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BAG3基因沉默使白血病细胞对硼替佐米诱导的凋亡敏感。

BAG3 gene silencing sensitizes leukemic cells to Bortezomib-induced apoptosis.

作者信息

Liu Peng, Xu Bei, Li Jianyong, Lu Hua

机构信息

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, People's Republic of China.

出版信息

FEBS Lett. 2009 Jan 22;583(2):401-6. doi: 10.1016/j.febslet.2008.12.032. Epub 2008 Dec 25.

Abstract

Proteasome inhibition has emerged as a powerful option for the treatment of a number of malignancies including leukemias. However, Bortezomib showed limited single-agent activity for patients with leukemia. Here, we report for the first time that Bortezomib up-regulated a novel antiapoptotic protein, BAG3, in human leukemic cells. BAG3 gene knockdown with shRNA greatly potentiated the generation of apoptosis by Bortezomib in leukemia cells. Furthermore, BAG3 silencing enhanced the antitumor activity of Bortezomib dramatically in a nude mouse model. Our results indicate that knocking down BAG3 gene is a promising new approach to enhance the therapeutic potency of Bortezomib in leukemia.

摘要

蛋白酶体抑制已成为治疗包括白血病在内的多种恶性肿瘤的有力选择。然而,硼替佐米对白血病患者的单药活性有限。在此,我们首次报道硼替佐米在人白血病细胞中上调了一种新型抗凋亡蛋白BAG3。用短发夹RNA敲低BAG3基因极大地增强了硼替佐米在白血病细胞中诱导凋亡的作用。此外,在裸鼠模型中,BAG3沉默显著增强了硼替佐米的抗肿瘤活性。我们的结果表明,敲低BAG3基因是增强硼替佐米治疗白血病疗效的一种有前景的新方法。

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