Advancements in Gene-Based Therapeutic Angiogenesis for Chronic Limb-Threatening Ischemia.

IF 3.9 3区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Human gene therapy Pub Date : 2025-05-01 Epub Date: 2025-04-29 DOI:10.1089/hum.2024.245
Peng Wang, Xiao Di, Fengshi Li, Zhihua Rong, Wenzhuo Lian, Guoqiang Sun, ChangWei Liu, Leng Ni
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引用次数: 0

Abstract

The objective of this article is to summarize the research progress and discuss the current difficulties of gene-based therapeutic angiogenesis in lower limb ischemic diseases, so as to provide new research directions for the non-invasive treatment of lower limb ischemia. The basic and clinical trials of gene-based therapeutic angiogenesis in lower limb ischemia in recent years were read and reviewed. Growth factors such as vascular endothelial growth factor, hepatocyte growth factor, and fibroblast growth factor have been extensively studied for their application in lower limb ischemic diseases. However, clinical studies across various phases have shown inconsistent efficacy endpoints. The efficacy of gene therapy remains questionable. Before exploring efficient methods of delivering pro-angiogenic genes to ischemic tissues, clarification is needed regarding whether the goal of gene therapy is to simply promote collateral circulation or create a conducive tissue microenvironment for angiogenesis. In conclusion, pre-clinical and clinical studies have demonstrated the potential of therapeutic angiogenesis, but more systematic and comprehensive research is needed to explore safer, more effective, and cost-effective treatment methods.

基于基因的血管生成治疗慢性肢体缺血的进展。
本文旨在综述基于基因的治疗性血管生成在下肢缺血性疾病中的研究进展,并探讨目前存在的困难,为下肢缺血无创治疗提供新的研究方向。对近年来基于基因治疗下肢缺血血管生成的基础和临床试验进行了综述。血管内皮生长因子、肝细胞生长因子、成纤维细胞生长因子等生长因子在下肢缺血性疾病中的应用已被广泛研究。然而,不同阶段的临床研究显示了不一致的疗效终点。基因疗法的功效仍然值得怀疑。在探索将促血管生成基因传递到缺血组织的有效方法之前,需要澄清基因治疗的目标是简单地促进侧支循环还是为血管生成创造有利的组织微环境。总之,临床前和临床研究已经证明了治疗性血管生成的潜力,但需要更系统和全面的研究来探索更安全、更有效和更具成本效益的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human gene therapy
Human gene therapy 医学-生物工程与应用微生物
CiteScore
6.50
自引率
4.80%
发文量
131
审稿时长
4-8 weeks
期刊介绍: Human Gene Therapy is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes in-depth coverage of DNA, RNA, and cell therapies by delivering the latest breakthroughs in research and technologies. Human Gene Therapy provides a central forum for scientific and clinical information, including ethical, legal, regulatory, social, and commercial issues, which enables the advancement and progress of therapeutic procedures leading to improved patient outcomes, and ultimately, to curing diseases.
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