乙酰化使其活性提高了2倍,而在C3位乙酰化的影响较小。化合物1通过激活caspase-3依赖的凋亡途径诱导细胞死亡。此外,这四种三萜类化合物对过表达糖蛋白P(P-gp)的多药耐药(MDR)白血病细胞系也有活性。这些结果揭示了萜类化合物作为开发新型抗肿瘤和抗多药耐药药物来源的潜力。