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急性髓性白血病诱导化疗患者的核因子-κB调节

Nuclear factor-kappaB modulation in patients undergoing induction chemotherapy for acute myelogenous leukemia.

作者信息

Strair Roger K, Gharibo Mecide, Schaar Dale, Rubin Arnold, Harrison Jonathan, Aisner Joseph, Lin Hsin-Ching, Lin Yong, Goodell Lauri, Anand Monika, Balsara Binaifer, Dudek Liesel, Rabson Arnold, Medina Daniel J

机构信息

Division of Medical Oncology, The Cancer Institute of New Jersey, New Brunswick, NJ 08901, USA.

出版信息

Clin Cancer Res. 2008 Nov 15;14(22):7564-8. doi: 10.1158/1078-0432.CCR-08-1390.

Abstract

PURPOSE

Nuclear factor-kappaB (NF-kappaB) is constitutively expressed in many acute myelogenous leukemia (AML) cells and AML stem cells. Ex vivo treatment of AML cells with inhibitors of NF-kappaB results in diminished AML cell survival and enhances the cytotoxic effects of chemotherapeutic agents. The purpose of this study was to determine if standard anti-inflammatory agents modulate AML cell nuclear NF-kappaB when administered in conjunction with induction chemotherapy.

EXPERIMENTAL DESIGN

Patients with newly diagnosed AML were treated with dexamethasone, choline magnesium trisalicylate, or both for 24 hours prior to and 24 hours following initiation of standard induction chemotherapy. AML cell nuclear NF-kappaB was measured at baseline, 24, and 48 hours.

RESULTS

Choline magnesium trisalicylate +/- dexamethasone decreased nuclear NF-kappaB, whereas dexamethasone alone was associated with an increase in nuclear NF-kappaB in AML cells.

CONCLUSIONS

These results show the feasibility of NF-kappaB modulation in conjunction with induction chemotherapy for patients with AML using inexpensive readily available medications. A follow-up study to determine the effects of NF-kappaB modulation on clinical end points is warranted.

摘要

目的

核因子-κB(NF-κB)在许多急性髓性白血病(AML)细胞和AML干细胞中组成性表达。用NF-κB抑制剂对AML细胞进行体外处理会导致AML细胞存活率降低,并增强化疗药物的细胞毒性作用。本研究的目的是确定标准抗炎药与诱导化疗联合使用时是否能调节AML细胞核中的NF-κB。

实验设计

新诊断的AML患者在开始标准诱导化疗前24小时和开始后24小时接受地塞米松、三水杨酸胆碱镁或两者联合治疗。在基线、24小时和48小时测量AML细胞核中的NF-κB。

结果

三水杨酸胆碱镁±地塞米松降低了细胞核中的NF-κB,而单独使用地塞米松与AML细胞中细胞核NF-κB的增加有关。

结论

这些结果表明,使用廉价且易于获得的药物,联合诱导化疗对AML患者进行NF-κB调节是可行的。有必要进行一项后续研究以确定NF-κB调节对临床终点的影响。

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