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Hypoxia inducible factors in the tumor microenvironment as therapeutic targets of cancer stem cells

机译:肿瘤微环境中缺氧诱导因子作为癌症干细胞的治疗靶标

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Cancer stem cells (CSC) constitute a small area of the tumor mass and are characterized by self-renewal, differentiation and the ability to promote the development of secondary chemo-resistant tumors. Self-renewal of CSCs is regulated through various signaling pathways including Hedgehog, Notch, and Wnt/beta-catenin pathways. A few surface markers have been identified, which provide a means of targeting CSCs according to tumor type. Depending on the proximity of CSCs to the tumor hypoxic niche, hypoxia-inducible factors (HIFs) can play a critical role in modulating several CSC-related characteristics. For instance, the upregulation of HIF-1 and HIF-2 at tumor sites, which correlates with the expansion of CSCs and poor cancer prognosis, has been demonstrated. In this review, we will discuss the mechanisms by which hypoxia enhances the development of CSCs in the tumor microenvironment. Targeting HIFs in combination with other common therapeutics is pre-requisite for effective eradication of CSCs.
机译:癌症干细胞(CSC)构成肿瘤质量的小面积,其特征在于自我更新,分化和促进次级化学抗性肿瘤的发育的能力。通过包括刺猬,缺口和WNT /β-连环蛋白途径的各种信号通路来调节CSC的自我更新。已经鉴定了几种表面标志物,其提供了根据肿瘤型靶向CSC的方法。根据CSCs对肿瘤缺氧性缺氧的邻近,缺氧诱导因子(HIF)可以在调节几个CSC相关特征方面发挥关键作用。例如,已经证明了肿瘤部位的HIF-1和HIF-2的上调,其与CSCs扩张和癌症预后差的膨胀相关。在本综述中,我们将讨论缺氧增强肿瘤微环境中CSC的机制。靶向HIF与其他​​常见治疗剂的组合是有效消除CSC的先决条件。

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