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辛伐他汀依赖的霍奇金淋巴瘤细胞凋亡及人霍奇金肿瘤在体内的生长抑制

Simvastatin-dependent apoptosis in Hodgkin's lymphoma cells and growth impairment of human Hodgkin's tumors in vivo.

作者信息

von Tresckow Bastian, von Strandmann Elke Pogge, Sasse Stephanie, Tawadros Samir, Engert Andreas, Hansen Hinrich P

机构信息

Laboratory of Immunotherapy, Clinic I of Internal Medicine, University Hospital Cologne, Cologne, Germany.

出版信息

Haematologica. 2007 May;92(5):682-5. doi: 10.3324/haematol.11020.

Abstract

Statins are used to treat hypercholesterolemia and seem to have a preventive effect against cancer through pleiotropic effects including prenylation-inhibition. So far nothing is known about the activity of statins or more specific prenylation-inhibitors in Hodgkin's lymphoma (HL). We, therefore, evaluated the anti-HL activity of simvastatin and specific prenylation-inhibitors. 2 microM Simvastatin induced caspase-related apoptosis via depletion of prenylation-substrates in several HL-cell lines. Furthermore, it effectively impaired tumor growth in a mouse model for HL. Since the prenylation-inhibitors FTI-277 and GGTI-298 were also effective against HL-cells, we conclude that statins and specific prenylation-inhibitors should be evaluated in HL patients.

摘要

他汀类药物用于治疗高胆固醇血症,并且似乎通过包括异戊二烯化抑制在内的多效性作用对癌症具有预防作用。到目前为止,关于他汀类药物或更具特异性的异戊二烯化抑制剂在霍奇金淋巴瘤(HL)中的活性尚无任何了解。因此,我们评估了辛伐他汀和特异性异戊二烯化抑制剂的抗HL活性。2微摩尔的辛伐他汀通过消耗几种HL细胞系中的异戊二烯化底物诱导了半胱天冬酶相关的凋亡。此外,它在HL小鼠模型中有效抑制了肿瘤生长。由于异戊二烯化抑制剂FTI-277和GGTI-298对HL细胞也有效,我们得出结论,应在HL患者中评估他汀类药物和特异性异戊二烯化抑制剂。

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