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Tumour-endothelial cell communications: important and indispensable mediators of tumour angiogenesis

机译:肿瘤-内皮细胞通讯:肿瘤血管生成的重要和必不可少的介质。

摘要

Angiogenesis is an essential aspect of tumour growth and metastasis. Solid tumours cannot grow beyond 2-3 mm in diameter without inducing the formation of new blood vessels to support the energetic requirements of tumour cells. Angiogenesis is stimulated by cancer cells through a wide variety of cell-to-cell communication means. Cancer cells can induce endothelial changes by directly targeting cells via soluble factors, adhesion receptors, gap junctions and vesicles. They also can stimulate endothelial signaling pathways in an indirect way, e.g. by activating stromal cells, by secreting proteases into the extracellular space or even by changing the pH, temperature and availability of oxygen and nutrients. Anti-angiogenic drugs appear to be an effective cancer treatment in animal models but have been shown to have a limited effect in the long term. Resistance to anti-angiogenic therapies has been attributed to the ability of cancer cells to induce angiogenesis in a different way. We propose that cancer cells also change the way they communicate with endothelial cells in order to escape therapies that inhibit angiogenesis and that a better knowledge of this phenomenon will help us design more efficient drugs.
机译:血管生成是肿瘤生长和转移的重要方面。实体瘤的直径不能超过2-3 mm,而不会诱导新血管的形成来支持肿瘤细胞的能量需求。癌细胞通过多种细胞间通信手段刺激血管生成。癌细胞可以通过可溶性因子,粘附受体,间隙连接和囊泡直接靶向细胞,从而诱导内皮细胞的变化。它们还可以间接方式刺激内皮信号传导途径,例如通过刺激途径。通过激活基质细胞,通过将蛋白酶分泌到细胞外空间,甚至通过改变pH值,温度以及氧气和养分的利用率来实现。在动物模型中,抗血管生成药物似乎是一种有效的癌症治疗方法,但从长期来看,其作用有限。对抗血管生成疗法的抗性已归因于癌细胞以不同方式诱导血管生成的能力。我们建议癌细胞也改变它们与内皮细胞沟通的方式,以逃避抑制血管生成的疗法,并且更好地了解这种现象将有助于我们设计更有效的药物。

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