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靶向血管内皮生长因子(VEGF)通路使脉管系统正常化:癌症治疗的新见解

Targeting VEGF pathway to normalize the vasculature: an emerging insight in cancer therapy.

作者信息

Wu Jing-Biao, Tang Ya-Ling, Liang Xin-Hua

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology (Sichuan University), Chengdu Sichuan, People's Republic of China,

出版信息

Onco Targets Ther. 2018 Oct 17;11:6901-6909. doi: 10.2147/OTT.S172042. eCollection 2018.

DOI:10.2147/OTT.S172042
PMID:30410348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6200071/
Abstract

Vascular normalization is a new concept of targeting angiogenesis to restore vessel structure and function and to increase blood perfusion and delivery of drugs. It has been confirmed that vascular normalization can decrease relapse and benefit other cancer therapy, including chemotherapy, radiotherapy, and immune cell therapy. The key point of this therapy is to inhibit pro-angiogenic factors and make it be balanced with anti-angiogenic factors, resulting in a mature and normal vessel characteristic. Vascular endothelial growth factor (VEGF) is a key player in the process of tumor angiogenesis, and inhibiting VEGF is a primary approach to tumor vessel normalization. Herein, we review newly uncovered mechanisms governing angiogenesis and vascular normalization of cancer and place emphasis on targeting VEGF pathway to normalize the vasculature. Also, important methods to depress VEGF pathway and make tumor vascular are discussed.

摘要

血管正常化是一种针对血管生成的新概念,旨在恢复血管结构和功能,增加血液灌注以及药物递送。已经证实,血管正常化可以减少复发,并使包括化疗、放疗和免疫细胞治疗在内的其他癌症治疗受益。这种治疗的关键在于抑制促血管生成因子,并使其与抗血管生成因子保持平衡,从而形成成熟且正常的血管特征。血管内皮生长因子(VEGF)是肿瘤血管生成过程中的关键因素,抑制VEGF是实现肿瘤血管正常化的主要方法。在此,我们综述了新发现的癌症血管生成和血管正常化调控机制,并着重介绍了靶向VEGF通路以使脉管系统正常化的方法。此外,还讨论了抑制VEGF通路和使肿瘤血管正常化的重要方法。

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Hypoxia inducible factor-1α/vascular endothelial growth factor signaling activation correlates with response to radiotherapy and its inhibition reduces hypoxia-induced angiogenesis in lung cancer.缺氧诱导因子-1α/血管内皮生长因子信号激活与放疗反应相关,其抑制可减少肺癌缺氧诱导的血管生成。
J Cell Biochem. 2018 Sep;119(9):7707-7718. doi: 10.1002/jcb.27120. Epub 2018 Jun 15.
2
Effects of siRNA-mediated HIF-1α gene silencing on angiogenesis in osteosarcoma.小干扰RNA介导的缺氧诱导因子-1α基因沉默对骨肉瘤血管生成的影响
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Anti-angiogenesis for cancer revisited: Is there a role for combinations with immunotherapy?
The Complex Tumor Microenvironment in Ovarian Cancer: Therapeutic Challenges and Opportunities.
卵巢癌中的复杂肿瘤微环境:治疗挑战与机遇。
Curr Oncol. 2024 Jul 1;31(7):3826-3844. doi: 10.3390/curroncol31070283.
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The disruptive role of LRG1 on the vasculature and perivascular microenvironment.LRG1对脉管系统和血管周围微环境的破坏作用。
Front Cardiovasc Med. 2024 Apr 30;11:1386177. doi: 10.3389/fcvm.2024.1386177. eCollection 2024.
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Gene therapy in glioblastoma multiforme: Can it be a role changer?多形性胶质母细胞瘤的基因治疗:它能否改变格局?
Heliyon. 2024 Feb 24;10(5):e27087. doi: 10.1016/j.heliyon.2024.e27087. eCollection 2024 Mar 15.
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Nature's Elixir for Cancer Treatment: Targeting Tumor-induced Neovascularization.癌症治疗的天然良方:靶向肿瘤诱导的血管生成
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Normalization of the tumor microenvironment by harnessing vascular and immune modulation to achieve enhanced cancer therapy.通过利用血管和免疫调节使肿瘤微环境正常化,以实现增强的癌症治疗。
Exp Mol Med. 2023 Nov;55(11):2308-2319. doi: 10.1038/s12276-023-01114-w. Epub 2023 Nov 1.
8
Analysis of microRNA expression in rat kidneys after VEGF inhibitor treatment under different degrees of hypoxia.分析不同程度缺氧条件下 VEGF 抑制剂治疗后大鼠肾脏中 microRNA 的表达。
Physiol Genomics. 2023 Nov 1;55(11):504-516. doi: 10.1152/physiolgenomics.00023.2023. Epub 2023 Aug 29.
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