Dinnen R D, Ebisuzaki K
Department of Microbiology and Immunology, University of Western Ontario, London, Canada.
Anticancer Res. 1997 Mar-Apr;17(2A):1027-33.
One alternative approach to the current use of cytotoxic anticancer drugs involves the use of differentiation-inducing agents. However, a wider application of this strategy would require the development of assays to search for new differentiation-inducing agents. In this report we describe an in vitro assay using the murine erythroleukemia (clone 3-1) cells. Tests for the efficacy of this assay for the analysis of antineoplastic activity in natural products led to studies on pau d'arco, a South American folklore product used in the treatment of cancer. Purification of the activity in aqueous extracts by solvent partition and thin layer chromatography (TLC) indicated the presence of two activities, one of which was identified as lapachol. The activity in the pau d'arco extracts and of lapachol was inhibited by vitamin K1. As a vitamin K antagonist, lapachol might target such vitamin K-dependent reactions as the activation of a ligand for the Axl receptor tyrosine kinase.
一种替代当前使用细胞毒性抗癌药物的方法是使用分化诱导剂。然而,要更广泛地应用这一策略,就需要开发用于寻找新的分化诱导剂的检测方法。在本报告中,我们描述了一种使用小鼠红白血病(克隆3-1)细胞的体外检测方法。对该检测方法分析天然产物抗肿瘤活性的功效进行的测试,引发了对伯尔卫木的研究,伯尔卫木是一种用于治疗癌症的南美民间药物。通过溶剂分配和薄层色谱法(TLC)对水提取物中的活性进行纯化,结果表明存在两种活性,其中一种被鉴定为拉帕醇。伯尔卫木提取物和拉帕醇中的活性受到维生素K1的抑制。作为一种维生素K拮抗剂,拉帕醇可能靶向诸如激活Axl受体酪氨酸激酶配体等维生素K依赖性反应。