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低剂量三氧化二砷联合阿克拉霉素A通过诱导凋亡协同增强对人急性髓性白血病细胞系的细胞毒性作用。

Low-dose arsenic trioxide combined with aclacinomycin A synergistically enhances the cytotoxic effect on human acute myelogenous leukemia cell lines by induction of apoptosis.

作者信息

Ye Yongbin, Xu Xiaojun, Zhang Mingwan, Qiu Dafa, Bai Xiaochun, Wang Jing, Weng Guangyang, Zhou Ruiqing, Guo Ziwen, He Huiqing, Yi Wenfang, He Xin, Guo Kunyuan

机构信息

a Department of Hematology , Zhujiang Hospital, Southern Medical University , Guangzhou , China.

b Department of Hematology , Zhongshan Hospital Affiliated to Sun Yat-Sen University , Zhongshan , China.

出版信息

Leuk Lymphoma. 2015;56(11):3159-67. doi: 10.3109/10428194.2015.1011155. Epub 2015 Jun 19.

Abstract

Acute myeloid leukemia (AML) is a common disorder in the elderly. Although remarkable progress has been made over recent decades, the outcome remains poor. Thus, the development of a more effective method to overcome this problem is necessary. In this study, we aimed to investigate the synergistic cytotoxic effect of low-dose arsenic trioxide (As2O3) combined with aclacinomycin A (ACM) on the human AML cell lines KG-1a and HL-60, and to clarify the underlying mechanism. Results showed that As2O3 combined with ACM exerted a synergistic cytotoxic effect by activation of the apoptosis pathway. Additionally, we found that the combination treatment decreased Bcl-2, c-IAP and XIAP expression but increased SMAC and caspase-3 expression more significantly than the single drug treatments. Furthermore, combination index (CI) values were < 1 in all matched combination groups. Additional evaluation of As2O3 combined with ACM as a potential therapeutic benefit for AML seems warranted.

摘要

急性髓系白血病(AML)是老年人中的常见疾病。尽管近几十年来已取得显著进展,但治疗结果仍然不佳。因此,有必要开发一种更有效的方法来克服这一问题。在本研究中,我们旨在研究低剂量三氧化二砷(As2O3)与阿克拉霉素A(ACM)联合应用对人AML细胞系KG-1a和HL-60的协同细胞毒性作用,并阐明其潜在机制。结果表明,As2O3与ACM联合应用通过激活凋亡途径发挥协同细胞毒性作用。此外,我们发现联合治疗比单药治疗更显著地降低了Bcl-2、c-IAP和XIAP的表达,但增加了SMAC和caspase-3的表达。此外,所有匹配联合组的联合指数(CI)值均<1。对As2O3与ACM联合应用作为AML潜在治疗益处进行进一步评估似乎是有必要的。

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