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Hypoxia, notch signalling, and prostate cancer

机译:缺氧,刻痕信号和前列腺癌

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摘要

The notch signalling pathway is involved in differentiation, proliferation, angiogenesis, vascular remodelling, and apoptosis. Deregulated expression of notch receptors, ligands, and targets is observed in many solid tumours, including prostate cancer. Hypoxia is a common feature of prostate tumours, leading to increased gene instability, reduced treatment response, and increased tumour aggressiveness. The notch signalling pathway is known to regulate vascular cell fate and is responsive to hypoxia-inducible factors. Evidence to date suggests similar, therapeutically exploitable, behaviour of notch-activated and hypoxic prostate cancer cells.
机译:Notch信号通路参与分化,增殖,血管生成,血管重塑和凋亡。在包括前列腺癌在内的许多实体瘤中均观察到Notch受体,配体和靶标的表达失调。缺氧是前列腺肿瘤的常见特征,导致基因不稳定性增加,治疗反应降低以及肿瘤侵袭性增加。已知Notch信号传导途径调节血管细胞命运并对缺氧诱导因子起反应。迄今为止的证据表明,陷波激活的和低氧的前列腺癌细胞具有相似的,可在治疗上利用的行为。

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