Geeraerts B, Vanhoecke B, Vanden Berghe W, Philippé J, Offner F, Deforce D
Laboratory of Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.
Leukemia. 2007 Aug;21(8):1610-8. doi: 10.1038/sj.leu.2404788. Epub 2007 Jun 14.
We investigated if deguelin, a naturally occurring rotenoid, was able to inhibit nuclear factor kappa B (NF-kappaB)-binding protein (IkappaBalpha) expression and to induce apoptosis in B-cell chronic lymphocytic leukemia (B-CLL) cells in vitro. Deguelin-induced cell death in the majority of B-CLL cells and was found to be more toxic toward B-CLL cells than to the normal mononuclear or B-cells, suggesting selectivity towards the malignant cells. Deguelin was found to reduce IkappaBalpha protein expression, and thus interacts with the NFkappaB pathway. The induced apoptosis was characterized by processing of caspase-9 and -3 and poly-(ADP)-ribose-polymerase cleavage. Exposure of B-CLL cells to deguelin resulted in Bcl2-associated protein (Bax) conformational changes and downregulation of the key survival protein myeloid cell leukemia sequence 1 (Mcl-1), which is associated with response to treatment in B-CLL patients. Deguelin retained its ability to induce apoptosis in B-CLL cells in the presence of interleukin-4, a pro-survival cytokine in B-CLL, and when cultured with 50% human serum. These data indicate that deguelin is able to induce apoptosis in B-CLL cells in the presence of pro-survival signals and thus merits further investigation for clinical application either as a single agent or in combination with other anticancer agents.
我们研究了鱼藤素(一种天然存在的鱼藤酮类化合物)是否能够抑制核因子κB(NF-κB)结合蛋白(IκBα)的表达,并在体外诱导B细胞慢性淋巴细胞白血病(B-CLL)细胞凋亡。鱼藤素可诱导大多数B-CLL细胞死亡,并且发现其对B-CLL细胞的毒性比对正常单核细胞或B细胞更大,表明对恶性细胞具有选择性。研究发现鱼藤素可降低IκBα蛋白表达,从而与NFκB信号通路相互作用。诱导的凋亡表现为半胱天冬酶-9和-3的激活以及聚(ADP)核糖聚合酶的裂解。将B-CLL细胞暴露于鱼藤素会导致Bcl2相关蛋白(Bax)构象改变以及关键存活蛋白髓系细胞白血病序列1(Mcl-1)的下调,而Mcl-1与B-CLL患者的治疗反应相关。在白细胞介素-4(B-CLL中的一种促存活细胞因子)存在的情况下以及与50%人血清一起培养时,鱼藤素仍保留其诱导B-CLL细胞凋亡的能力。这些数据表明,鱼藤素在存在促存活信号的情况下能够诱导B-CLL细胞凋亡,因此作为单一药物或与其他抗癌药物联合使用在临床应用方面值得进一步研究。