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Sonic Hedgehog Signaling Inhibition Provides Opportunities for Targeted Therapy by Sulforaphane in Regulating Pancreatic Cancer Stem Cell Self-Renewal

机译:音猬因子信号传导抑制提供用于靶向治疗由萝卜硫素机遇调节胰腺癌干细胞的自我更新

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摘要

Dysregulation of the sonic hedgehog (Shh) signaling pathway has been associated with cancer stem cells (CSC) and implicated in the initiation of pancreatic cancer. Pancreatic CSCs are rare tumor cells characterized by their ability to self-renew, and are responsible for tumor recurrence accompanied by resistance to current therapies. The lethality of these incurable, aggressive and invasive pancreatic tumors remains a daunting clinical challenge. Thus, the objective of this study was to investigate the role of Shh pathway in pancreatic cancer and to examine the molecular mechanisms by which sulforaphane (SFN), an active compound in cruciferous vegetables, inhibits self-renewal capacity of human pancreatic CSCs. Interestingly, we demonstrate here that Shh pathway is highly activated in pancreatic CSCs and plays important role in maintaining stemness by regulating the expression of stemness genes. Given the requirement for Hedgehog in pancreatic cancer, we investigated whether hedgehog blockade by SFN could target the stem cell population in pancreatic cancer. In an in vitro model, human pancreatic CSCs derived spheres were significantly inhibited on treatment with SFN, suggesting the clonogenic depletion of the CSCs. Interestingly, SFN inhibited the components of Shh pathway and Gli transcriptional activity. Interference of Shh-Gli signaling significantly blocked SFN-induced inhibitory effects demonstrating the requirement of an active pathway for the growth of pancreatic CSCs. SFN also inhibited downstream targets of Gli transcription by suppressing the expression of pluripotency maintaining factors (Nanog and Oct-4) as well as PDGFRα and Cyclin D1. Furthermore, SFN induced apoptosis by inhibition of BCL-2 and activation of caspases. Our data reveal the essential role of Shh-Gli signaling in controlling the characteristics of pancreatic CSCs. We propose that pancreatic cancer preventative effects of SFN may result from inhibition of the Shh pathway. Thus Sulforaphane potentially represents an inexpensive, safe and effective alternative for the management of pancreatic cancer.
机译:声音刺猬(Shh)信号通路的失调与癌症干细胞(CSC)有关,并与胰腺癌的发生有关。胰腺CSC是稀有的肿瘤细胞,其特征在于其自我更新的能力,并导致肿瘤复发以及对当前疗法的耐药性。这些无法治愈的,侵袭性和浸润性胰腺肿瘤的致死性仍然是一项艰巨的临床挑战。因此,本研究的目的是研究Shh途径在胰腺癌中的作用,并研究十字花科蔬菜中的活性化合物萝卜硫素(SFN)抑制人胰腺CSC自我更新能力的分子机制。有趣的是,我们在这里证明了Shh途径在胰腺CSC中被高度激活,并通过调节茎基因的表达在保持茎中起重要作用。考虑到胰腺癌需要刺猬,我们调查了SFN阻断刺猬是否可以靶向胰腺癌中的干细胞群体。在体外模型中,人胰腺CSCs衍生球在用SFN处理后受到显着抑制,表明CSCs的克隆形成耗竭。有趣的是,SFN抑制了Shh途径的成分和Gli转录活性。 Shh-Gli信号的干扰显着阻断了SFN诱导的抑制作用,表明需要胰腺CSCs生长的活性途径。 SFN还通过抑制多能维持因子(Nanog和Oct-4)以及PDGFRα和Cyclin D1的表达来抑制Gli转录的下游靶标。此外,SFN通过抑制BCL-2和激活胱天蛋白酶来诱导凋亡。我们的数据揭示了Shh-Gli信号在控制胰腺CSCs特性中的重要作用。我们提出SFN的胰腺癌预防作用可能是由于Shh途径的抑制。因此,萝卜硫烷可能代表着一种廉价,安全和有效的胰腺癌治疗替代方案。

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