Laboratory of Geriatrics, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, China.
J Cell Biochem. 2013 Sep;114(9):2061-70. doi: 10.1002/jcb.24553.
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.
癌症干细胞(CSCs)由炎症细胞因子和信号通路维持。丹参酮 IIA(Tan-IIA)具有抗癌和抗炎活性。本研究旨在确认 Tan-IIA 在体外和体内对人乳腺癌 CSCs 生长的抑制作用,并探讨其活性的可能机制。人乳腺癌 CSCs 在无血清乳腺球体培养条件下富集和扩增,并通过乳腺球体形成、甲苯胺蓝染色、干细胞标志物 CD44/CD24 和 ALDH 的免疫荧光染色和流式细胞术分析以及体内致瘤性进行鉴定;通过细胞增殖和乳腺球体形成测定法检测 Tan-IIA 对体外人乳腺癌 CSCs 的生长抑制作用;用 Western blot 法评估 Tan-IIA 对 IL-6、STAT3、磷酸化 STAT3(Tyr705)、细胞质和细胞核中的 NF-κBp65 以及细胞周期蛋白 D1 的炎症信号通路相关蛋白表达的影响;在体内检测 Tan-IIA 对人乳腺癌 CSCs 生长的抑制作用。建立了一个用于研究和开发针对 CSCs 的药物的人乳腺癌 CSCs 有用模型。Tan-IIA 处理后,CSCs 的细胞增殖和乳腺球体形成明显减少;细胞核中 IL-6、STAT3、磷酸化 STAT3(Tyr705)、NF-κBp65 和细胞周期蛋白 D1 蛋白的表达水平明显降低;肿瘤生长和平均肿瘤重量明显减少。Tan-IIA 具有靶向和杀死 CSCs 的潜力,可通过减弱 IL-6/STAT3/NF-kB 信号通路来抑制体外和体内人乳腺癌 CSCs 的生长。