首页> 美国卫生研究院文献>Asian Pacific Journal of Cancer Prevention : APJCP >OPN b and c Isoforms Doubtless Veto Anti-angiogenesis Effects of Curcumin in Combination with Conventional AML Regiment
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OPN b and c Isoforms Doubtless Veto Anti-angiogenesis Effects of Curcumin in Combination with Conventional AML Regiment

机译:OPN b和c同工型与常规AML结合无疑具有姜黄素的否决性抗血管生成作用

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摘要

Osteopontin (OPN) is an extracellular structural protein that is secreted by osteoblasts and hematopoietic cells. It suppresses the proliferation of hematopoietic stem and also plays an important role in promoting survival and drug resistance in leukemic stem cells (LSCs). Since the role of OPN isoforms in AML angiogenesis are remaining controversial, in the present study, we aimed to evaluate whether curcumin (CUR), as a known natural component with anti-angiogenesis effects, in a combination of AML conventional regiment has the potency to preclude induced anti-angiogenesis effects of OPN isoforms or not? Leukemia cells were treated with different concentration of CUR and AML conventional drugs alone and/or in combination with together to find effective doses and IC50 values. Percentages of apoptotic cells were evaluated by Annexin/PI staining and mRNA levels of OPN isoforms and AKT/ VEGF-A and VEGF-C/ STAT3/ β-catenin/ CXCR4/ IL-6/ KDR gene expression were investigated by Real Time-PCR method. Moreover, to confirm OPN gene expression data, we investigated the effect of simvastatin and OPN siRNA as an OPN inhibitor on the cell proliferation and induction of apoptosis in the indicated cell lines. Our data display that Ara-c (2μM and 1μM in KG-1 and U937 cell lines respectively), CUR (40μM in both cell lines), and also their combination significantly increased the percentage of apoptotic cells. Moreover, the mRNA level of OPN isoforms were down regulated in the KG-1and U937 cell lines treated with Ara-c while, upregulated in KG-1and U937 cell lines treated with CUR and its combination. Our results suggest that despite anti-angiogenesis effects of CUR, AML cells probably evade from anti-angiogenesis effects of CUR via induction of OPN b and c isoform and related molecular pathways.
机译:骨桥蛋白(OPN)是成骨细胞和造血细胞分泌的一种细胞外结构蛋白。它抑制造血干细胞的增殖,并且在促进白血病干细胞(LSCs)的存活和耐药性中起重要作用。由于OPN亚型在AML血管生成中的作用仍然存在争议,因此在本研究中,我们旨在评估姜黄素(CUR)作为已知的具有抗血管生成作用的天然成分,在AML常规治疗方案的组合中是否具有是否可以排除OPN亚型的诱导抗血管生成作用?单独和/或组合使用不同浓度的CUR和AML常规药物治疗白血病细胞,以找到有效剂量和IC50值。通过膜联蛋白/ PI染色评估凋亡细胞的百分比,并通过实时荧光定量PCR检测OPN亚型和AKT / VEGF-A和VEGF-C / STAT3 /β-catenin/ CXCR4 / IL-6 / KDR基因表达的mRNA水平。方法。此外,为证实OPN基因表达数据,我们研究了辛伐他汀和OPN siRNA作为OPN抑制剂对所示细胞系中细胞增殖和凋亡诱导的影响。我们的数据显示,Ara-c(分别在KG-1和U937细胞系中为2μM和1μM),CUR(在两种细胞系中为40μM)及其组合显着增加了凋亡细胞的百分比。此外,在Ara-c处理的KG-1和U937细胞系中OPN亚型的mRNA水平下调,而在用CUR及其组合处理的KG-1和U937细胞系中OPN亚型的mRNA水平上调。我们的结果表明,尽管CUR具有抗血管生成作用,但AML细胞可能通过诱导OPN b和c同工型及相关分子途径而逃避了CUR的抗血管生成作用。

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