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蛋白酶体抑制剂可消除白血病细胞在抗微管药物诱导的凋亡过程中半胱天冬酶激活下游的细胞死亡。

Proteasome inhibitors abolish cell death downstream of caspase activation during anti-microtubule drug-induced apoptosis in leukemia cells.

作者信息

Nagy Katalin, Petak Istvan, Imre Gergely, Barna Gabor, Gezane-Csorba Maria, Sebestyen Anna, Houghton Janet A, Mihalik Rudolf, Kopper Laszlo

机构信息

First Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

出版信息

Anticancer Res. 2005 Sep-Oct;25(5):3321-6.

Abstract

PURPOSE

Anti-microtubule drugs and proteasome inhibitors are currently among the most intensively studied anti-tumor agents, however little is known about their pharmacological interactions at the cellular level.

MATERIALS AND METHODS

The human promyelocytic leukemia cell line, HL-60, was exposed to nocodazole or etoposide in combination with proteasome or caspase inhibitors. Apoptotic cell death was detected by flow cytometry as sub-G1 population. Caspase and proteasome activities were monitored by the fluorogenic substrates Ac-DEVD-AMC and Suc-LLVY-AMC, respectively, in cell lysate. Heat shock protein 70 (HSP70) expression was determined by Western blotting.

RESULTS

Nocodazole, a microtubule inhibitor, induced caspase-dependent apoptosis in the HL-60 cell line. At sub-cytotoxic concentrations, proteasome inhibitors, including MG-132 or clasto-beta-lactone, decreased nocodazole-induced apoptotic DNA fragmentation without affecting the induction of caspase-3 activity. In contrast, MG-132 decreased both DNA fragmentation and caspase activation induced by etoposide, a topoisomerase-II inhibitor. HSP70 had previously been found to inhibit apoptosis independently from caspase activation. In this study, MG-132 up-regulated HSP70 protein expression, both in the presence or absence of nocodazole.

CONCLUSION

Proteasome inhibitors decreased anti-microtubule agent-induced apoptotic DNA fragmentation downstream of caspase-3 activation, possibly due to increased HSP70 expression. The results indicate that combination treatment with these novel anti-tumor agents in leukemia requires careful evaluation of their molecular interaction at the level of apoptosis induction.

摘要

目的

抗微管药物和蛋白酶体抑制剂是目前研究最为深入的抗肿瘤药物,但人们对它们在细胞水平上的药理相互作用知之甚少。

材料与方法

将人早幼粒细胞白血病细胞系HL-60暴露于诺考达唑或依托泊苷,并联合蛋白酶体或半胱天冬酶抑制剂。通过流式细胞术检测凋亡细胞死亡,以亚G1期细胞群体表示。分别用荧光底物Ac-DEVD-AMC和Suc-LLVY-AMC监测细胞裂解物中的半胱天冬酶和蛋白酶体活性。通过蛋白质印迹法测定热休克蛋白70(HSP70)的表达。

结果

微管抑制剂诺考达唑在HL-60细胞系中诱导半胱天冬酶依赖性凋亡。在亚细胞毒性浓度下,包括MG-132或克拉托-β-内酯在内的蛋白酶体抑制剂可减少诺考达唑诱导的凋亡DNA片段化,而不影响半胱天冬酶-3活性的诱导。相反,MG-132可减少拓扑异构酶-II抑制剂依托泊苷诱导的DNA片段化和半胱天冬酶激活。此前已发现HSP70可独立于半胱天冬酶激活抑制凋亡。在本研究中,无论有无诺考达唑,MG-132均可上调HSP70蛋白表达。

结论

蛋白酶体抑制剂可在半胱天冬酶-3激活下游减少抗微管药物诱导的凋亡DNA片段化,这可能是由于HSP70表达增加所致。结果表明,在白血病中联合使用这些新型抗肿瘤药物需要仔细评估它们在凋亡诱导水平上的分子相互作用。

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