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肿瘤-内皮细胞通讯:肿瘤血管生成的重要且不可或缺的介质

Tumour-Endothelial Cell Communications: Important and Indispensable Mediators of Tumour Angiogenesis.

作者信息

Lopes-Bastos Bruno Miguel, Jiang Wen G, Cai Jun

机构信息

Cardiff China Medical Research Collaborative, Institute of Cancer & Genetics, School of Medicine, Cardiff University, Cardiff, U.K.

出版信息

Anticancer Res. 2016 Mar;36(3):1119-26.

Abstract

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.

摘要

血管生成是肿瘤生长和转移的一个重要方面。实体瘤如果不诱导新血管形成以满足肿瘤细胞的能量需求,直径就无法超过2 - 3毫米。癌细胞通过多种细胞间通讯方式刺激血管生成。癌细胞可通过可溶性因子、黏附受体、间隙连接和囊泡直接作用于细胞,从而诱导内皮细胞发生变化。它们还能以间接方式刺激内皮细胞信号通路,例如通过激活基质细胞、向细胞外空间分泌蛋白酶,甚至通过改变pH值、温度以及氧气和营养物质的供应。抗血管生成药物在动物模型中似乎是一种有效的癌症治疗方法,但长期来看效果有限。对抗血管生成疗法的耐药性归因于癌细胞以不同方式诱导血管生成的能力。我们认为,癌细胞还会改变它们与内皮细胞的通讯方式,以逃避抑制血管生成的疗法,更好地了解这一现象将有助于我们设计出更有效的药物。

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