Rüegg Curzio, Dormond Olivier, Mariotti Agnese
Centre Pluridisciplinaire d'Oncologie, University of Lausanne Medical School, CH-1011 Lausanne, Switzerland.
Biochim Biophys Acta. 2004 Mar 4;1654(1):51-67. doi: 10.1016/j.bbcan.2003.09.003.
Vascular integrins are essential regulators and mediators of physiological and pathological angiogenesis, including tumor angiogenesis. Integrins provide the physical interaction with the extracellular matrix (ECM) necessary for cell adhesion, migration and positioning, and induce signaling events essential for cell survival, proliferation and differentiation. Integrins preferentially expressed on neovascular endothelial cells, such as alphaVbeta3 and alpha5beta1, are considered as relevant targets for anti-angiogenic therapies. Anti-integrin antibodies and small molecular integrin inhibitors suppress angiogenesis and tumor progression in many animal models, and are currently tested in clinical trials as anti-angiogenic agents. Cyclooxygense-2 (COX-2), a key enzyme in the synthesis of prostaglandins and thromboxans, is highly up-regulated in tumor cells, stromal cells and angiogenic endothelial cells during tumor progression. Recent experiments have demonstrated that COX-2 promotes tumor angiogenesis. Chronic intake of nonsteroidal anti-inflammatory drugs and COX-2 inhibitors significantly reduces the risk of cancer development, and this effect may be due, at least in part, to the inhibition of tumor angiogenesis. Endothelial cell COX-2 promotes integrin alphaVbeta3-mediated endothelial cell adhesion, spreading, migration and angiogenesis through the prostaglandin-cAMP-PKA-dependent activation of the small GTPase Rac. In this article, we review the role of integrins and COX-2 in angiogenesis, their cross talk, and discuss implications relevant to their targeting to suppress tumor angiogenesis.
血管整合素是生理性和病理性血管生成(包括肿瘤血管生成)的重要调节因子和介质。整合素提供与细胞外基质(ECM)的物理相互作用,这对于细胞黏附、迁移和定位是必需的,并诱导对细胞存活、增殖和分化至关重要的信号事件。优先在新生血管内皮细胞上表达的整合素,如αVβ3和α5β1,被认为是抗血管生成治疗的相关靶点。抗整合素抗体和小分子整合素抑制剂在许多动物模型中可抑制血管生成和肿瘤进展,目前作为抗血管生成药物正在进行临床试验。环氧化酶-2(COX-2)是前列腺素和血栓素合成中的关键酶,在肿瘤进展过程中,在肿瘤细胞、基质细胞和血管生成内皮细胞中高度上调。最近的实验表明,COX-2促进肿瘤血管生成。长期摄入非甾体抗炎药和COX-2抑制剂可显著降低癌症发生风险,这种作用可能至少部分归因于对肿瘤血管生成的抑制。内皮细胞COX-2通过小GTP酶Rac的前列腺素-cAMP-PKA依赖性激活,促进整合素αVβ3介导的内皮细胞黏附、铺展、迁移和血管生成。在本文中,我们综述了整合素和COX-2在血管生成中的作用、它们的相互作用,并讨论了针对它们以抑制肿瘤血管生成的相关意义。
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