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Exosomes in Angiogenesis and Anti-angiogenic Therapy in Cancers

机译:癌症血管生成和抗血管生成治疗的外泌体

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摘要

Angiogenesis is the process through which new blood vessels are formed from pre-existing ones. Exosomes are involved in angiogenesis in cancer progression by transporting numerous pro-angiogenic biomolecules like vascular endothelial growth factor (VEGF), matrix metalloproteinases (MMPs), and microRNAs. Exosomes promote angiogenesis by suppressing expression of factor-inhibiting hypoxia-inducible factor 1 (HIF-1). Uptake of tumor-derived exosomes (TEX) by normal endothelial cells activates angiogenic signaling pathways in endothelial cells and stimulates new vessel formation. TEX-driven cross-talk of mesenchymal stem cells (MSCs) with immune cells blocks their anti-tumor activity. Effective inhibition of tumor angiogenesis may arrest tumor progression. Bevacizumab, a VEGF-specific antibody, was the first antiangiogenic agent to enter the clinic. The most important clinical problem associated with cancer therapy using VEGF- or VEFGR-targeting agents is drug resistance. Combined strategies based on angiogenesis inhibitors and immunotherapy effectively enhances therapies in various cancers, but effective treatment requires further research.
机译:血管生成是通过预先形成的新血管通过该过程。通过将血管内皮生长因子(VEGF)等血管内皮生长因子(VEGF),基质金属蛋白酶(MMP)和MicroRNA等血管生成的生物分子相同,外泌体参与癌症进展中的血管生成。外泌体通过抑制因子抑制缺氧诱导因子1(HIF-1)的表达而促进血管生成。通过正常内皮细胞吸收肿瘤衍生的外泌体(TEX)在内皮细胞中激活血管生成信号传导途径,并刺激新的血管形成。 Tex驱动的间充质干细胞(MSC)与免疫细胞阻断它们的抗肿瘤活性。有效抑制肿瘤血管生成可能会抑制肿瘤进展。 Bevacizumab,一种VEGF特异性抗体,是进入诊所的第一个抗血管生成剂。使用VEGF-或vefgR靶向剂与癌症治疗相关的最重要的临床问题是耐药性。基于血管生成抑制剂和免疫疗法的组合策略有效增强了各种癌症的疗法,但有效的治疗需要进一步研究。

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