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Cardiovascular Gene Therapy: Past, Present, and Future.心血管基因治疗:过去、现在与未来。
Mol Ther. 2017 May 3;25(5):1095-1106. doi: 10.1016/j.ymthe.2017.03.027. Epub 2017 Apr 4.
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Fibroblast growth factor receptor 1 is a key inhibitor of TGFβ signaling in the endothelium.成纤维细胞生长因子受体1是内皮细胞中转化生长因子β信号传导的关键抑制剂。
Sci Signal. 2014 Sep 23;7(344):ra90. doi: 10.1126/scisignal.2005504.
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Endothelial cell FGF signaling is required for injury response but not for vascular homeostasis.内皮细胞的成纤维细胞生长因子信号传导是损伤反应所必需的,但不是血管稳态所必需的。
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Therapeutics targeting angiogenesis: genetics and epigenetics, extracellular miRNAs and signaling networks (Review).靶向血管生成的治疗方法:遗传学和表观遗传学、细胞外 miRNAs 和信号网络(综述)。
Int J Mol Med. 2013 Oct;32(4):763-7. doi: 10.3892/ijmm.2013.1444. Epub 2013 Jul 16.
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Hepatocyte growth factor inhibits lipopolysaccharide-induced oxidative stress via epithelial growth factor receptor degradation.肝细胞生长因子通过表皮生长因子受体降解抑制脂多糖诱导的氧化应激。
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Long-term follow-up evaluation of results from clinical trial using hepatocyte growth factor gene to treat severe peripheral arterial disease.应用肝细胞生长因子基因治疗严重外周动脉疾病的临床试验结果的长期随访评估。
Arterioscler Thromb Vasc Biol. 2012 Oct;32(10):2503-9. doi: 10.1161/ATVBAHA.111.244632. Epub 2012 Aug 16.
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Hypoxia-induced angiogenesis: good and evil.缺氧诱导的血管生成:利弊并存。
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Hypertension. 2012 May;59(5):958-65. doi: 10.1161/HYPERTENSIONAHA.111.183905. Epub 2012 Mar 5.
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针对外周动脉疾病血管生成的基因治疗策略。

Gene-Therapeutic Strategies Targeting Angiogenesis in Peripheral Artery Disease.

作者信息

Sanada Fumihiro, Taniyama Yoshiaki, Muratsu Jun, Otsu Rei, Shimizu Hideo, Rakugi Hiromi, Morishita Ryuichi

机构信息

Department of Clinical Gene Therapy, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

出版信息

Medicines (Basel). 2018 Mar 30;5(2):31. doi: 10.3390/medicines5020031.

DOI:10.3390/medicines5020031
PMID:29601487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6024305/
Abstract

The World Health Organization announced that cardiovascular disease is the number one cause of death globally, representing 31% of all global deaths. Coronary artery disease (CAD) affects approximately 5% of the US population aged 40 years and older. With an age-adjusted prevalence of approximately 12%, peripheral artery disease (PAD) affects at least 8 to 12 million Americans. Both CAD and PAD are caused by mainly atherosclerosis, the hardening and narrowing of arteries over the years by lipid deposition in the vascular bed. Despite the significant advances in interventions for revascularization and intensive medical care, patients with CAD or PAD who undergo percutaneous transluminal angioplasty have a persistent high rate of myocardial infarction, amputation, and death. Therefore, new therapeutic strategies are urgently needed for these patients. To overcome this unmet need, therapeutic angiogenesis using angiogenic growth factors has evolved in an attempt to stimulate the growth of new vasculature to compensate for tissue ischemia. After nearly 20 years of investigation, there is growing evidence of successful or unsuccessful gene therapy for ischemic heart and limb disease. This review will discuss basic and clinical data of therapeutic angiogenesis studies employing angiogenic growth factors for PAD patients and will draw conclusions on the basis of our current understanding of the biological processes of new vascularization.

摘要

世界卫生组织宣布,心血管疾病是全球头号死因,占全球总死亡人数的31%。冠状动脉疾病(CAD)影响着约5%的40岁及以上美国人口。外周动脉疾病(PAD)的年龄调整患病率约为12%,影响着至少800万至1200万美国人。CAD和PAD主要都是由动脉粥样硬化引起的,即多年来血管床中脂质沉积导致动脉变硬和变窄。尽管在血管再通干预和强化医疗护理方面取得了重大进展,但接受经皮腔内血管成形术的CAD或PAD患者仍持续存在较高的心肌梗死、截肢和死亡率。因此,这些患者迫切需要新的治疗策略。为了满足这一未得到满足的需求,利用血管生成生长因子进行治疗性血管生成已得到发展,试图刺激新血管生长以补偿组织缺血。经过近20年的研究,越来越多的证据表明基因治疗对缺血性心脏和肢体疾病有成功或不成功的案例。本综述将讨论针对PAD患者采用血管生成生长因子进行治疗性血管生成研究的基础和临床数据,并将根据我们目前对新血管形成生物学过程的理解得出结论。