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首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >Arsenic trioxide induces apoptosis in B-cell chronic lymphocytic leukemic cells through down-regulation of survivin via the p53-dependent signaling pathway
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Arsenic trioxide induces apoptosis in B-cell chronic lymphocytic leukemic cells through down-regulation of survivin via the p53-dependent signaling pathway

机译:三氧化二砷通过依赖于p53的信号通路下调survivin诱导B细胞慢性淋巴细胞性白血病细胞凋亡

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摘要

Arsenic trioxide (As2O3) can induce apoptosis in many tumors. However, the associated mechanisms are not clearly understood. We found that As2O3 significantly inhibited the proliferation of WSU-CLL cells and induced apoptosis in dose- and time-dependent manners. WSU-CLL cells treated with 2μM As2O3 showed survivin down-regulation and p53 up-regulation. Survivin siRNA combined with As2O3 further inhibited the proliferation of WSU-CLL cells. p53 inhibition by siRNA prevented the down-regulation of survivin by As2O3 and prevented the As2O3-induced cytotoxicity of WSU-CLL cells. These results suggest that As2O3 may be of therapeutic value for chronic lymphocytic leukemia.
机译:三氧化二砷(As2O3)可以诱导许多肿瘤的凋亡。但是,相关机制尚不清楚。我们发现As2O3显着抑制WSU-CLL细胞的增殖,并以剂量​​和时间依赖性方式诱导细胞凋亡。用2μMAs2O3处理的WSU-CLL细胞显示survivin下调和p53上调。 Survivin siRNA联合As2O3进一步抑制WSU-CLL细胞的增殖。 siRNA对p53的抑制作用阻止了As2O3对survivin的下调,并阻止了As2O3诱导的WSU-CLL细胞的细胞毒性。这些结果表明As2O3可能对慢性淋巴细胞白血病具有治疗价值。

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