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Cucurbitacin B inhibits the stemness and metastatic abilities of NSCLC via downregulation of canonical Wnt/β-catenin signaling axis

机译:葫芦素B通过下调经典的Wnt /β-catenin信号传导轴抑制NSCLC的干细胞和转移能力

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摘要

Lack of effective anti-metastatic drugs creates a major hurdle for metastatic lung cancer therapy. For successful lung cancer treatment, there is a strong need of newer therapeutics with metastasis-inhibitory potential. In the present study, we determined the anti-metastatic and anti-angiogenic potential of a natural plant triterpenoid, Cucurbitacin B (CuB) against non-small cell lung cancer (NSCLC) both in vitro and in vivo. CuB demonstrated a strong anti-migratory and anti-invasive ability against metastatic NSCLC at nanomolar concentrations. CuB also showed significant tumor angiogenesis-inhibitory effects as evidenced by the inhibition of migratory, invasive and tube-forming capacities of human umbilical vein endothelial cells. CuB-mediated inhibition of angiogenesis was validated by the inhibition of pre-existing vasculature in chick embryo chorio-allantoic membrane and matrigel plugs. Similarly, CuB inhibited the migratory behavior of TGF-β1-induced experimental EMT model. The CuB-mediated inhibition of metastasis and angiogenesis was attributable to the downregulation of Wnt/β-catenin signaling axis, validated by siRNA-knockdown of Wnt3 and Wnt3a. The CuB-mediated downregulation of Wnt/β-catenin signaling was also validated using 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis model in vivo. Collectively, our findings suggest that CuB inhibited the metastatic abilities of NSCLC through the inhibition of Wnt/β-catenin signaling axis.
机译:缺乏有效的抗转移药物为转移性肺癌治疗创造了主要障碍。为了成功地治疗肺癌,强烈需要具有转移抑制潜力的新型治疗方法。在本研究中,我们在体外和体内测定了天然植物三萜类葫芦素B(CuB)对非小细胞肺癌(NSCLC)的抗转移和抗血管生成的潜力。 CuB对纳摩尔浓度的转移性NSCLC表现出强大的抗迁移和抗侵袭能力。 CuB还显示出显着的肿瘤血管生成抑制作用,如通过抑制人脐静脉内皮细胞的迁移,侵袭和管形成能力所证明的。 CuB介导的血管生成抑制作用已通过抑制鸡胚绒毛膜尿囊膜和基质胶塞中预先存在的脉管系统得到了证实。同样,CuB抑制了TGF-β1诱导的实验EMT模型的迁移行为。 CuB介导的转移和血管生成的抑制作用归因于Wnt /β-catenin信号转导轴的下调,这通过Wnt3和Wnt3a的siRNA敲低进行了验证。还使用4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)诱导的体内肺肿瘤发生模型验证了CuB介导的Wnt /β-catenin信号的下调。总体而言,我们的发现表明,CuB通过抑制Wnt /β-catenin信号传导轴来抑制NSCLC的转移能力。

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