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首页> 外文期刊>Journal of cellular biochemistry. >Tanshinone IIA inhibits breast cancer stem cells growth in vitro and in vivo through attenuation of IL-6/STAT3/NF-kB signaling pathways
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Tanshinone IIA inhibits breast cancer stem cells growth in vitro and in vivo through attenuation of IL-6/STAT3/NF-kB signaling pathways

机译:丹参酮IIA通过减弱IL-6 / STAT3 / NF-kB信号通路在体外和体内抑制乳腺癌干细胞的生长

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Cancer stem cells (CSCs) are maintained by inflammatory cytokines and signaling pathways. Tanshinone IIA (Tan-IIA) possesses anti-cancer and anti-inflammatory activities. The purpose of this study is to confirm the growth inhibition effect of Tan-IIA on human breast CSCs growth in vitro and in vivo and to explore the possible mechanism of its activity. Human breast CSCs were enriched and expanded under serum-free mammosphere culture condition, and identified through mammosphere formation, toluidine blue staining, immunofluorescence staining, and flow cytometry analysis of stemness markers of CD44/CD24 and ALDH, and tumorigenecity in vivo; the growth inhibition effect of Tan-IIA on human breast CSCs in vitro were tested by cell proliferation and mammosphere formation assays; inflammatory signaling pathway related protein expression in response to Tan-IIA, IL-6, STAT3, phospho-STAT3 (Tyr705), NF-κBp65 in cytoplasm and nucleus and cyclin D1 were evaluated with Western blotting; the growth inhibition effect of Tan-IIA on human breast CSCs growth were tested in vivo. A useful model of human breast CSCs for researching and developing the agents targeting CSCs was established. After Tan-IIA treatment, cell proliferation and mammosphere formation of CSCs were decreased significantly; the expression levels of IL-6, STAT3, phospho-STAT3 (Tyr705), NF-κBp65 in nucleus and cyclin D1 proteins were decreased significantly; the tumor growth and mean tumor weight were reduced significantly. Tan-IIA has the potential to target and kill CSCs, and can inhibit human breast CSCs growth both in vitro and in vivo through attenuation of IL-6/STAT3/NF-kB signaling pathways.
机译:癌症干细胞(CSC)通过炎症性细胞因子和信号通路来维持。丹参酮IIA(Tan-IIA)具有抗癌和抗炎活性。这项研究的目的是确认Tan-IIA对人乳腺CSCs体外和体内生长的抑制作用,并探讨其活性的可能机制。人乳腺干细胞在无血清乳球培养条件下富集和扩增,并通过乳球形成,甲苯胺蓝染色,免疫荧光染色,CD44 / CD24和ALDH的干性标记的流式细胞术分析以及体内肿瘤发生来鉴定。通过细胞增殖和乳球形成实验检测了Tan-IIA对人乳腺CSCs体外生长的抑制作用。用蛋白质印迹法评估细胞质和细胞核中Tan-IIA,IL-6,STAT3,磷酸STAT3(Tyr705),NF-κBp65应答的炎症信号通路相关蛋白表达;在体内测试了Tan-IIA对人乳腺CSCs生长的抑制作用。建立了用于研究和开发靶向CSC的药物的人乳腺CSC有用模型。 Tan-IIA处理后,CSCs的细胞增殖和乳球形成明显减少; IL-6,STAT3,磷酸化STAT3(Tyr705),NF-κBp65在细胞核和细胞周期蛋白D1蛋白中的表达水平明显降低;肿瘤生长和平均肿瘤重量均明显降低。 Tan-IIA具有靶向和杀死CSC的潜力,并且可以通过减弱IL-6 / STAT3 / NF-kB信号通路在体外和体内抑制人乳腺CSC的生长。

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