Lee Chunsik, Kim Myung-Jin, Kumar Anil, Lee Han-Woong, Yang Yunlong, Kim Yonghwan
Department of R&D, GEMCRO Inc, Seoul, Republic of Korea.
Department of Biological Sciences and Research Institute of Women's Health, Sookmyung Women's University, Seoul, Republic of Korea.
Signal Transduct Target Ther. 2025 May 19;10(1):170. doi: 10.1038/s41392-025-02249-0.
Vascular endothelial growth factor (VEGF) signaling is a critical regulator of vasculogenesis, angiogenesis, and lymphangiogenesis, processes that are vital for the development of vascular and lymphatic systems, tissue repair, and the maintenance of homeostasis. VEGF ligands and their receptors orchestrate endothelial cell proliferation, migration, and survival, playing a pivotal role in dynamic vascular remodeling. Dysregulated VEGF signaling drives diverse pathological conditions, including tumor angiogenesis, cardiovascular diseases, and ocular disorders. Excessive VEGF activity promotes tumor growth, invasion, and metastasis, while insufficient signaling contributes to impaired wound healing and ischemic diseases. VEGF-targeted therapies, such as monoclonal antibodies and tyrosine kinase inhibitors, have revolutionized the treatment of diseases involving pathological angiogenesis, offering significant clinical benefits in oncology and ophthalmology. These therapies inhibit angiogenesis and slow disease progression, but they often face challenges such as therapeutic resistance, suboptimal efficacy, and adverse effects. To further explore these issues, this review provides a comprehensive overview of VEGF ligands and receptors, elucidating their molecular mechanisms and regulatory networks. It evaluates the latest progress in VEGF-targeted therapies and examines strategies to address current challenges, such as resistance mechanisms. Moreover, the discussion includes emerging therapeutic strategies such as innovative drug delivery systems and combination therapies, highlighting the continuous efforts to improve the effectiveness and safety of VEGF-targeted treatments. This review highlights the translational potential of recent discoveries in VEGF biology for improving patient outcomes.
血管内皮生长因子(VEGF)信号传导是血管生成、血管新生和淋巴管生成的关键调节因子,这些过程对于血管和淋巴系统的发育、组织修复以及体内平衡的维持至关重要。VEGF配体及其受体协调内皮细胞的增殖、迁移和存活,在动态血管重塑中起关键作用。VEGF信号传导失调会引发多种病理状况,包括肿瘤血管生成、心血管疾病和眼部疾病。VEGF活性过高会促进肿瘤生长、侵袭和转移,而信号传导不足则会导致伤口愈合受损和缺血性疾病。针对VEGF的疗法,如单克隆抗体和酪氨酸激酶抑制剂,彻底改变了涉及病理性血管生成疾病的治疗方式,在肿瘤学和眼科领域带来了显著的临床益处。这些疗法抑制血管生成并减缓疾病进展,但它们常常面临诸如治疗抗性、疗效欠佳和不良反应等挑战。为了进一步探讨这些问题,本综述全面概述了VEGF配体和受体,阐明了它们的分子机制和调控网络。它评估了VEGF靶向治疗的最新进展,并研究应对当前挑战(如抗性机制)的策略。此外,讨论还包括新兴的治疗策略,如创新的药物递送系统和联合疗法,强调了为提高VEGF靶向治疗的有效性和安全性而持续做出的努力。本综述突出了VEGF生物学领域近期发现对于改善患者预后的转化潜力。