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Curcumin Combined with Thalidomide Reduces Expression of STAT3 and Bcl-xL , Leading to Apoptosis in Acute Myeloid Leukemia Cell Lines

机译:姜黄素结合沙利度胺减少了STAT3和BCL-XL的表达,导致急性髓性白血病细胞系中的细胞凋亡

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Introduction: Acute myeloid leukemia (AML) is a type of blood disorder that exhibits uncontrolled growth and reduced ability to undergo apoptosis. Signal transducer and activator of transcription 3 (STAT3) is a family member of transcription factors which promotes carcinogenesis in most human cancers. This effect on AML is accomplished through deregulation of several critical genes, such as B cell lymphoma-extra-large (BCL-XL) which is anti-apoptotic protein. The aim of this study was to evaluate the effect of curcumin (CUR) and thalidomide (THAL) on apoptosis induction and also the alteration of the mRNA expression level of STAT3 and BCL-XL mRNA on AML cell line compounds. Methods: The growth inhibitory effects of CUR and THAL and their combination were measured by MTT assay in U937 and KG-1 cell lines. The rates of apoptosis induction and cell cycle analysis were measured by concurrent staining with Annexin V and PI. The mRNA expression level of STAT3 and BCL-XL was evaluated by Real-Time PCR. Results: CUR inhibited proliferation and induced apoptosis in both KG-1 and U937 cells and this effect increased by combination with THAL. The expression level of STAT3 and BCL-XL was significantly down-regulated in KG-1 cells after treatment by CUR and THAL and their combination. Conclusion: Overall, our findings suggested that down-regulation of STAT3 and BCL-XL mRNA expression in response to CUR and THAL treatment lead to inhibition of cell growth and induction of apoptosis.
机译:简介:急性髓性白血病(AML)是一种血液障碍,其表现出不受控制的生长和降低的凋亡能力。转录3(Stat3)的信号传感器和活化剂是转录因子的家庭成员,其在大多数人类癌症中促进致癌物。通过对抗凋亡蛋白的B细胞淋巴瘤 - 超大(BCL-XL)的抗放松来完成对AML的这种对AML的影响。本研究的目的是评估姜黄素(Cur)和沙利度胺(Thal)对凋亡诱导的影响以及STAT3和BCL-XL mRNA对AML细胞系化合物的mRNA表达水平的改变。方法:通过U937和KG-1细胞系MTT测定法测定Cur和Thal及其组合的生长抑制作用。通过用膜蛋白V和PI并发染色测量凋亡诱导和细胞周期分析的速率。通过实时PCR评估STAT3和BCL-XL的mRNA表达水平。结果:Cur抑制kg-1和U937细胞中的增殖和诱导细胞凋亡,并且这种效果通过与Thal组合增加。通过Cur和Thal及其组合处理后,STAT3和BCL-XL的表达水平在KG-1细胞中显着下调。结论:总体而言,我们的研究结果表明,Dat 3和Bcl-XL mRNA表达的下调响应Cur和Thal治疗导致细胞生长和诱导细胞凋亡。

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